بورتزومیب
Bortezomib (Velcade)
بورتزومیب

نام ژنریک

Bortezomib

شکل دارویی

اشكال دارويي:


Injection, Powder, Lyophilized : 3.5 mg


موارد مصرف

موارد و مقدار مصرف


درمان مالتيپل ميلوما در بيماراني كه علي‌رغم يك دوره درمان قبلي همچنان بيماري آنها پيشرفت مي‌كند.


بزرگسالان: mg/m2 1.3 به صورت بولوس وريدي دو بار در هفته براي دو هفته (روزهاي 1، 4، 8 و 11) تجويز شده و سپس يك دوره 10 روزه (روزهاي 12 تا 21) استراحت درماني داده مي‌شود. مجموعه اين سه هفته يك سيكل درماني محسوب مي‌شود. در مواردي كه بيش از 8 سيكل درماني مورد نياز است، دارو به صورت هفتگي براي 4 هفته (روزهاي 1، 8، 15 و 22) تجويز
شده و سپس يك دوره 13 روزه (روزهاي 23 تا 35) استراحت درماني داده مي‌شود. دوزهاي پشت سر هم دارو با فاصله حداقل 72 ساعت از هم تجويز شوند.


تنظيم دوز: در صورت بروز سميت غير خوني درجه 3 يا خوني درجه 4 (به جز نوروپاتي) دارو را متوقف كنيد. زماني كه عوارض دارو برطرف شد، با مقادير 25% كمتر دارو را شروع كنيد. در صورت بروز دردهاي نوروپاتيك يا نوروپاتي محيطي طبق جدول زير دوز دارو را تنظيم كنيد:





































شدت نوروپاتي





دوز




درجه يك (پارستزي، كاهش رفلكسR04;ها يا هر دو، بدون درد يا
كاهش عملكرد)




عدم تغيير




درجه يك با درد يا درجه دو (اختلال در عملكرد به جز
فعاليتR04;هاي روزمره)




دوز را به


mg/m



1 كاهش دهيد.




درجه دو با درد يا درجه سه (اختلال در انجام فعاليتR04;هاي
روزمره)




دارو را تا برطرف شدن عوارض متوقف كرده و سپس به ميزان


mg/m


0.7

هفتگي شروع كنيد.




درجه چهار (آسيب دائم عملكرد حسي كه باعث اختلال در
عملكرد شود)




دارو را متوقف كنيد.





موارد منع مصرف

موارد منع مصرف و احتياط


موارد منع مصرف: حساسيت به دارو، boron، مانتيول يا ديگر تركيبات فرمولاسيون.


موارد احتياط: دارو مي‌تواند باعث نوتروپني و ترومبوسيتوپني شديد مي‌شود. احتمال اين عارضه در پلاكت كمتر از 75000 افزايش مي‌يابد،‌ در صورت پلاكت كمتر از 25000 دارو متوقف شود. خونريزي (گوارشي و مغزي) به دليل پلاكت پايين گزارش شده است. دارو همچنين باعث افت فشارخون مي‌شود؛ در بيماران با سابقه دهيدراتاسيون، سابقه سنكوپ، با احتياط به كار مي‌رود. دارو باعث بدتر شدن نارسايي قلبي مي‌شود،‌ در اين گروه از بيماران نيز با احتياط به كار رود. طولاني شدن فاصله QT نيز به دنبال مصرف دارو گزارش شده است.


فعال شدن مجدد هرپس (زونا و آبله‌مرغان) به دنبال مصرف دارو گزارش شده است، به صورت پروفيلاكسي از داروهاي ضد ويروس استفاده شود.


دارو باعث ايجاد نوروپاتي محيطي (اغلب حسي ولي گاهي حسي ـ حركتي) مي‌شود.


مصرف قبلي يا همزمان داروهاي نوروتوكسيك باعث تشديد اين عارضه مي‌شود.


اختلالات ريوي شامل پنومونيت، پنوموني بينابيني، انفيلتراسيون ريوي و سندرم لكوآنسفالوپاتي خلفي برگشت‌پذير (RPLS) به ندرت به دنبال مصرف اين دارو گزارش شده است. علائم اين سندرم شامل كانفيوژن، سردرد، افزايش فشارخون، لتارژي، تشنج، كوري يا ديگر تغييرات بينايي و اختلالات نورولوژيك مي‌باشد. در صورت بروز اين سندرم مصرف دارو قطع شود.


سندرم ليزتومور به دنبال مصرف دارو گزارش شده است. مواردي از افت يا افزايش قندخون در بيماراني كه داروهاي كاهنده قندخون دريافت مي‌كنند، گزارش شده است. تنظيم دوز داروها در اين مورد لازم است.


در بيماران با نارسايي كبدي يا كليوي با احتياط تجويز شود.


عوارض جانبی دارو

عوارض جانبي


اعصاب مرکزي: اضطراب، ضعف، سرگيجه، ديس‌استزي، تب، سردرد، بي‌خوابي، پارستزي، نوروپاتي محيطي، لرز.


قلبي ـ عروقي: ادم، افت فشارخون.


چشم، گوش، حلق و بيني: تاري ديد.


دستگاه گوارش: دردهاي شكمي، يبوست، كاهش اشتها، اسهال، سوء‌هاضمه، تغيير طعم دهان، تهوع، استفراغ.


خوني: آنمي، نوتروپني، ترومبوسيتوپني.


عضلاني ـ اسكلتي: آرترالژي، درد كمر، دردهاي استخواني، كرامپ‌هاي عضلاني، ميالژي.


تنفسي: سرفه، تنگي نفس، پنوموني، عفونت‌هاي دستگاه تنفس فوقاني.


پوست: راش، خارش.


ساير عوارض: دهيدراتاسيون، زونا، پيركسي.


مسموميت و درمان


موردي گزارش نشده است. در صورت بروز مسموميت، علائم حياتي بيمار را مانتيور كنيد. فشارخون و دماي بدن بيمار را كنترل كنيد.


موارد قابل توجه

-

تداخل دارویی

تداخل دارويي


مصرف همزمان با ساير داروهاي كاهنده فشارخون باعث افت فشارخون مي‌شود.


مصرف همزمان با مهار كننده‌ها يا القاء كننده‌هاي آنزيم CYP3A4 باعث افزايش عوارض يا كاهش اثربخشي دارو مي‌شود.


مصرف همزمان با داروهاي خوراكي ضد ديابت باعث افت يا افزايش قندخون مي‌شود.


داروهاي ايجاد كننده نوروپاتي محيطي مانند آميودارون،‌ ضد ويروس‌ها، ايزونيازيد، نيتروفورانتوئين، استاتين‌ها در مصرف همزمان با اين دارو باعث تشديد نوروپاتي مي‌شوند.


مکانیزم اثر

تداخل دارويي


مصرف همزمان با ساير داروهاي كاهنده فشارخون باعث افت فشارخون مي‌شود.


مصرف همزمان با مهار كننده‌ها يا القاء كننده‌هاي آنزيم CYP3A4 باعث افزايش عوارض يا كاهش اثربخشي دارو مي‌شود.


مصرف همزمان با داروهاي خوراكي ضد ديابت باعث افت يا افزايش قندخون مي‌شود.


داروهاي ايجاد كننده نوروپاتي محيطي مانند آميودارون،‌ ضد ويروس‌ها، ايزونيازيد، نيتروفورانتوئين، استاتين‌ها در مصرف همزمان با اين دارو باعث تشديد نوروپاتي مي‌شوند.


فارماكوكینتیك

فارماكوكينتيك


جذب: اطلاعاتي در دست نيست.


پخش: دارو به ميزان 83% به پروتئين‌هاي پلاسما متصل مي‌شود.


متابوليسم: دارو در كبد توسط سيتوكروم P450 متابوليزه مي‌شود.


دفع: نيمه‌ عمر دارو در بدن 9 تا 15 ساعت است.

سایر اطلاعات

طبقه‌بندي فارماكولوژيك: مهار كننده پروتئوزوم


طبقه‌بندي درماني : ضد نئوپلاسم


طبقه‌بندي مصرف در بارداري: رده D


نام‌هاي تجاري: Velcade


ملاحظات اختصاصي


1- تهيه دارو با احتياط و تحت شرايط استريل انجام گيرد. براي جلوگيري از تماس پوستي از دستكش استفاده شود.


2- ويال حاوي دارو با 5/3 ميلي‌ليتر نرمال‌سالين رقيق شده و در عرض 8 ساعت از تهيه به صورت بولوس وريدي تجويز شود.


3- علائم نوروپاتي مانند احساس سوزش، هايپراستزي، هايپواستزي، پارستزي و دردهاي نوروپاتيك را مانيتور كنيد.


4- بيماراني كه علائم جديد يا پيشرونده نوروپاتي را پيدا مي‌كنند، نياز به تغيير دوز بورتزوميب دارند.


5- به دليل ايجاد تهوع، استفراغ، اسهال و يبوست به دنبال تجويز دارو، بيماران ممكن است، نياز به داروي ضد استفراغ، ضد اسهال يا هر دو داشته باشند.


6- جهت پيشگيري از دهيدراتاسيون جايگزيني مايع و الكتروليت‌ها صورت گيرد.


7- در بيماران با نارسايي كبدي يا كليوي، عوارض دارو را به دقت مانيتور كنيد.


8- جهت كنترل افت فشارخون وضعيتي ناشي از دارو، دوز داروهاي ضد فشارخون را تنظيم كرده و از مايعات و در صورت لزوم مينرالوكورتيكوئيدها استفاده كنيد.


9- به دليل بروز ترومبوسيتوپني ناشي از دارو، CBC و تعداد پلاكت بيمار را در طي درمان به خصوص در روز يازدهم مانيتور كنيد.


10- داروي رقيق شده تا 3 ساعت در دماي 15 تا 30 درجه سانتي‌گراد قابل نگهداري است، كل زمان نگهداري داروي رقيق شده در شرايط عادي نبايد از 8 ساعت تجاوز كند.


11- ويالهاي رقيق نشده دارو در دماي اتاق و دور از نور نگهداري شوند.


نكات قابل توصيه به بيمار


1- علائم جديد يا پيشرونده نوروپاتي را گزارش كنيد.


2- خانمها در طي مصرف دارو از روشهاي پيشگيري از بارداري استفاده كرد و از شيردهي به نوزاد خودداري كنند.


3- به بيمار آموزش دهيد كه از دهيدراتاسيون پرهيز كرده و علائم سرگيجه، سبكي سر را گزارش دهد.


4- به دليل ايجاد احساس خستگي، سرگيجه، غش كردن، سبكي سر،‌ دوبيني يا تاري ديد، طي مصرف دارو احتياطات كافي به عمل آيد.


مصرف در سالمندان: اطلاعات مصرف دارو در اين گروه سني محدود است. عوارض جانبي ناشي از دارو را به دقت مانيتور كنيد.


مصرف در كودكان: ايمني و اثربخشي دارو در اين گروه سني اثبات نشده است.


مصرف در شيردهي: ترشح دارو در شير مشخص نيست. ضمن مصرف دارو، شيردهي صورت نگيرد.


مصرف در بارداري: ايمني و اثربخشي دارو اثبات نشده است. بهتر است ضمن مصرف دارو،‌ بارداري صورت نگيرد.


اثر بر آزمايشهاي تشخيصي


دارو باعث كاهش هموگلوبين، نوتروفيل و پلاكت‌ها مي‌شود.


Bortezomib (Velcade)

VELCADE ®
(bortezomib)

DRUG DESCRIPTION

VELCADE® (bortezomib) for Injection is an antineoplastic agent available for intravenous injection or subcutaneous use. Each single use vial contains 3.5 mg of bortezomib as a sterile lyophilized powder. Inactive ingredient: 35 mg mannitol, USP.

Bortezomib is a modified dipeptidyl boronic acid. The product is provided as a mannitol boronic ester which, in reconstituted form, consists of the mannitol ester in equilibrium with its hydrolysis product, the monomeric boronic acid. The drug substance exists in its cyclic anhydride form as a trimeric boroxine.

The chemical name for bortezomib, the monomeric boronic acid, is [(1R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl-2[(pyrazinylcarbonyl) amino]propyl]amino]butyl] boronic acid.

Bortezomib has the following chemical structure:

VELCADE ® (bortezomib)  Structural Formula Illustration

The molecular weight is 384.24. The molecular formula is C19H25BN4O4. The solubility of bortezomib, as the monomeric boronic acid, in water is 3.3 to 3.8 mg/mL in a pH range of 2 to 6.5.

What are the possible side effects of bortezomib (Velcade)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have a serious side effect such as:

  • new or worsening nerve problems such as numbness, burning, pain, weakness, or tingly feeling;
  • feeling like you might pass out;
  • dry cough and trouble breathing;
  • severe headache, vision problems, confusion, and/or seizure (convulsions);
  • black, bloody, or tarry stools, vomit that looks like blood or coffee...

Read All Potential Side Effects and See Pictures of Velcade »

What are the precautions when taking bortezomib (Velcade)?

Before using this medication, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients (such as boron, mannitol), which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: nerve sensation problems (e.g., peripheral neuropathy), heart disease, low blood pressure, loss of body fluids (dehydration), diabetes, liver disease, severe kidney disease, certain viral infection (herpes, shingles).

To minimize dizziness and lightheadedness, get up slowly when rising from a seated or lying position.

This drug may make you dizzy or cause vision changes. Do not...

Read All Potential Precautions of Velcade »

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

INDICATIONS

Multiple Myeloma

VELCADE® (bortezomib) is indicated for the treatment of patients with multiple myeloma.

Mantle Cell Lymphoma

VELCADE is indicated for the treatment of patients with mantle cell lymphoma who have received at least 1 prior therapy.

DOSAGE AND ADMINISTRATION

General Dosing Guidelines

The recommended starting dose of VELCADE is 1.3 mg/m². VELCADE may be administered intravenously at a concentration of 1 mg/mL, or subcutaneously at a concentration of 2.5 mg/mL. When administered intravenously, VELCADE is administered as a 3 to 5 second bolus intravenous injection. VELCADE is for intravenous or subcutaneous use only. VELCADE should not be administered by any other route.

Because each route of administration has a different reconstituted concentration, caution should be used when calculating the volume to be administered.

Dosage in Previously Untreated Multiple Myeloma

VELCADE is administered in combination with oral melphalan and oral prednisone for nine 6-week treatment cycles as shown in Table 1. In Cycles 1-4, VELCADE is administered twice weekly (days 1, 4, 8, 11, 22, 25, 29 and 32). In Cycles 5-9, VELCADE is administered once weekly (days 1, 8, 22 and 29). At least 72 hours should elapse between consecutive doses of VELCADE.

Table 1: Dosage Regimen for Patients with Previously Untreated Multiple Myeloma

Twice Weekly VELCADE (Cycles 1-4) Week 1 2 3 4 5 6
VELCADE (1.3 mg/m²) Day 1 -- -- Day 4 Day 8 Day 11 rest period Day 22 Day 25 Day 29 Day 32 rest period
Melphalan(9 mg/m²) Prednisone(60 mg/m²) Day 1 Day 2 Day 3 Day 4 -- -- rest period -- -- -- -- rest period
Once Weekly VELCADE (Cycles 5-9 when used in combination with Melphalan and Prednisone)
Week 1 2 3 4 5 6
VELCADE (1.3 mg/m²) Day 1 -- -- Day 4 Day 8 Day 11 rest period Day 22 Day 25 Day 29 Day 32 rest period
Melphalan(9 mg/m²) Prednisone(60 mg/m²) Day 1 Day 2 Day 3 Day 4 -- -- rest period -- -- -- -- rest period

Dose Modification Guidelines for VELCADE When Given in Combination with Melphalan and Prednisone

Prior to initiating any cycle of therapy with VELCADE in combination with melphalan and prednisone:

Table 2: Dose Modifications during Cycles of Combination VELCADE, Melphalan and Prednisone Therapy

Toxicity Dose modification or delay
Hematological toxicity during a cycle: If prolonged Grade 4 neutropenia or thrombocytopenia, or thrombocytopenia with bleeding is observed in the previous cycle Consider reduction of the melphalan dose by 25% in the next cycle
If platelet count is not above 30 x 109/L or aNc is not above 0.75 x 109/L on a VELCADE dosing day (other than day 1) Withhold VELCADE dose
If several VELCADE doses in consecutive cycles are withheld due to toxicity Reduce VELCADE dose by 1 dose level (from 1.3 mg/m² to 1 mg/m², or from 1 mg/m² to 0.7 mg/m²)
Grade 3 or higher non-hematological toxicities Withhold VELCADE therapy until symptoms of toxicity have resolved to Grade 1 or baseline. Then, VELCADE may be reinitiated2 with one dose level reduction (from 1.3 mg/m² to 1 mg/m², or from 1 mg/m² to 0.7 mg/m²). For VELCADE-related neuropathic pain and/or peripheral neuropathy, hold or modify VELCADE as outlined in Table 3.

For information concerning melphalan and prednisone, see manufacturer's prescribing information.

Dose modifications guidelines for peripheral neuropathy are provided.

Dosage and Dose Modifications for Relapsed Multiple Myeloma and Mantle Cell Lymphoma

VELCADE (1.3 mg/m²/dose) is administered twice weekly for 2 weeks (Days 1, 4, 8, and 11) followed by a 10-day rest period (Days 12-21). For extended therapy of more than 8 cycles, VELCADE may be administered on the standard schedule or on a maintenance schedule of once weekly for 4 weeks (Days 1, 8, 15, and 22) followed by a 13-day rest period (Days 23 to 35) [see Clinical Studies]. At least 72 hours should elapse between consecutive doses of VELCADE.

VELCADE therapy should be withheld at the onset of any Grade 3 non-hematological or Grade 4 hematological toxicities excluding neuropathy as discussed below [see WARNINGS AND PRECAUTIONS]. Once the symptoms of the toxicity have resolved, VELCADE therapy may be reinitiated at a 25% reduced dose (1.3 mg/m²/dose reduced to 1 mg/m²/dose; 1 mg/m²/dose reduced to 0.7 mg/m²/dose).

For dose modifications guidelines for peripheral neuropathy see Management of Peripheral Neuropathy section.

Dose Modifications for Peripheral Neuropathy

Starting VELCADE subcutaneously may be considered for patients with pre-existing or at high risk of peripheral neuropathy. Patients with pre-existing severe neuropathy should be treated with VELCADE only after careful risk-benefit assessment.

Patients experiencing new or worsening peripheral neuropathy during VELCADE therapy may require a decrease in the dose and/or a less dose-intense schedule.

For dose or schedule modification guidelines for patients who experience VELCADE-related neuropathic pain and/or peripheral neuropathy see Table 3.

Table 3: Recommended Dose Modification for VELCADE related Neuropathic Pain and/or Peripheral Sensory or Motor Neuropathy

Severity of Peripheral Neuropathy Signs and Symptoms* Modification of Dose and Regimen
Grade 1 (asymptomatic; loss of deep tendon reflexes or paresthesia) without pain or loss of function No action
Grade 1 with pain or Grade 2 (moderate symptoms; limiting instrumental Activities of Daily Living (ADL)**) Reduce VELCADE to 1 mg/m²
Grade 2 with pain or Grade 3 (severe symptoms; limiting self care ADL ***) Withhold VELCADE therapy until toxicity resolves. When toxicity resolves reinitiate with a reduced dose of VELCADE at 0.7 mg/m² once per week.
Grade 4 (life-threatening consequences; urgent intervention indicated) Discontinue VELCADE
*Grading based on NCI Common Terminology Criteria CTCAE v4.0
**Instrumental ADL: refers to preparing meals, shopping for groceries or clothes, using telephone, managing money etc;
***Self care ADL: refers to bathing, dressing and undressing, feeding self, using the toilet, taking medications, and not bedridden

Dosage in Patients with Hepatic Impairment

Patients with mild hepatic impairment do not require a starting dose adjustment and should be treated per the recommended VELCADE dose. Patients with moderate or severe hepatic impairment should be started on VELCADE at a reduced dose of 0.7 mg/m²per injection during the first cycle, and a subsequent dose escalation to 1.0 mg/m²or further dose reduction to 0.5 mg/m²may be considered based on patient tolerance (see Table 4) [see Use In Specific Populations and CLINICAL PHARMACOLOGY].

Table 4: Recommended Starting Dose Modification for VELCADE in Patients with Hepatic Impairment

  Bilirubin Level SGOT (AST) Levels Modification of Starting Dose
Mild Less than or equal to 1.0x ULN More than ULN None
More than 1.0x-1.5x ULN Any None
Moderate More than 1.5x-3x ULN Any Reduce VELCADE to 0.7 mg/m² in the first cycle. Consider dose escalation to 1.0 mg/m² or further dose reduction to 0.5 mg/m² in subsequent cycles based on patient tolerability.
Severe More than 3x ULN Any
Abbreviations: SGOT = serum glutamic oxaloacetic transaminase;
AST = aspartate aminotransferase; ULN = upper limit of the normal range.

Administration Precautions

The drug quantity contained in one vial (3.5 mg) may exceed the usual dose required. Caution should be used in calculating the dose to prevent overdose.

When administered subcutaneously, sites for each injection (thigh or abdomen) should be rotated. New injections should be given at least one inch from an old site and never into areas where the site is tender, bruised, erythematous, or indurated.

If local injection site reactions occur following VELCADE administration subcutaneously, a less concentrated VELCADE solution (1 mg/mL instead of 2.5 mg/mL) may be administered subcutaneously. Alternatively, the intravenous route of administration should be considered.

VELCADE is an antineoplastic. Procedures for proper handling and disposal should be considered [see HOW SUPPLIED/Storage and Handling].

Reconstitution/Preparation for Intravenous and Subcutaneous Administration

Proper aseptic technique should be used. Reconstitute only with 0.9% sodium chloride. The reconstituted product should be a clear and colorless solution.

Different volumes of 0.9% sodium chloride are used to reconstitute the product for the different routes of administration. The reconstituted concentration of bortezomib for subcutaneous administration (2.5 mg/mL) is greater than the reconstituted concentration of bortezomib for intravenous administration (1 mg/mL). Because each route of administration has a different reconstituted concentration, caution should be used when calculating the volume to be administered.

For each 3.5 mg single-use vial of bortezomib reconstitute with the following volume of 0.9% sodium chloride based on route of administration (Table 5):

Table 5: Reconstitution Volumes and Final Concentration for Intravenous and Subcutaneous Administration

Route of administration Bortezomib (mg/vial) Diluent (0.9% Sodium Chloride) Final Bortezomib concentration (mg/mL)
Intravenous 3.5 mg 3.5 mL 1 mg/mL
Subcutaneous 3.5 mg 1.4 mL 2.5 mg/mL

Dose must be individualized to prevent overdosage. After determining patient body surface area (BSA) in square meters, use the following equations to calculate the total volume (mL) of reconstituted VELCADE to be administered:

  • Intravenous Administration [1 mg/mL concentration]

VELCADE dose (mg/m²) x patlent BSA (m²) / 1 mg / ml = Total VELCADE volume (ml) to be administered

  • Subcutaneous Administration [2.5 mg/mL concentration]

VELCADE dose (mg/m²) x patlent BSA (m²) / 2.5 mg / ml = Total VELCADE volume (ml) to be administered

Stickers that indicate the route of administration are provided with each VELCADE vial. These stickers should be placed directly on the syringe of VELCADE once VELCADE is prepared to help alert practitioners of the correct route of administration for VELCADE.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. If any discoloration or particulate matter is observed, the reconstituted product should not be used.

Stability: Unopened vials of VELCADE are stable until the date indicated on the package when stored in the original package protected from light.

VELCADE contains no antimicrobial preservative. Reconstituted VELCADE should be administered within 8 hours of preparation. When reconstituted as directed, VELCADE may be stored at 25°C (77°F). The reconstituted material may be stored in the original vial and/or the syringe prior to administration. The product may be stored for up to 8 hours in a syringe; however, total storage time for the reconstituted material must not exceed 8 hours when exposed to normal indoor lighting.

HOW SUPPLIED

Dosage Forms And Strengths

Each single-use vial of VELCADE contains 3.5 mg of bortezomib as a sterile lyophilized white to off-white powder.

Storage And Handling

VELCADE® (bortezomib) for Injection is supplied as individually cartoned 10 mL vials containing 3.5 mg of bortezomib as a white to off-white cake or powder.

NDC 63020-049-01

3.5 mg single use vial

Unopened vials may be stored at controlled room temperature 25°C (77°F); excursions permitted from 15 to 30°C (59 to 86°F) [see USP Controlled Room Temperature]. Retain in original package to protect from light.

Consider handling and disposal of VELCADE according to guidelines issued for cytotoxic drugs, including the use of gloves and other protective clothing to prevent skin contact1.

REFERENCES

1. “OSHA Hazardous Drugs“ (refer to antineoplastic weblinks including OSHA Technical Manual). OSHA. http://www.osha.gov/SLTC/hazardousdrugs/index.html

Distributed and Marketed by: Millennium Pharmaceuticals, Inc. 40 Landsdowne Street Cambridge, MA 02139. Rev 15

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

SIDE EFFECTS

The following adverse reactions are also discussed in other sections of the labeling:

Clinical Trials Safety Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

Summary of Clinical Trial in Patients with Previously Untreated Multiple Myeloma

Table 7 describes safety data from 340 patients with previously untreated multiple myeloma who received VELCADE (1.3 mg/m²) administered intravenously in combination with melphalan (9 mg/m²) and prednisone (60 mg/m²) in a prospective randomized study.

The safety profile of VELCADE in combination with melphalan/prednisone is consistent with the known safety profiles of both VELCADE and melphalan/prednisone.

Table 7: Most Commonly Reported Adverse Reactions ( ≥ 10% in the VELCADE, Melphalan and Prednisone arm) with Grades 3 and ≥ 4 Intensity in the Previously Untreated Multiple Myeloma Study

System Organ Class Preferred Term VELCADE, Melphalan and Prednisone
(n=340)
Melphalan and Prednisone
(n=337)
Total n (%) Toxicity 3 Grade, n (%) ≥ 4 Total n (%) Toxicity 3 Grade, n (%) ≥ 4
Blood and lymphatic system disorders
  Thrombocytopenia 164 (48) 60 (18) 57 (17) 140 (42) 48 (14) 39 (12)
  Neutropenia 160 (47) 101 (30) 33 (10) 143 (42) 77 (23) 42 (12)
  Anemia 109 (32) 41 (12) 4 (1) 156 (46) 61 (18) 18 (5)
  Leukopenia 108 (32) 64 (19) 8 (2) 93 (28) 53 (16) 11 (3)
  Lymphopenia 78 (23) 46 (14) 17 (5) 51 (15) 26 (8) 7 (2)
Gastrointestinal disorders
  Nausea 134 (39) 10 (3) 0 70 (21) 1 ( < 1) 0
  Diarrhea 119 (35) 19 (6) 2 (1) 20 (6) 1 ( < 1) 0
  Vomiting 87 (26) 13 (4) 0 41 (12) 2 (1) 0
  Constipation 77 (23) 2 (1) 0 14 (4) 0 0
  Abdominal Pain Upper 34 (10) 1 ( < 1) 0 20 (6) 0 0
Nervous system disorders
  Peripheral Neuropathya 156 (46) 42 (12) 2 (1) 4 (1) 0 0
  Neuralgia 117 (34) 27 (8) 2 (1) 1 ( < 1) 0 0
  Paresthesia 42 (12) 6 (2) 0 4 (1) 0 0
General disorders and administration site conditions
  Fatigue 85 (25) 19 (6) 2 (1) 48 (14) 4 (1) 0
  Asthenia 54 (16) 18 (5) 0 23 (7) 3 (1) 0
  Pyrexia 53 (16) 4 (1) 0 19 (6) 1 ( < 1) 1 ( < 1)
Infections and infestations
  Herpes Zoster 39 (11) 11 (3) 9 (3) 4 (1)
Metabolism and nutrition disorders
  Anorexia 64 (19) 6 (2) 19 (6) 0 0
Skin and subcutaneous tissue disorders
  Rash 38 (11) 2 (1) 7 (2) 0 0
Psychiatric disorders
  Insomnia 35 (10) 1 ( < 1) 21 (6) 0 0
aRepresents High Level Term Peripheral Neuropathies NEC

Relapsed Multiple Myeloma Randomized Study of VELCADE versus Dexamethasone

The safety data described below and in Table 8 reflect exposure to either VELCADE (n=331) or dexamethasone (n=332) in a study of patients with relapsed multiple myeloma. VELCADE was administered intravenously at doses of 1.3 mg/m²twice weekly for 2 out of 3 weeks (21-day cycle). After eight 21-day cycles patients continued therapy for three 35-day cycles on a weekly schedule. Duration of treatment was up to 11 cycles (9 months) with a median duration of 6 cycles (4.1 months). For inclusion in the trial, patients must have had measurable disease and 1 to 3 prior therapies. There was no upper age limit for entry. Creatinine clearance could be as low as 20 mL/min and bilirubin levels as high as 1.5 times the upper limit of normal. The overall frequency of adverse reactions was similar in men and women, and in patients < 65 and ≥ 65 years of age. Most patients were Caucasian [see Clinical Studies].

Among the 331 VELCADE-treated patients, the most commonly reported ( > 20%) adverse reactions overall were nausea (52%), diarrhea (52%), fatigue (39%), peripheral neuropathies NEC (35%), thrombocytopenia (33%), constipation (30%), vomiting (29%), and anorexia (21%). The most commonly reported ( > 20%) adverse reaction reported among the 332 patients in the dexamethasone group was fatigue (25%). Eight percent (8%) of patients in the VELCADE-treated arm experienced a Grade 4 adverse reaction; the most common reactions were thrombocytopenia (4%) and neutropenia (2%). Nine percent (9%) of dexamethasonetreated patients experienced a Grade 4 adverse reaction. All individual dexamethasone-related Grade 4 adverse reactions were less than 1%.

Serious Adverse Reactions and Adverse Reactions Leading to Treatment Discontinuation in the Relapsed Multiple Myeloma Study of VELCADE versus Dexamethasone

Serious adverse reactions are defined as any reaction that results in death, is life-threatening, requires hospitalization or prolongs a current hospitalization, results in a significant disability, or is deemed to be an important medical event. A total of 80 (24%) patients from the VELCADE treatment arm experienced a serious adverse reaction during the study, as did 83 (25%) dexamethasone-treated patients. The most commonly reported serious adverse reactions in the VELCADE treatment arm were diarrhea (3%), dehydration, herpes zoster, pyrexia, nausea, vomiting, dyspnea, and thrombocytopenia (2% each). In the dexamethasone treatment group, the most commonly reported serious adverse reactions were pneumonia (4%), hyperglycemia (3%), pyrexia, and psychotic disorder (2% each).

A total of 145 patients, including 84 (25%) of 331 patients in the VELCADE treatment group and 61 (18%) of 332 patients in the dexamethasone treatment group were discontinued from treatment due to adverse reactions. Among the 331 VELCADE treated patients, the most commonly reported adverse reaction leading to discontinuation was peripheral neuropathy (8%). Among the 332 patients in the dexamethasone group, the most commonly reported adverse reactions leading to treatment discontinuation were psychotic disorder and hyperglycemia (2% each).

Four deaths were considered to be VELCADE-related in this relapsed multiple myeloma study: 1 case each of cardiogenic shock, respiratory insufficiency, congestive heart failure and cardiac arrest. Four deaths were considered dexamethasone-related: 2 cases of sepsis, 1 case of bacterial meningitis, and 1 case of sudden death at home.

Most Commonly Reported Adverse Reactions in the Relapsed Multiple Myeloma Study of VELCADE versus Dexamethasone

The most common adverse reactions from the relapsed multiple myeloma study are shown in Table 8. All adverse reactions with incidence ≥ 10% in the VELCADE arm are included.

Table 8: Most Commonly Reported Adverse Reactions ( ≥ 10% in VELCADE arm), with Grades 3 and 4 Intensity in the Relapsed Multiple Myeloma Study of VELCADE versus Dexamethasone (N=663)

Preferred Term VELCADE
N=331
Dexamethasone
N=332
All Grade 3 Grade 4 All Grade 3 Grade 4
Adverse Reactions 324 (98) 193 (58) 28 (8) 297 (89) 110 (33) 29 (9)
Nausea 172 (52) 8 (2) 0 31 (9) 0 0
Diarrhea NOS 171 (52) 22 (7) 0 36 (11) 2 ( < 1) 0
Fatigue 130 (39) 15 (5) 0 82 (25) 8 (2) 0
Peripheral neuropathies NECa 115 (35) 23 (7) 2 ( < 1) 14 (4) 0 1 ( < 1)
Thrombocytopenia 109 (33) 80 (24) 12 (4) 11 (3) 5 (2) 1 ( < 1)
Constipation 99 (30) 6 (2) 0 27 (8) 1 ( < 1) 0
Vomiting NOS 96 (29) 8 (2) 0 10 (3) 1 ( < 1) 0
Anorexia 68 (21) 8 (2) 0 8 (2) 1 ( < 1) 0
Pyrexia 66 (20) 2 (< 1) 0 21 (6) 3 ( < 1) 1 ( < 1)
Paresthesia 64 (19) 5 (2) 0 24 (7) 0 0
Anemia NOS 63 (19) 20 (6) 1 ( < 1) 21 (6) 8 (2) 0
Headache NOS 62 (19) 3 ( < 1) 0 23 (7) 1 ( < 1) 0
Neutropenia 58 (18) 37 (11) 8 (2) 1 (< 1) 1 (< 1) 0
Rash NOS 43 (13) 3 ( < 1) 0 7 (2) 0 0
Appetite decreased NOS 36 (11) 0 0 12 (4) 0 0
Dyspnea NOS 35 (11) 11 (3) 1 ( < 1) 37 (11) 7 (2) 1 ( < 1)
Abdominal pain NOS 35 (11) 5 (2) 0 7 (2) 0 0
Weakness 34 (10) 10 (3) 0 28 (8) 8 (2) 0
aBased on High Level Term

Safety Experience from the Phase 2 Open-Label Extension Study in Relapsed Multiple Myeloma

In the phase 2 extension study of 63 patients, no new cumulative or new long-term toxicities were observed with prolonged VELCADE treatment. These patients were treated for a total of 5.3 to 23 months, including time on VELCADE in the prior VELCADE study [see Clinical Studies].

Safety Experience from the Phase 3 Open-Label Study of VELCADE Subcutaneous versus Intravenous in Relapsed Multiple Myeloma

The safety and efficacy of VELCADE administered subcutaneously were evaluated in one Phase 3 study at the recommended dose of 1.3 mg/m². This was a randomized, comparative study of VELCADE subcutaneous versus intravenous in 222 patients with relapsed multiple myeloma. The safety data described below and in Table 9 reflect exposure to either VELCADE subcutaneous (n=147) or VELCADE intravenous (n=74) [see Clinical Studies].

Table 9: Most Commonly Reported Adverse Reactions ( ≥ 10%), with Grade 3 and ≥ 4 Intensity in theRelapsed Multiple Myeloma Study (N=221) of VELCADE Subcutaneous versus Intravenous

System Organ Class Preferred Term Subcutaneous
(N=147)
Intravenous
(N=74)
Total n (%) Toxicity 3 Grade, n (%) ≥ 4 Total n (%) Toxicity 3 Grade, n (%) ≥ 4
Blood and lymphatic system disorders
  Anemia 28 (19) 8 (5) 0 17 (23) 3 (4) 0
  Leukopenia 26 (18) 8 (5) 0 15 (20) 4 (5) 1 (1)
  Neutropenia   34 (23) 15 (10) 4 (3) 20 (27) 10 (14) 3 (4)
  Thrombocytopenia 44 (30) 7 (5) 5 (3) 25 (34) 7 (9) 5 (7)
Gastrointestinal disorders
  Diarrhea 28 (19) 1 (1) 0 21 (28) 3 (4) 0
  Nausea 24 (16) 0 0 10 (14) 0 0
  Vomiting 13 (9) 3 (2) 0 8 (11) 0 0
General disorders and administration site conditions
  Asthenia 10 (7) 1 (1) 0 12 (16) 4 (5) 0
  Fatigue 11 (7) 3 (2) 0 11 (15) 3 (4) 0
  Pyrexia 18 (12) 0 0 6 (8) 0 0
Nervous system disorders
  Neuralgia 34 (23) 5 (3) 0 17 (23) 7 (9) 0
  Peripheral neuropathies NECa 55 (37) 8 (5) 1 (1) 37 (50) 10 (14) 1 (1)
Note: Safety population: 147 patients in the subcutaneous treatment group and 74 patients in the intravenous treatment group who received at least 1 dose of study medication
aRepresents MedDRA High Level Term.

In general, safety data were similar for the subcutaneous and intravenous treatment groups. Differences were observed in the rates of some Grade ≥ 3 adverse reactions. Differences of ≥ 5% were reported in neuralgia (3% subcutaneous versus 9% intravenous), peripheral neuropathies NEC (6% subcutaneous versus 15% intravenous), neutropenia (13% subcutaneous versus 18% intravenous), and thrombocytopenia (8% subcutaneous versus 16% intravenous).

A local reaction was reported in 6% of patients in the subcutaneous group, mostly redness. Only 2 (1%) patients were reported as having severe reactions, 1 case of pruritus and 1 case of redness. Local reactions led to reduction in injection concentration in one patient and drug discontinuation in one patient. Local reactions resolved in a median of 6 days.

Dose reductions occurred due to adverse reactions in 31% of patients in the subcutaneous treatment group compared with 43% of the intravenously-treated patients. The most common adverse reactions leading to a dose reduction included peripheral sensory neuropathy (17% in the subcutaneous treatment group compared with 31% in the intravenous treatment group); and neuralgia (11% in the subcutaneous treatment group compared with 19% in the intravenous treatment group).

Serious Adverse Reactions and Adverse Reactions Leading to Treatment Discontinuation in the Relapsed Multiple Myeloma Study of VELCADE Subcutaneous versus Intravenous

The incidence of serious adverse reactions was similar for the subcutaneous treatment group (20%) and the intravenous treatment group (19%). The most commonly reported serious adverse reactions in the subcutaneous treatment arm were pneumonia and pyrexia (2% each). In the intravenous treatment group, the most commonly reported serious adverse reactions were pneumonia, diarrhea, and peripheral sensory neuropathy (3% each).

In the subcutaneous treatment group, 27 patients (18%) discontinued study treatment due to an adverse reaction compared with 17 patients (23%) in the intravenous treatment group. Among the 147 subcutaneously-treated patients, the most commonly reported adverse reactions leading to discontinuation were peripheral sensory neuropathy (5%) and neuralgia (5%). Among the 74 patients in the intravenous treatment group, the most commonly reported adverse reactions leading to treatment discontinuation were peripheral sensory neuropathy (9%) and neuralgia (9%).

Two patients (1%) in the subcutaneous treatment group and 1 (1%) patient in the intravenous treatment group died due to an adverse reaction during treatment. In the subcutaneous group the causes of death were one case of pneumonia and one case of sudden death. In the intravenous group the cause of death was coronary artery insufficiency.

Integrated Summary of Safety (Relapsed Multiple Myeloma and Mantle Cell Lymphoma)

Safety data from phase 2 and 3 studies of single agent VELCADE 1.3 mg/m²/dose twice weekly for 2 weeks followed by a 10-day rest period in 1163 patients with previously-treated multiple myeloma (N=1008) and previously-treated mantle cell lymphoma (N=155) were integrated and tabulated. This analysis does not include data from the Phase 3 Open-Label Study of VELCADE subcutaneous versus intravenous in relapsed multiple myeloma. In the integrated studies, the safety profile of VELCADE was similar in patients with multiple myeloma and mantle cell lymphoma.

In the integrated analysis, the most commonly reported ( > 20%) adverse reactions were nausea (49%), diarrhea (46%), asthenic conditions including fatigue (41%) and weakness (11%), peripheral neuropathies NEC (38%), thrombocytopenia (32%), vomiting (28%), constipation (25%), and pyrexia (21%). Eleven percent (11%) of patients experienced at least 1 episode of ≥ Grade 4 toxicity, most commonly thrombocytopenia (4%) and neutropenia (2%).

In the Phase 2 relapsed multiple myeloma clinical trials of VELCADE administered intravenously, local skin irritation was reported in 5% of patients, but extravasation of VELCADE was not associated with tissue damage.

Serious Adverse Reactions and Adverse Reactions Leading to Treatment Discontinuation in the Integrated Summary of Safety

A total of 26% of patients experienced a serious adverse reaction during the studies. The most commonly reported serious adverse reactions included diarrhea, vomiting and pyrexia (3% each), nausea, dehydration, and thrombocytopenia (2% each) and pneumonia, dyspnea, peripheral neuropathies NEC, and herpes zoster (1% each).

Adverse reactions leading to discontinuation occurred in 22% of patients. The reasons for discontinuation included peripheral neuropathy (8%), and fatigue, thrombocytopenia, and diarrhea (2% each).

In total, 2% of the patients died and the cause of death was considered by the investigator to be possibly related to study drug: including reports of cardiac arrest, congestive heart failure, respiratory failure, renal failure, pneumonia and sepsis.

Most Commonly Reported Adverse Reactions in the Integrated Summary of Safety

The most common adverse reactions are shown in Table 10. All adverse reactions occurring at ≥ 10% are included. In the absence of a randomized comparator arm, it is often not possible to distinguish between adverse events that are drug-caused and those that reflect the patient's underlying disease. Please see the discussion of specific adverse reactions that follows.

Table 10: Most Commonly Reported ( ≥ 10% Overall) Adverse Reactionsin Integrated Analyses of Relapsed Multiple Myeloma and Mantle Cell Lymphoma Studies using the 1.3 mg/m² Dose (N=1163)

Preferred Term All Patients
N=1163
Multiple Myeloma
N=1008
Mantle Cell Lymphoma
N=155
All ≥ Grade 3 All ≥ Grade 3 All ≥ Grade 3
Nausea 567 (49) 36 (3) 511 (51) 32 (3) 56 (36) 4 (3)
Diarrhea NOS 530 (46) 83 (7) 470 (47) 72 (7) 60 (39) 11 (7)
Fatigue 477 (41) 86 (7) 396 (39) 71 (7) 81 (52) 15 (10)
Peripheral neuropathies NECa 443 (38) 129 (11) 359 (36) 110 (11) 84 (54) 19 (12)
Thrombocytopenia 369 (32) 295 (25) 344 (34) 283 (28) 25 (16) 12 (8)
Vomiting NOS 321 (28) 44 (4) 286 (28) 40 (4) 35 (23) 4 (3)
Constipation 296 (25) 17 (1) 244 (24) 14 (1) 52 (34) 3 (2)
Pyrexia 249 (21) 16 (1) 233 (23) 15 (1) 16 (10) 1 ( < 1)
Anorexia 227 (20) 19 (2) 205 (20) 16 (2) 22 (14) 3 (2)
Anemia NOS 209 (18) 65 (6) 190 (19) 63 (6) 19 (12) 2 (1)
Headache NOS 175 (15) 8 ( < 1) 160 (16) 8 ( < 1) 15 (10) 0
Neutropenia 172 (15) 121 (10) 164 (16) 117 (12) 8 (5) 4 (3)
Rash NOS 156 (13) 8 ( < 1) 120 (12) 4 ( < 1) 36 (23) 4 (3)
Paresthesia 147 (13) 9 ( < 1) 136 (13) 8 ( < 1) 11 (7) 1 ( < 1)
Dizziness (excl vertigo) 129 (11) 13 (1) 101 (10) 9 ( < 1) 28 (18) 4 (3)
Weakness 124 (11) 31 (3) 106 (11) 28 (3) 18 (12) 3 (2)
a Based on High Level Term

Description of Selected Adverse Reactions from the Integrated Phase 2 and 3 Relapsed Multiple Myeloma and Phase 2 Mantle Cell Lymphoma Studies
Gastrointestinal Toxicity

A total of 75% of patients experienced at least one gastrointestinal disorder. The most common gastrointestinal disorders included nausea, diarrhea, constipation, vomiting, and appetite decreased. Other gastrointestinal disorders included dyspepsia and dysgeusia. Grade 3 adverse reactions occurred in 14% of patients; ≥ Grade 4 adverse reactions were ≤ 1%. Gastrointestinal adverse reactions were considered serious in 7% of patients. Four percent (4%) of patients discontinued due to a gastrointestinal adverse reaction. Nausea was reported more often in patients with multiple myeloma (51%) compared to patients with mantle cell lymphoma (36%).

Thrombocytopenia

Across the studies, VELCADE-associated thrombocytopenia was characterized by a decrease in platelet count during the dosing period (days 1 to 11) and a return toward baseline during the 10-day rest period during each treatment cycle. Overall, thrombocytopenia was reported in 32% of patients. Thrombocytopenia was Grade 3 in 22%, ≥ Grade 4 in 4%, and serious in 2% of patients, and the reaction resulted in VELCADE discontinuation in 2% of patients. Thrombocytopenia was reported more often in patients with multiple myeloma (34%) compared to patients with mantle cell lymphoma (16%). The incidence of ≥ Grade 3 thrombocytopenia also was higher in patients with multiple myeloma (28%) compared to patients with mantle cell lymphoma (8%).

Peripheral Neuropathy

Overall, peripheral neuropathies NEC occurred in 38% of patients. Peripheral neuropathy was Grade 3 for 11% of patients and ≥ Grade 4 for < 1% of patients. Eight percent (8%) of patients discontinued VELCADE due to peripheral neuropathy. The incidence of peripheral neuropathy was higher among patients with mantle cell lymphoma (54%) compared to patients with multiple myeloma (36%).

In the VELCADE versus dexamethasone phase 3 relapsed multiple myeloma study, among the 62 VELCADE-treated patients who experienced ≥ Grade 2 peripheral neuropathy and had dose adjustments, 48% had improved or resolved with a median of 3.8 months from first onset.

In the phase 2 relapsed multiple myeloma studies, among the 30 patients who experienced Grade 2 peripheral neuropathy resulting in discontinuation or who experienced ≥ Grade 3 peripheral neuropathy, 73% reported improvement or resolution with a median time of 47 days to improvement of one Grade or more from the last dose of VELCADE.

Hypotension

The incidence of hypotension (postural, orthostatic and hypotension NOS) was 8% in patients treated with VELCADE. Hypotension was Grade 1 or 2 in the majority of patients and Grade 3 in 2% and ≥ Grade 4 in < 1%. Two percent (2%) of patients had hypotension reported as a serious adverse reaction, and 1% discontinued due to hypotension. The incidence of hypotension was similar in patients with multiple myeloma (8%) and those with mantle cell lymphoma (9%). In addition, < 1% of patients experienced hypotension associated with a syncopal reaction.

Neutropenia

Neutrophil counts decreased during the VELCADE dosing period (days 1 to 11) and returned toward baseline during the 10-day rest period during each treatment cycle. Overall, neutropenia occurred in 15% of patients and was Grade 3 in 8% of patients and ≥ Grade 4 in 2%. Neutropenia was reported as a serious adverse reaction in < 1% of patients and < 1% of patients discontinued due to neutropenia. The incidence of neutropenia was higher in patients with multiple myeloma (16%) compared to patients with mantle cell lymphoma (5%). The incidence of ≥ Grade 3 neutropenia also was higher in patients with multiple myeloma (12%) compared to patients with mantle cell lymphoma (3%).

Asthenic conditions (Fatigue, Malaise, Weakness, Asthenia)

Asthenic conditions were reported in 54% of patients. Fatigue was reported as Grade 3 in 7% and ≥ Grade 4 in < 1% of patients. Asthenia was reported as Grade 3 in 2% and ≥ Grade 4 in < 1% of patients. Two percent (2%) of patients discontinued treatment due to fatigue and < 1% due to weakness and asthenia. Asthenic conditions were reported in 53% of patients with multiple myeloma and 59% of patients with mantle cell lymphoma.

Pyrexia

Pyrexia ( > 38°C) was reported as an adverse reaction for 21% of patients. The reaction was Grade 3 in 1% and ≥ Grade 4 in < 1%. Pyrexia was reported as a serious adverse reaction in 3% of patients and led to VELCADE discontinuation in < 1% of patients. The incidence of pyrexia was higher among patients with multiple myeloma (23%) compared to patients with mantle cell lymphoma (10%). The incidence of ≥ Grade 3 pyrexia was 1% in patients with multiple myeloma and < 1% in patients with mantle cell lymphoma.

Herpes Virus Infection

Consider using antiviral prophylaxis in subjects being treated with VELCADE. In the randomized studies in previously untreated and relapsed multiple myeloma, herpes zoster reactivation was more common in subjects treated with VELCADE (ranging between 6-11%) than in the control groups (3-4%). Herpes simplex was seen in 1-3% in subjects treated with VELCADE and 1-3% in the control groups. In the previously untreated multiple myeloma study, herpes zoster virus reactivation in the VELCADE, melphalan and prednisone arm was less common in subjects receiving prophylactic antiviral therapy (3%) than in subjects who did not receive prophylactic antiviral therapy (17%).

Additional Adverse Reactions from Clinical Studies

The following clinically important serious adverse reactions that are not described above have been reported in clinical trials in patients treated with VELCADE administered as monotherapy or in combination with other chemotherapeutics. These studies were conducted in patients with hematological malignancies and in solid tumors.

Blood and lymphatic system disorders: Anemia, disseminated intravascular coagulation, febrile neutropenia, lymphopenia, leukopenia

Cardiac disorders: Angina pectoris, atrial fibrillation aggravated, atrial flutter, bradycardia, sinus arrest, cardiac amyloidosis, complete atrioventricular block, myocardial ischemia, myocardial infarction, pericarditis, pericardial effusion, Torsades de pointes, ventricular tachycardia

Ear and labyrinth disorders: Hearing impaired, vertigo

Eye disorders: Diplopia and blurred vision, conjunctival infection, irritation

Gastrointestinal disorders: Abdominal pain, ascites, dysphagia, fecal impaction, gastroenteritis, gastritis hemorrhagic, hematemesis, hemorrhagic duodenitis, ileus paralytic, large intestinal obstruction, paralytic intestinal obstruction, peritonitis, small intestinal obstruction, large intestinal perforation, stomatitis, melena, pancreatitis acute, oral mucosal petechiae, gastroesophageal reflux

General disorders and administration site conditions: Chills, edema, edema peripheral, injection site erythema, neuralgia, injection site pain, irritation, malaise, phlebitis

Hepatobiliary disorders: Cholestasis, hepatic hemorrhage, hyperbilirubinemia, portal vein thrombosis, hepatitis, liver failure

Immune system disorders: Anaphylactic reaction, drug hypersensitivity, immune complex mediated hypersensitivity, angioedema, laryngeal edema

Infections and infestations: Aspergillosis, bacteremia, bronchitis, urinary tract infection, herpes viral infection, listeriosis, nasopharyngitis, pneumonia, respiratory tract infection, septic shock, toxoplasmosis, oral candidiasis, sinusitis, catheter related infection

Injury, poisoning and procedural complications: Catheter related complication, skeletal fracture, subdural hematoma

Investigations: Weight decreased

Metabolism and nutrition disorders: Dehydration, hypocalcemia, hyperuricemia, hypokalemia, hyperkalemia, hyponatremia, hypernatremia

Musculoskeletal and connective tissue disorders: Arthralgia, back pain, bone pain, myalgia, pain in extremity

Nervous system disorders: Ataxia, coma, dizziness, dysarthria, dysesthesia, dysautonomia, encephalopathy, cranial palsy, grand mal convulsion, headache, hemorrhagic stroke, motor dysfunction, neuralgia, spinal cord compression, paralysis, postherpetic neuralgia, transient ischemic attack

Psychiatric disorders: Agitation, anxiety, confusion, insomnia, mental status change, psychotic disorder, suicidal ideation

Renal and urinary disorders: Calculus renal, bilateral hydronephrosis, bladder spasm, hematuria, hemorrhagic cystitis, urinary incontinence, urinary retention, renal failure (acute and chronic), glomerular nephritis proliferative

Respiratory, thoracic and mediastinal disorders: Acute respiratory distress syndrome, aspiration pneumonia, atelectasis, chronic obstructive airways disease exacerbated, cough, dysphagia, dyspnea, dyspnea exertional, epistaxis, hemoptysis, hypoxia, lung infiltration, pleural effusion, pneumonitis, respiratory distress, pulmonary hypertension

Skin and subcutaneous tissue disorders: Urticaria, face edema, rash (which may be pruritic), leukocytoclastic vasculitis, pruritus.

Vascular disorders: Cerebrovascular accident, cerebral hemorrhage, deep venous thrombosis, hypertension, peripheral embolism, pulmonary embolism, pulmonary hypertension

Postmarketing Experience

The following adverse reactions have been identified from the worldwide postmarketing experience with VELCADE. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure: atrioventricular block complete, cardiac tamponade, ischemic colitis, encephalopathy, dysautonomia, deafness bilateral, disseminated intravascular coagulation, hepatitis, acute pancreatitis, progressive multifocal leukoencephalopathy (PML), acute diffuse infiltrative pulmonary disease, PRES (formerly RPLS), toxic epidermal necrolysis, acute febrile neutrophilic dermatosis (Sweet's syndrome), herpes meningoencephalitis, optic neuropathy, blindness and ophthalmic herpes.

Read the Velcade (bortezomib) Side Effects Center for a complete guide to possible side effects »

DRUG INTERACTIONS

Bortezomib is a substrate of cytochrome P450 enzyme 3A4, 2C19 and 1A2.

CYP3A4 inhibitors

Co-administration of ketoconazole, a strong CYP3A4 inhibitor, increased the exposure of bortezomib by 35% in 12 patients. Monitor patients for signs of bortezomib toxicity and consider a bortezomib dose reduction if bortezomib must be given in combination with strong CYP3A4 inhibitors (e.g. ketoconazole, ritonavir).

CYP2C19 inhibitors

Co-administration of omeprazole, a strong inhibitor of CYP2C19, had no effect on the exposure of bortezomib in 17 patients.

CYP3A4 inducers

Co-administration of rifampin, a strong CYP3A4 inducer, is expected to decrease the exposure of bortezomib by at least 45%. Because the drug interaction study (n=6) was not designed to exert the maximum effect of rifampin on bortezomib PK, decreases greater than 45% may occur.

Efficacy may be reduced when VELCADE is used in combination with strong CYP3A4 inducers; therefore, concomitant use of strong CYP3A4 inducers is not recommended in patients receiving VELCADE.

St. John's Wort (Hypericum perforatum) may decrease bortezomib exposure unpredictably and should be avoided.

Dexamethasone

Co-administration of dexamethasone, a weak CYP3A4 inducer, had no effect on the exposure of bortezomib in 7 patients.

Melphalan-Prednisone

Co-administration of melphalan-prednisone increased the exposure of bortezomib by 17% in 21 patients. However, this increase is unlikely to be clinically relevant.

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

WARNINGS

Included as part of the PRECAUTIONS section.

PRECAUTIONS

Peripheral Neuropathy

VELCADE treatment causes a peripheral neuropathy that is predominantly sensory; however, cases of severe sensory and motor peripheral neuropathy have been reported. Patients with pre-existing symptoms (numbness, pain or a burning feeling in the feet or hands) and/or signs of peripheral neuropathy may experience worsening peripheral neuropathy (including ≥ Grade 3) during treatment with VELCADE. Patients should be monitored for symptoms of neuropathy, such as a burning sensation, hyperesthesia, hypoesthesia, paresthesia, discomfort, neuropathic pain or weakness. In the Phase 3 relapsed multiple myeloma trial comparing VELCADE subcutaneous versus intravenous the incidence of Grade ≥ 2 peripheral neuropathy was 24% for subcutaneous and 39% for intravenous. Grade ≥ 3 peripheral neuropathy occurred in 6% of patients in the subcutaneous treatment group, compared with 15% in the intravenous treatment group. Starting VELCADE subcutaneously may be considered for patients with pre-existing or at high risk of peripheral neuropathy.

Patients experiencing new or worsening peripheral neuropathy during VELCADE therapy may require a decrease in the dose and/or a less dose-intense schedule [see DOSAGE AND ADMINISTRATION]. In the VELCADE versus dexamethasone phase 3 relapsed multiple myeloma study, improvement in or resolution of peripheral neuropathy was reported in 48% of patients with ≥ Grade 2 peripheral neuropathy following dose adjustment or interruption. Improvement in or resolution of peripheral neuropathy was reported in 73% of patients who discontinued due to Grade 2 neuropathy or who had ≥ Grade 3 peripheral neuropathy in the phase 2 multiple myeloma studies [see ADVERSE REACTIONS]. The long-term outcome of peripheral neuropathy has not been studied in mantle cell lymphoma.

Hypotension

The incidence of hypotension (postural, orthostatic, and hypotension NOS) was 8%. These events are observed throughout therapy. Caution should be used when treating patients with a history of syncope, patients receiving medications known to be associated with hypotension, and patients who are dehydrated. Management of orthostatic/postural hypotension may include adjustment of antihypertensive medications, hydration, and administration of mineralocorticoids and/or sympathomimetics [see ADVERSE REACTIONS].

Cardiac Toxicity

Acute development or exacerbation of congestive heart failure and new onset of decreased left ventricular ejection fraction have occurred during VELCADE therapy, including reports in patients with no risk factors for decreased left ventricular ejection fraction. Patients with risk factors for, or existing heart disease should be closely monitored. In the relapsed multiple myeloma study of VELCADE versus dexamethasone, the incidence of any treatment-related cardiac disorder was 8% and 5% in the VELCADE and dexamethasone groups, respectively. The incidence of adverse reactions suggestive of heart failure (acute pulmonary edema, pulmonary edema, cardiac failure, congestive cardiac failure, cardiogenic shock) was ≤ 1% for each individual reaction in the VELCADE group. In the dexamethasone group the incidence was ≤ 1% for cardiac failure and congestive cardiac failure; there were no reported reactions of acute pulmonary edema, pulmonary edema, or cardiogenic shock. There have been isolated cases of QT-interval prolongation in clinical studies; causality has not been established.

Pulmonary Toxicity

Acute Respiratory Distress Syndrome (ARDS) and acute diffuse infiltrative pulmonary disease of unknown etiology such as pneumonitis, interstitial pneumonia, lung infiltration have occurred in patients receiving VELCADE. Some of these events have been fatal.

In a clinical trial, the first two patients given high-dose cytarabine (2g/m²per day) by continuous infusion with daunorubicin and VELCADE for relapsed acute myelogenous leukemia died of ARDS early in the course of therapy.

There have been reports of pulmonary hypertension associated with VELCADE administration in the absence of left heart failure or significant pulmonary disease.

In the event of new or worsening cardiopulmonary symptoms, consider interrupting VELCADE until a prompt and comprehensive diagnostic evaluation is conducted.

Posterior Reversible Encephalopathy Syndrome (PRES)

Posterior Reversible Encephalopathy Syndrome (PRES; formerly termed Reversible Posterior Leukoencephalopathy Syndrome (RPLS)) has occurred in patients receiving VELCADE. PRES is a rare, reversible, neurological disorder which can present with seizure, hypertension, headache, lethargy, confusion, blindness, and other visual and neurological disturbances. Brain imaging, preferably MRI (Magnetic Resonance Imaging), is used to confirm the diagnosis. In patients developing PRES, discontinue VELCADE. The safety of reinitiating VELCADE therapy in patients previously experiencing PRES is not known.

Gastrointestinal Toxicity

VELCADE treatment can cause nausea, diarrhea, constipation, and vomiting [see ADVERSE REACTIONS] sometimes requiring use of antiemetic and antidiarrheal medications. Ileus can occur. Fluid and electrolyte replacement should be administered to prevent dehydration. Interrupt VELCADE for severe symptoms.

Thrombocytopenia/Neutropenia

VELCADE is associated with thrombocytopenia and neutropenia that follow a cyclical pattern with nadirs occurring following the last dose of each cycle and typically recovering prior to initiation of the subsequent cycle. The cyclical pattern of platelet and neutrophil decreases and recovery remained consistent over the 8 cycles of twice weekly dosing, and there was no evidence of cumulative thrombocytopenia or neutropenia. The mean platelet count nadir measured was approximately 40% of baseline. The severity of thrombocytopenia related to pretreatment platelet count is shown in Table 6. In the relapsed multiple myeloma study of VELCADE versus dexamethasone, the incidence of bleeding ( ≥ Grade 3) was 2% on the VELCADE arm and was < 1% in the dexamethasone arm. Complete blood counts (CBC) should be monitored frequently during treatment with VELCADE. Platelet count should be monitored prior to each dose of VELCADE. Patients experiencing thrombocytopenia may require change in the dose and schedule of VELCADE [see Table 2 and DOSAGE AND ADMINISTRATION]. Gastrointestinal and intracerebral hemorrhage has been reported in association with VELCADE. Transfusions may be considered.

Table 6: Severity of Thrombocytopenia Related to Pretreatment Platelet Count in the Relapsed Multiple Myeloma Study of VELCADE versus Dexamethasone

Number (%) of Number of Pretreatment Platelet Count* Patients
(N=331)**
Patients with Platelet Count < 10,000/μL Number (%) of Patients with Platelet Count 10,000-25,000/μL
≥ 75,000/μL 309 8 (3%) 36 (12%)
≥ 50,000/μL- < 75,000/μL 14 2 (14%) 11 (79%)
≥ 10,000/μL- < 50,000/μL 7 1 (14%) 5 (71%)
* A baseline platelet count of 50,000/μL was required for study eligibility
** Data were missing at baseline for 1 patient

Tumor Lysis Syndrome

Tumor lysis syndrome has been reported with VELCADE therapy. Patients at risk of tumor lysis syndrome are those with high tumor burden prior to treatment. Monitor patients closely and take appropriate precautions.

Hepatic Toxicity

Cases of acute liver failure have been reported in patients receiving multiple concomitant medications and with serious underlying medical conditions. Other reported hepatic reactions include hepatitis, increases in liver enzymes, and hyperbilirubinemia. Interrupt VELCADE therapy to assess reversibility. There is limited re-challenge information in these patients.

Embryo-fetal Risk

Women of reproductive potential should avoid becoming pregnant while being treated with VELCADE. Bortezomib administered to rabbits during organogenesis at a dose approximately 0.5 times the clinical dose of 1.3 mg/m²based on body surface area caused post-implantation loss and a decreased number of live fetuses [see Use in Specific Populations].

Nonclinical Toxicology

Carcinogenesis, Mutagenesis, Impairment of Fertility

Carcinogenicity studies have not been conducted with bortezomib.

Bortezomib showed clastogenic activity (structural chromosomal aberrations) in the in vitro chromosomal aberration assay using Chinese hamster ovary cells. Bortezomib was not genotoxic when tested in the in vitro mutagenicity assay (Ames test) and in vivo micronucleus assay in mice.

Fertility studies with bortezomib were not performed but evaluation of reproductive tissues has been performed in the general toxicity studies. In the 6-month rat toxicity study, degenerative effects in the ovary were observed at doses ≥ 0.3 mg/m²(one-fourth of the recommended clinical dose), and degenerative changes in the testes occurred at 1.2 mg/m². VELCADE could have a potential effect on either male or female fertility.

Use In Specific Populations

Pregnancy

Pregnancy Category D [see WARNINGS AND PRECAUTIONS].

Bortezomib was not teratogenic in nonclinical developmental toxicity studies in rats and rabbits at the highest dose tested (0.075 mg/kg; 0.5 mg/m²in the rat and 0.05 mg/kg; 0.6 mg/m²in the rabbit) when administered during organogenesis. These dosages are approximately half the clinical dose of 1.3 mg/m²based on body surface area.

Pregnant rabbits given bortezomib during organogenesis at a dose of 0.05mg/kg (0.6 mg/m²) experienced significant post-implantation loss and decreased number of live fetuses. Live fetuses from these litters also showed significant decreases in fetal weight. The dose is approximately 0.5 times the clinical dose of 1.3 mg/m²based on body surface area.

There are no adequate and well-controlled studies in pregnant women. If VELCADE is used during pregnancy, or if the patient becomes pregnant while receiving this drug, the patient should be apprised of the potential hazard to the fetus.

Nursing Mothers

It is not known whether bortezomib is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from VELCADE, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use

The safety and effectiveness of VELCADE in children have not been established.

Geriatric Use

Of the 669 patients enrolled in the relapsed multiple myeloma study, 245 (37%) were 65 years of age or older: 125 (38%) on the VELCADE arm and 120 (36%) on the dexamethasone arm. Median time to progression and median duration of response for patients ≥ 65 were longer on VELCADE compared to dexamethasone [5.5 mo versus 4.3 mo, and 8.0 mo versus 4.9 mo, respectively]. On the VELCADE arm, 40% (n=46) of evaluable patients aged ≥ 65 experienced response (CR+PR) versus 18% (n=21) on the dexamethasone arm. The incidence of Grade 3 and 4 events was 64%, 78% and 75% for VELCADE patients ≤ 50, 51-64 and ≥ 65 years old, respectively [see ADVERSE REACTIONS; Clinical Studies].

No overall differences in safety or effectiveness were observed between patients ≥ age 65 and younger patients receiving VELCADE; but greater sensitivity of some older individuals cannot be ruled out.

Patients with Renal Impairment

The pharmacokinetics of VELCADE are not influenced by the degree of renal impairment. Therefore, dosing adjustments of VELCADE are not necessary for patients with renal insufficiency. Since dialysis may reduce VELCADE concentrations, VELCADE should be administered after the dialysis procedure [see CLINICAL PHARMACOLOGY].

Patients with Hepatic Impairment

The exposure of bortezomib is increased in patients with moderate (bilirubin ≥ 1.5 – 3x ULN) and severe (bilirubin > 3 x ULN) hepatic impairment. Starting dose should be reduced in those patients [see DOSAGE AND ADMINISTRATION, CLINICAL PHARMACOLOGY].

Patients with Diabetes

During clinical trials, hypoglycemia and hyperglycemia were reported in diabetic patients receiving oral hypoglycemics. Patients on oral anti-diabetic agents receiving VELCADE treatment may require close monitoring of their blood glucose levels and adjustment of the dose of their anti-diabetic medication.

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

OVERDOSE

There is no known specific antidote for VELCADE overdosage. In humans, fatal outcomes following the administration of more than twice the recommended therapeutic dose have been reported, which were associated with the acute onset of symptomatic hypotension (5.2) and thrombocytopenia (5.7). In the event of an overdosage, the patient's vital signs should be monitored and appropriate supportive care given.

Studies in monkeys and dogs showed that intravenous bortezomib doses as low as 2 times the recommended clinical dose on a mg/m²basis were associated with increases in heart rate, decreases in contractility, hypotension, and death. In dog studies, a slight increase in the corrected QT interval was observed at doses resulting in death. In monkeys, doses of 3.0 mg/m²and greater (approximately twice the recommended clinical dose) resulted in hypotension starting at 1 hour post-administration, with progression to death in 12 to 14 hours following drug administration.

CONTRAINDICATIONS

VELCADE is contraindicated in patients with hypersensitivity (not including local reactions) to bortezomib, boron, or mannitol. Reactions have included anaphylactic reactions [see ADVERSE REACTIONS].

VELCADE is contraindicated for intrathecal administration. Fatal events have occurred with intrathecal administration of VELCADE.

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

CLINICAL PHARMACOLOGY

Mechanism of Action

Bortezomib is a reversible inhibitor of the chymotrypsin-like activity of the 26S proteasome in mammalian cells. The 26S proteasome is a large protein complex that degrades ubiquitinated proteins. The ubiquitinproteasome pathway plays an essential role in regulating the intracellular concentration of specific proteins, thereby maintaining homeostasis within cells. Inhibition of the 26S proteasome prevents this targeted proteolysis, which can affect multiple signaling cascades within the cell. This disruption of normal homeostatic mechanisms can lead to cell death. Experiments have demonstrated that bortezomib is cytotoxic to a variety of cancer cell types in vitro . Bortezomib causes a delay in tumor growth in vivo in nonclinical tumor models, including multiple myeloma.

Pharmacodynamics

Following twice weekly administration of 1 mg/m²and 1.3 mg/m²bortezomib doses (n=12 per each dose level), the maximum inhibition of 20S proteasome activity (relative to baseline) in whole blood was observed 5 minutes after drug administration. Comparable maximum inhibition of 20S proteasome activity was observed between 1 and 1.3 mg/m²doses. Maximal inhibition ranged from 70% to 84% and from 73% to 83% for the 1 mg/m²and 1.3 mg/m²dose regimens, respectively.

Pharmacokinetics

Following intravenous administration of 1 mg/m²and 1.3 mg/m²doses to 24 patients with multiple myeloma (n=12, per each dose level), the mean maximum plasma concentrations of bortezomib (Cmax) after the first dose (Day 1) were 57 and 112 ng/mL, respectively. In subsequent doses, when administered twice weekly, the mean maximum observed plasma concentrations ranged from 67 to 106 ng/mL for the 1 mg/m²dose and 89 to 120 ng/mL for the 1.3 mg/m²dose. The mean elimination half-life of bortezomib upon multiple dosing ranged from 40 to 193 hours after the 1 mg/m²dose and 76 to 108 hours after the 1.3mg/m²dose. The mean total body clearances was 102 and 112 L/h following the first dose for doses of 1 mg/m²and 1.3 mg/m², respectively, and ranged from 15 to 32 L/h following subsequent doses for doses of 1 and 1.3 mg/m², respectively.

Following an intravenous bolus or subcutaneous injection of a 1.3 mg/m²dose to patients (n = 14 for intravenous, n = 17 for subcutaneous) with multiple myeloma, the total systemic exposure after repeat dose administration (AUClast) was equivalent for subcutaneous and intravenous administration. The Cmax after subcutaneous administration (20.4 ng/mL) was lower than intravenous (223 ng/mL). The AUClast geometric mean ratio was 0.99 and 90% confidence intervals were 80.18% - 122.80%.

Distribution

The mean distribution volume of bortezomib ranged from approximately 498 to 1884 L/m²following single- or repeat-dose administration of 1 mg/m²or 1.3mg/m²to patients with multiple myeloma. This suggests bortezomib distributes widely to peripheral tissues. The binding of bortezomib to human plasma proteins averaged 83% over the concentration range of 100 to 1000 ng/mL.

Metabolism

In vitro studies with human liver microsomes and human cDNA-expressed cytochrome P450 isozymes indicate that bortezomib is primarily oxidatively metabolized via cytochrome P450 enzymes 3A4, 2C19, and 1A2. Bortezomib metabolism by CYP 2D6 and 2C9 enzymes is minor. The major metabolic pathway is deboronation to form 2 deboronated metabolites that subsequently undergo hydroxylation to several metabolites. Deboronated bortezomib metabolites are inactive as 26S proteasome inhibitors. Pooled plasma data from 8 patients at 10 min and 30 min after dosing indicate that the plasma levels of metabolites are low compared to the parent drug.

Elimination

The pathways of elimination of bortezomib have not been characterized in humans.

Age

Analyses of data after the first dose of Cycle 1 (Day 1) in 39 multiple myeloma patients who had received intravenous doses of 1 mg/m²and 1.3 mg/m²showed that both dose-normalized AUC and Cmax tend to be less in younger patients. Patients < 65 years of age (n=26) had about 25% lower mean dose-normalized AUC and Cmax than those ≥ 65 years of age (n=13).

Gender

Mean dose-normalized AUC and Cmax values were comparable between male (n=22) and female (n=17) patients after the first dose of Cycle 1 for the 1 and 1.3 mg/m²doses.

Race

The effect of race on exposure to bortezomib could not be assessed as most of the patients were Caucasian.

Hepatic Impairment

The effect of hepatic impairment (see Table 4 for definition of hepatic impairment) on the pharmacokinetics of bortezomib was assessed in 60 patients with cancer at bortezomib doses ranging from 0.5 to 1.3 mg/m². When compared to patients with normal hepatic function, mild hepatic impairment did not alter dose-normalized bortezomib AUC. However, the dose-normalized mean AUC values were increased by approximately 60% in patients with moderate or severe hepatic impairment. A lower starting dose is recommended in patients with moderate or severe hepatic impairment, and those patients should be monitored closely [see DOSAGE AND ADMINISTRATION and Use in Specific Populations].

Renal Impairment

A pharmacokinetic study was conducted in patients with various degrees of renal impairment who were classified according to their creatinine clearance values (CrCl) into the following groups: Normal (CrCl ≥ 60 mL/min/1.73 m², N=12), Mild (CrCl=40-59 mL/min/1.73 m², N=10), Moderate (CrCl=20-39 mL/min/1.73 m², N=9), and Severe (CrCl < 20 mL/min/1.73 m², N=3). A group of dialysis patients who were dosed after dialysis was also included in the study (N=8). Patients were administered intravenous doses of 0.7 to 1.3 mg/m²of bortezomib twice weekly. Exposure of bortezomib (dose-normalized AUC and Cmax) was comparable among all the groups [see Use in Specific Populations].

Pediatric

There are no pharmacokinetic data in pediatric patients.

Cytochrome P450

Bortezomib is a poor inhibitor of human liver microsome cytochrome P450 1A2, 2C9, 2D6, and 3A4, with IC50 values of > 30μM ( > 11.5μg/mL). Bortezomib may inhibit 2C19 activity (IC50 = 18 μM, 6.9 μg/mL) and increase exposure to drugs that are substrates for this enzyme. Bortezomib did not induce the activities of cytochrome P450 3A4 and 1A2 in primary cultured human hepatocytes.

Animal Toxicology and/or Pharmacology

Cardiovascular Toxicity

Studies in monkeys showed that administration of dosages approximately twice the recommended clinical dose resulted in heart rate elevations, followed by profound progressive hypotension, bradycardia, and death 12 to 14 hours post dose. Doses ≥ 1.2 mg/m²induced dose-proportional changes in cardiac parameters. Bortezomib has been shown to distribute to most tissues in the body, including the myocardium. In a repeated dosing toxicity study in the monkey, myocardial hemorrhage, inflammation, and necrosis were also observed.

Chronic Administration

In animal studies at a dose and schedule similar to that recommended for patients (twice weekly dosing for 2 weeks followed by 1-week rest), toxicities observed included severe anemia and thrombocytopenia, and gastrointestinal, neurological and lymphoid system toxicities. Neurotoxic effects of bortezomib in animal studies included axonal swelling and degeneration in peripheral nerves, dorsal spinal roots, and tracts of the spinal cord. Additionally, multifocal hemorrhage and necrosis in the brain, eye, and heart were observed.

Clinical Studies

Multiple Myeloma

Randomized, Open-Label Clinical Study in Patients with Previously Untreated Multiple Myeloma

A prospective, international, randomized (1:1), open-label clinical study of 682 patients was conducted to determine whether VELCADE administered intravenously (1.3 mg/m²) in combination with melphalan (9 mg/m²) and prednisone (60 mg/m²) resulted in improvement in time to progression (TTP) when compared to melphalan (9 mg/m²) and prednisone (60 mg/m²) in patients with previously untreated multiple myeloma. Treatment was administered for a maximum of 9 cycles (approximately 54 weeks) and was discontinued early for disease progression or unacceptable toxicity. Antiviral prophylaxis was recommended for patients on the VELCADE study arm.

The median age of the patients in the study was 71 years (48;91), 50% were male, 88% were Caucasian and the median Karnofsky performance status score for the patients was 80 (60;100). Patients had IgG/IgA/Light chain myeloma in 63%/25%/8% instances, a median hemoglobin of 105 g/L (64;165), and a median platelet count of 221,500 /microliter (33,000;587,000).

Efficacy results for the trial are presented in Table 11. At a pre-specified interim analysis (with median follow-up of 16.3 months), the combination of VELCADE, melphalan and prednisone therapy resulted in significantly superior results for time to progression, progression-free survival, overall survival and response rate. Further enrollment was halted, and patients receiving melphalan and prednisone were offered VELCADE in addition. A later, pre-specified analysis of overall survival (with median follow-up of 36.7 months with a hazard ratio of 0.65, 95% CI: 0.51, 0.84) resulted in a statistically significant survival benefit for the VELCADE, melphalan and prednisone treatment arm despite subsequent therapies including VELCADE based regimens. In an updated analysis of overall survival based on 387 deaths (median follow-up 60.1 months), the median overall survival for the VELCADE, melphalan and prednisone treatment arm was 56.4 months and for the melphalan and prednisone treatment arm was 43.1 months, with a hazard ratio of 0.695 (95% CI: 0.57, 0.85).

Table 11: Summary of Efficacy Analyses in the Previously Untreated Multiple Myeloma Study

Efficacy Endpoint VELCADE,
Melphalan and Prednisone
n=344
Melphalan and Prednisone
n=338
Time to Progression
Events n (%) 101 (29) 152 (45)
Mediana (months) (95% CI) 20.7 (17.6, 24.7) 15.0 (14.1, 17.9)
Hazard ratiob(95% CI) 0.54 (0.42, 0.70)
p-value c 0.000002
Progression-free Survival
Events n (%) 135 (39) 190 (56)
Mediana (months) (95% CI) 18.3 (16.6, 21.7) 14.0 (11.1, 15.0)
Hazard ratiob (95% CI) 0.61 (0.49, 0.76)
p-value c 0.00001
Response Rate
CRd n (%) 102 (30) 12 (4)
PRd n (%) 136 (40) 103 (30)
nCR n (%) 5 (1) 0
CR + PRd n (%) 238 (69) 115 (34)
p-valuee < 10-10
Overall Survival at median follow up of 36.7 months
Events (deaths) n (%) 109 (32) 148 (44)
Mediana (months) (95% CI) Not Reached (46.2, NR) 43.1 (34.8, NR)
Hazard ratiob (95% CI) 0.65 (0.51, 0.84)
p-value c 0.00084
Note: All results are based on the analysis performed at a median follow-up duration of 16.3 months except for the overall survival analysis.
aKaplan-Meier estimate
bHazard ratio estimate is based on a Cox proportional-hazard model adjusted for stratification factors: beta2-microglobulin, albumin, and region. A hazard ratio less than 1 indicates an advantage for VELCADE, melphalan and prednisone
cp-value based on the stratified log-rank test adjusted for stratification factors: beta2-microglobulin, albumin, and region
dEBMT criteria
ep-value for Response Rate (CR + PR) from the Cochran-Mantel-Haenszel chi-square test adjusted for the stratification factors

TTP was statistically significantly longer on the VELCADE, melphalan and prednisone arm (see Figure 1). (median follow-up 16.3 months)

Figure 1: Time to Progression
VELCADE, Melphalan and Prednisone versus Melphalan and Prednisone

Time to ProgressionVELCADE, Melphalan and Prednisone versus Melphalan and Prednisone - Illustration

Overall survival was statistically significantly longer on the VELCADE, melphalan and prednisone arm (see Figure 2). Median follow – up 60.1 months)

Figure 2 : Overall Survival
VELCADE, Melphalan and Prednisone versus Melphalan and Prednisone

Overall Survival  - Illustration

Randomized, Clinical Study in Relapsed Multiple Myeloma of VELCADE versus Dexamethasone

A prospective phase 3, international, randomized (1:1), stratified, open-label clinical study enrolling 669 patients was designed to determine whether VELCADE resulted in improvement in time to progression (TTP) compared to high-dose dexamethasone in patients with progressive multiple myeloma following 1 to 3 prior therapies. Patients considered to be refractory to prior high-dose dexamethasone were excluded as were those with baseline Grade ≥ 2 peripheral neuropathy or platelet counts < 50,000/μL. A total of 627 patients were evaluable for response.

Stratification factors were based on the number of lines of prior therapy the patient had previously received (1 previous line versus more than 1 line of therapy), time of progression relative to prior treatment (progression during or within 6 months of stopping their most recent therapy versus relapse > 6 months after receiving their most recent therapy), and screening β2-microglobulin levels ( ≤ 2.5 mg/L versus > 2.5 mg/L).

Baseline patient and disease characteristics are summarized in Table 12.

Table 12: Summary of Baseline Patient and Disease Characteristics in the Relapsed Multiple Myeloma Study

  VELCADE
N=333
Dexamethasone
N=336
Patient Characteristics
  Median age in years (range) 62.0 (33, 84) 61.0 (27, 86)
  Gender: Male/female 56% / 44% 60% / 40%
  Race: Caucasian/black/other 90% / 6% / 4% 88% / 7% / 5%
  Karnofsky performance status score ≤ 70 13% 17%
  Hemoglobin < 100 g/L 32% 28%
  Platelet count < 75 x 109/L 6% 4%
Disease Characteristics
  Type of myeloma (%):  IgG/IgA/Light chain 60% / 23% / 12% 59% / 24% / 13%
  Median p2-microglobulin (mg/L) 3.7 3.6
  Median albumin (g/L) 39.0 39.0
  Creatinine clearance ≤ 30 mL/min [n (%)] 17 (5%) 11 (3%)
Median Duration of Multiple Myeloma Since
  Diagnosis (Years) 3.5 3.1
Number of Prior Therapeutic Lines of Treatment
  Median 2 2
  1 prior line 40% 35%
   > 1 prior line 60% 65%
Previous Therapy
  Any prior steroids, e.g., dexamethasone, VAD 98% 99%
  Any prior anthracyclines, e.g., VAD, mitoxantrone 77% 76%
  Any prior alkylating agents, e.g., MP, VBMCP 91% 92%
  Any prior thalidomide therapy 48% 50%
  Vinca alkaloids 74% 72%
  Prior stem cell transplant/other high-dose therapy 67% 68%
  Prior experimental or other types of therapy 3% 2%

Patients in the VELCADE treatment group were to receive eight 3-week treatment cycles followed by three 5week treatment cycles of VELCADE. Patients achieving a CR were treated for 4 cycles beyond first evidence of CR. Within each 3-week treatment cycle, VELCADE 1.3 mg/m²/dose alone was administered by intravenous bolus twice weekly for 2 weeks on Days 1, 4, 8, and 11 followed by a 10-day rest period (Days 12 to 21).

Within each 5-week treatment cycle, VELCADE 1.3 mg/m²/dose alone was administered by intravenous bolus once weekly for 4 weeks on Days 1, 8, 15, and 22 followed by a 13-day rest period (Days 23 to 35) [see DOSAGE AND ADMINISTRATION].

Patients in the dexamethasone treatment group were to receive four 5-week treatment cycles followed by five 4week treatment cycles. Within each 5-week treatment cycle, dexamethasone 40 mg/day PO was administered once daily on Days 1 to 4, 9 to 12, and 17 to 20 followed by a 15-day rest period (Days 21-35). Within each 4week treatment cycle, dexamethasone 40 mg/day PO was administered once daily on Days 1 to 4 followed by a 24-day rest period (Days 5 to 28). Patients with documented progressive disease on dexamethasone were offered VELCADE at a standard dose and schedule on a companion study. Following a preplanned interim analysis of time to progression, the dexamethasone arm was halted and all patients randomized to dexamethasone were offered VELCADE, regardless of disease status.

In the VELCADE arm, 34% of patients received at least one VELCADE dose in all 8 of the 3-week cycles of therapy, and 13% received at least one dose in all 11 cycles. The average number of VELCADE doses during the study was 22, with a range of 1 to 44. In the dexamethasone arm, 40% of patients received at least one dose in all 4 of the 5-week treatment cycles of therapy, and 6% received at least one dose in all 9 cycles.

The time to event analyses and response rates from the relapsed multiple myeloma study are presented in Table 13. Response and progression were assessed using the European Group for Blood and Marrow Transplantation (EBMT) criteria. Complete response (CR) required < 5% plasma cells in the marrow, 100% reduction in M-protein, and a negative immunofixation test (IF-). Partial response (PR) requires ≥ 50% reduction in serum myeloma protein and ≥ 90% reduction of urine myeloma protein on at least 2 occasions for a minimum of at least 6 weeks along with stable bone disease and normal calcium. Near complete response (nCR) was defined as meeting all the criteria for complete response including 100% reduction in M-protein by protein electrophoresis; however, M-protein was still detectable by immunofixation (IF+).

Table 13: Summary of Efficacy Analyses in the Relapsed Multiple Myeloma Study

Efficacy Endpoint All Patients 1 Prior Line of Therapy > 1 Prior Line of Therapy
VELCADE
n=333
Dex
n=336
VELCADE
n=132
Dex
n=119
VELCADE
n=200
Dex
n=217
Time to Progression Events n (%) 147 (44) 196 (58) 55 (42) 64 (54) 92 (46) 132 (61)
Mediana (95% CI) 6.2 mo (4.9, 6.9) 3.5 mo (2.9, 4.2) 7.0 mo (6.2, 8.8) 5.6 mo (3.4, 6.3) 4.9 mo (4.2, 6.3) 2.9 mo (2.8, 3.5)
Hazard ratiob (95% CI) 0.55 (0.44, 0.69) 0.55 (0.38, 0.81) 0.54 (0.41, 0.72)
p-valuec < 0.0001 0.0019 < 0.0001
Overall Survival
Events (deaths) n (%) 51 (15) 84 (25) 12 (9) 24 (20) 39 (20) 60 (28)
Hazard ratiob (95% CI) 0.57 (0.40, 0.81) 0.39 (0.19, 0.81) 0.65 (0.43, 0.97)
p-valuec,d < 0.05 < 0.05 < 0.05
Response Rate Populatione n = 627 n=315 n=312 n=128 n=110 n=187 n=202
CRfn (%) 20 (6) 2 (<1) 8 (6) 2 (2) 12 (6) 0 (0)
PRf n(%) 101 (32) 54 (17) 49 (38) 27 (25) 52 (28) 27 (13)
nCRf,g n(%) 21 (7) 3 (<1) 8 (6) 2 (2) 13 (7) 1 (<1)
CR + PRf n (%) 121 (38) 56 (18) 57 (45) 29 (26) 64 (34) 27 (13)
p-valueh < 0.0001 0.0035 < 0.0001

aKaplan-Meier estimate
bHazard ratio is based on Cox proportional-hazard model with the treatment as single independent variable. A hazard ratio less than 1 indicates an advantage for VELCADE
cp-value based on the stratified log-rank test including randomization stratification factors
dPrecise p-value cannot be rendered
eResponse population includes patients who had measurable disease at baseline and received at least 1 dose of study drug
fEBMT criteria; nCR meets all EBMT criteria for CR but has positive IF. Under EBMT criteria nCR is in the PR category
gIn 2 patients, the IF was unknown
hp-value for Response Rate (CR + PR) from the Cochran-Mantel-Haenszel chi-square test adjusted for the stratification factors

TTP was statistically significantly longer on the VELCADE arm (see Figure 3).

Figure 3: Time to Progression
Bortezomib versus Dexamethasone (relapsed multiple myeloma study)

Time to Progression Bortezomib versus Dexamethasone - Illustration

As shown in Figure 4 VELCADE had a significant survival advantage relative to dexamethasone (p < 0.05). The median follow-up was 8.3 months.

Figure 4: Overall Survival
Bortezomib versus Dexamethasone (relapsed multiple myeloma study)

Overall Survival Bortezomib versus Dexamethasone -  Illustration

For the 121 patients achieving a response (CR or PR) on the VELCADE arm, the median duration was 8.0 months (95% CI: 6.9, 11.5 months) compared to 5.6 months (95% CI: 4.8, 9.2 months) for the 56 responders on the dexamethasone arm. The response rate was significantly higher on the VELCADE arm regardless of β2microglobulin levels at baseline.

Randomized, Open-Label Clinical Study of VELCADE Subcutaneous versus Intravenous in Relapsed Multiple Myeloma

An open-label, randomized, phase 3 non-inferiority study compared the efficacy and safety of the subcutaneous administration of VELCADE versus the intravenous administration. This study included 222 bortezomib naïve patients with relapsed multiple myeloma, who were randomized in a 2:1 ratio to receive 1.3 mg/m²of VELCADE by either the subcutaneous (n=148) or intravenous (n=74) route for 8 cycles. Patients who did not obtain an optimal response (less than Complete Response (CR)) to therapy with VELCADE alone after 4 cycles were allowed to receive oral dexamethasone 20 mg daily on the day of and after VELCADE administration (82 patients in subcutaneous treatment group and 39 patients in the intravenous treatment group). Patients with baseline Grade ≥ 2 peripheral neuropathy or neuropathic pain, or platelet counts < 50,000/μL were excluded. A total of 218 patients were evaluable for response.

Stratification factors were based on the number of lines of prior therapy the patient had received (1 previous line versus more than 1 line of therapy), and international staging system (ISS) stage (incorporating beta2-microglobulin and albumin levels; Stages I, II, or III).

The baseline demographic and others characteristics of the two treatment groups are summarized as follows: the median age of the patient population was approximately 64 years of age (range 38-88 years), primarily male (subcutaneous: 50%, intravenous: 64%); the primary type of myeloma is IgG (subcutaneous: 65% IgG, 26% IgA, 8% light chain; intravenous: 72% IgG, 19% IgA, 8% light chain), ISS staging I/II/III (%) was 27, 41, 32 for both subcutaneous and intravenous, Karnofsky performance status score was ≤ 70% in 22% of subcutaneous and 16% of intravenous, creatinine clearance was 67.5 mL/min in subcutaneous and 73 mL/min in intravenous, the median years from diagnosis was 2.68 and 2.93 in subcutaneous and intravenous respectively and the proportion of patients with more than one prior line of therapy was 38% in subcutaneous and 35% in intravenous.

This study met its primary (non-inferiority) objective that single agent subcutaneous VELCADE retains at least 60% of the overall response rate after 4 cycles relative to single agent intravenous VELCADE. The results are provided in Table 14.

Table 14: Summary of Efficacy Analyses in the Relapsed Multiple Myeloma Study of VELCADE Subcutaneous versus Intravenous

Intent to Treat Population Subcutaneous VELCADE
n=148
Intravenous VELCADE
n=74
Primary Endpoint
Response Rate at 4 cycles
    ORR (CR+PR) n(%) 63 (43) 31 (42)
  Ratio of Response Rates (95% CI) 1.01 (0.73, 1.40)
    CR n (%) 11 (7) 6 (8)
    PR n (%) 52 (35) 25 (34)
    nCR n (%) 9 (6) 4 (5)
Secondary Endpoints
Response Rate at 8 cycles
    ORR (CR+PR) 78 (53) 38 (51)
    CR n (%) 17 (11) 9 (12)
    PR n (%) 61 (41) 29 (39)
    nCR n (%) 14 (9) 7 (9)
Median Time to Progression, months 10.4 9.4
Median Progression Free Survival, months 10.2 8
1-year Overall Survival (%)a 72.6 76.7
a Median duration of follow up is 11.8 months

A Randomized Phase 2 Dose-Response Study in Relapsed Multiple Myeloma

An open-label, multicenter study randomized 54 patients with multiple myeloma who had progressed or relapsed on or after front-line therapy to receive VELCADE 1 mg/m²or 1.3 mg/m²intravenous bolus twice weekly for 2 weeks on Days 1, 4, 8, and 11 followed by a 10-day rest period (Days 12 to 21). The median duration of time between diagnosis of multiple myeloma and first dose of VELCADE on this trial was 2.0 years, and patients had received a median of 1 prior line of treatment (median of 3 prior therapies). A single complete response was seen at each dose. The overall response rates (CR + PR) were 30% (8/27) at 1 mg/m²and 38% (10/26) at 1.3 mg/m².

A Phase 2 Open-Label Extension Study in Relapsed Multiple Myeloma

Patients from the two phase 2 studies, who in the investigators' opinion would experience additional clinical benefit, continued to receive VELCADE beyond 8 cycles on an extension study. Sixty-three (63) patients from the phase 2 multiple myeloma studies were enrolled and received a median of 7 additional cycles of VELCADE therapy for a total median of 14 cycles (range 7 to 32). The overall median dosing intensity was the same in both the parent protocol and extension study. Sixty-seven percent (67%) of patients initiated the extension study at the same or higher dose intensity at which they completed the parent protocol, and 89% of patients maintained the standard 3-week dosing schedule during the extension study. No new cumulative or new long-term toxicities were observed with prolonged VELCADE treatment [see ADVERSE REACTIONS].

Mantle Cell Lymphoma

A Phase 2 Single-arm Clinical Study in Relapsed Mantle Cell Lymphoma After Prior Therapy

The safety and efficacy of VELCADE in relapsed or refractory mantle cell lymphoma were evaluated in an open-label, single-arm, multicenter study of 155 patients with progressive disease who had received at least 1 prior therapy. The median age of the patients was 65 years (42, 89), 81% were male, and 92% were Caucasian. Of the total, 75% had one or more extra-nodal sites of disease, and 77% were stage 4. In 91% of the patients, prior therapy included all of the following: an anthracycline or mitoxantrone, cyclophosphamide, and rituximab. A total of thirty seven percent (37%) of patients were refractory to their last prior therapy. An intravenous bolus injection of VELCADE 1.3 mg/m²/dose was administered twice weekly for 2 weeks on Days 1, 4, 8, and 11 followed by a 10-day rest period (Days 12 to 21) for a maximum of 17 treatment cycles. Patients achieving a CR or CRu were treated for 4 cycles beyond first evidence of CR or CRu. The study employed dose modifications for toxicity [see DOSAGE AND ADMINISTRATION].

Responses to VELCADE are shown in Table 15. Response rates to VELCADE were determined according to the International Workshop Response Criteria (IWRC) based on independent radiologic review of CT scans. The median number of cycles administered across all patients was 4; in responding patients the median number of cycles was 8. The median time to response was 40 days (range 31 to 204 days). The median duration of follow-up was more than 13 months.

Table 15: Response Outcomes in a Phase 2 Mantle Cell Lymphoma Study

Response Analyses (N = 155) N (%) 95% CI
Overall Response Rate (IWRC) (CR + CRu + PR) 48 (31) (24, 39)
  Complete Response (CR + CRu) 12 (8) (4, 13)
     CR 10 (6) (3, 12)
     CRu 2 (1) (0, 5)
  Partial Response (PR) 36 (23) (17, 31)
Duration of Response Median 95% CI
     CR + CRu + PR (N = 48) 9.3 months (5.4, 13.8)
     CR + CRu (N = 12) 15.4 months (13.4, 15.4)
     PR (N=36) 6.1 months (4.2, 9.3)

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

PATIENT INFORMATION

Physicians are advised to discuss the following with patients prior to treatment with VELCADE:

Ability to Drive or Operate Machinery or Impairment of Mental Ability

VELCADE may cause fatigue, dizziness, syncope, orthostatic/postural hypotension. Advise patients not to drive or operate machinery if they experience any of these symptoms.

Dehydration/Hypotension

Patients receiving VELCADE therapy may experience vomiting and/or diarrhea. Advise patients how to avoid dehydration. Instruct patients to seek medical advice if they experience symptoms of dizziness, light headedness or fainting spells.

Pregnancy/Nursing

Advise patients to use effective contraceptive measures to prevent pregnancy during treatment with VELCADE. Instruct patients to report pregnancy to their physicians immediately. Advise patients that they should not receive VELCADE while pregnant or breast-feeding. If a patient wishes to restart breastfeeding after treatment, she should be advised to discuss the appropriate timing with her physician.

Concomitant Medications

Advise patients to speak with their physicians about any other medication they are currently taking.

Diabetic Patients

Advise patients to check their blood sugar frequently if using an oral antidiabetic medication and to notify their physicians of any changes in blood sugar level.

Peripheral Neuropathy

Advise patients to contact their physicians if they experience new or worsening symptoms of peripheral neuropathy such as tingling, numbness, pain, a burning feeling in the feet or hands, or weakness in the arms or legs.

Other

Instruct patients to contact their physicians if they develop a rash, experience shortness of breath, cough, or swelling of the feet, ankles, or legs, convulsion, persistent headache, reduced eyesight, an increase in blood pressure or blurred vision.

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

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PATIENT INFORMATION

Physicians are advised to discuss the following with patients prior to treatment with VELCADE:

Ability to Drive or Operate Machinery or Impairment of Mental Ability

VELCADE may cause fatigue, dizziness, syncope, orthostatic/postural hypotension. Advise patients not to drive or operate machinery if they experience any of these symptoms.

Dehydration/Hypotension

Patients receiving VELCADE therapy may experience vomiting and/or diarrhea. Advise patients how to avoid dehydration. Instruct patients to seek medical advice if they experience symptoms of dizziness, light headedness or fainting spells.

Pregnancy/Nursing

Advise patients to use effective contraceptive measures to prevent pregnancy during treatment with VELCADE. Instruct patients to report pregnancy to their physicians immediately. Advise patients that they should not receive VELCADE while pregnant or breast-feeding. If a patient wishes to restart breastfeeding after treatment, she should be advised to discuss the appropriate timing with her physician.

Concomitant Medications

Advise patients to speak with their physicians about any other medication they are currently taking.

Diabetic Patients

Advise patients to check their blood sugar frequently if using an oral antidiabetic medication and to notify their physicians of any changes in blood sugar level.

Peripheral Neuropathy

Advise patients to contact their physicians if they experience new or worsening symptoms of peripheral neuropathy such as tingling, numbness, pain, a burning feeling in the feet or hands, or weakness in the arms or legs.

Other

Instruct patients to contact their physicians if they develop a rash, experience shortness of breath, cough, or swelling of the feet, ankles, or legs, convulsion, persistent headache, reduced eyesight, an increase in blood pressure or blurred vision.

Last reviewed on RxList: 11/6/2012
This monograph has been modified to include the generic and brand name in many instances.

Disclaimer

Velcade Consumer

IMPORTANT: HOW TO USE THIS INFORMATION: This is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate for you. This information is not individual medical advice and does not substitute for the advice of your health care professional. Always ask your health care professional for complete information about this product and your specific health needs.

BORTEZOMIB - INJECTION

(bor-TEZ-oh-mib)

COMMON BRAND NAME(S): Velcade

USES: This medication is a cancer chemotherapy drug used to treat certain types of tumors (e.g., multiple myeloma). It blocks certain proteins which helps to slow the growth and spread of the cancer.

HOW TO USE: This medication is given by injection into a vein or under the skin by a healthcare professional. If you are receiving this medication under the skin, make sure that the injection site is changed each time to lessen injury under the skin. The dosage is based on your body size, medical condition, and response to therapy.

It is important to drink plenty of fluids while you are being treated with this drug to prevent becoming dehydrated. Read the Patient Information Leaflet that comes with this drug, and consult your doctor or pharmacist if you have any questions.

Disclaimer

Velcade Consumer (continued)

SIDE EFFECTS: Dizziness, lightheadedness, nausea, vomiting, loss of appetite, diarrhea, constipation, tiredness, weakness, blurred vision, or pain/redness at injection site may occur. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

This medication can lower your body's ability to fight an infection. Notify your doctor promptly if you develop any signs of an infection such as fever, chills, or persistent sore throat.

Tell your doctor right away if you have any serious side effects, including: easy bruising or bleeding, tingling/numbness/pain/burning feeling of the hands or feet (peripheral neuropathy), fainting, stomach pain, black stools, coffee-ground vomit, trouble breathing, swelling or pain in the lower legs, fast/irregular heartbeat, severe headache, vision problems, mental/mood changes (e.g., rarely, thoughts of suicide), swelling of the hands/ankles/feet, change in the amount of urine, yellowing skin/eyes, dark urine.

Get medical help right away if any of these rare but very serious side effects occur: chest pain, weakness on one side of the body, slurred speech, seizures.

An allergic reaction to this drug is unlikely, but get medical help right away if it occurs. Symptoms of an allergic reaction include: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

In the US -

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Read the Velcade (bortezomib) Side Effects Center for a complete guide to possible side effects »

PRECAUTIONS: Before using this medication, tell your doctor or pharmacist if you are allergic to it; or if you have any other allergies. This product may contain inactive ingredients (such as boron, mannitol), which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Before using this medication, tell your doctor or pharmacist your medical history, especially of: nerve sensation problems (e.g., peripheral neuropathy), heart disease, low blood pressure, loss of body fluids (dehydration), diabetes, liver disease, severe kidney disease, certain viral infection (herpes, shingles).

To minimize dizziness and lightheadedness, get up slowly when rising from a seated or lying position.

This drug may make you dizzy or cause vision changes. Do not drive, use machinery, or do any activity that requires alertness or clear vision until you are sure you can perform such activities safely. Limit alcoholic beverages.

Do not have immunizations/vaccinations without the consent of your doctor and avoid contact with people who have recently received oral polio vaccine.

Use caution with sharp objects like safety razors or nail cutters and avoid activities such as contact sports to lower the chance of getting cut, bruised, or injured.

Wash your hands well to prevent the spread of infections.

This medication is not recommended for use during pregnancy. It may cause harm to an unborn baby. Discuss the risks and benefits with your doctor. If you become pregnant or think you may be pregnant, inform your doctor immediately. Use reliable form(s) of birth control during treatment with this drug. Consult your doctor for more details.

It is not known whether this drug passes into breast milk. Breast-feeding is not recommended while using this drug due to the potential risk to the nursing infant. Consult your doctor before breast-feeding.

Disclaimer

Velcade Consumer (continued)

DRUG INTERACTIONS: Drug interactions may change how your medications work or increase your risk for serious side effects. This document does not contain all possible drug interactions. Keep a list of all the products you use (including prescription/nonprescription drugs and herbal products) and share it with your doctor and pharmacist. Do not start, stop, or change the dosage of any medicines without your doctor's approval.

Some products that may interact with this drug include: medications to treat high blood pressure, oral anti-diabetic drugs, other drugs that may cause peripheral neuropathy (e.g., amiodarone, isoniazid, nitrofurantoin, certain anti-virals such as acyclovir, ritonavir, zidovudine).

Other medications can affect the removal of bortezomib from your body, which may affect how bortezomib works. Examples include azole antifungals (such as ketoconazole), macrolide antibiotics (such as erythromycin), rifamycins (such as rifabutin), St. John's wort, drugs used to treat seizures (such as carbamazepine, phenytoin), among others.

OVERDOSE: If overdose is suspected, contact your local poison control center or emergency room immediately. US residents can call the US national poison hotline at 1-800-222-1222. Canadian residents should call their local poison control center directly. Symptoms of overdose may include: fainting or persistent fever.

NOTES: Laboratory and/or medical tests (e.g., complete blood counts, platelets) should be performed periodically to monitor your progress or check for side effects. Consult your doctor for more details.

MISSED DOSE: For the best possible benefit, it is important to receive each scheduled dose of this medication as directed. If you miss a dose, contact your doctor or pharmacist immediately to establish a new dosing schedule.

STORAGE: Not applicable. This medication is given in a clinic and will not be stored at home.

MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854- 1166 (USA) or 1-800-668-1507 (Canada).

Information last revised March 2012. Copyright(c) 2012 First Databank, Inc.

Velcade Patient Information Including Side Effects

Brand Names: Velcade

Generic Name: bortezomib (Pronunciation: bor TEZ oh mib)

What is bortezomib (Velcade)?

Bortezomib interferes with the growth of some cancer cells and keeps them from spreading in your body.

Bortezomib is used to treat multiple myeloma and mantle cell lymphoma.

Bortezomib is sometimes given after other cancer medications have been tried without successful treatment.

Bortezomib may also be used for purposes not listed in this medication guide.

What are the possible side effects of bortezomib (Velcade)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have a serious side effect such as:

  • new or worsening nerve problems such as numbness, burning, pain, weakness, or tingly feeling;
  • feeling like you might pass out;
  • dry cough and trouble breathing;
  • severe headache, vision problems, confusion, and/or seizure (convulsions);
  • black, bloody, or tarry stools, vomit that looks like blood or coffee grounds;
  • severe constipation;
  • easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin;
  • fever, chills, body aches, flu symptoms;
  • red bumps, spreading skin rash, painful skin lesions on your arms, face, or neck;
  • feeling short of breath, even with mild exertion;
  • fast or slow heart rate, weak pulse, lower back pain, blood in your urine;
  • urinating less than usual or not at all;
  • muscle weakness, tightness, or contraction, overactive reflexes; or
  • nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).

Less serious side effects may include:

  • mild nausea, vomiting, upset stomach;
  • diarrhea, constipation, bloating;
  • headache, mild dizziness;
  • muscle pain, bone or joint pain;
  • sleep problems (insomnia);
  • mild rash or itching; or
  • skin irritation where the medicine was injected.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Read the Velcade (bortezomib) Side Effects Center for a complete guide to possible side effects »

What is the most important information I should know about bortezomib (Velcade)?

Bortezomib can lower blood cells that help your body fight infections. Your blood may need to be tested often. Avoid being near people who are sick or have infections. Avoid activities that may increase your risk of bleeding injury. Tell your doctor at once if you develop signs of infection.

Avoid becoming dehydrated if you have any vomiting or diarrhea. Symptoms of dehydration include dizziness, dry mouth, fainting, or hot and dry skin. Talk with your doctor about how best to keep yourself hydrated.

This medication may cause blurred vision and may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert and able to see clearly.

Side Effects Centers

Velcade Patient Information including How Should I Take

What should I discuss with my healthcare provider before receiving bortezomib (Velcade)?

You should not use this medication if you are allergic to bortezomib, mannitol, or boron.

To make sure you can safely receive bortezomib, tell your doctor if you have any of these other conditions:

  • diabetes;
  • liver disease;
  • kidney disease, or if you are on dialysis;
  • a bleeding or blood clotting disorder;
  • a low level of platelets or white or red blood cells;
  • heart disease, congestive heart failure;
  • herpes or a history of shingles;
  • high or low blood pressure; or
  • nerve problems such as numbness, burning, pain, or tingly feeling.

FDA pregnancy category D. Do not use bortezomib if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

It is not known whether bortezomib passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are using bortezomib.

How is bortezomib given (Velcade)?

Bortezomib is injected into a vein through an IV.

You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare provider will give you this injection.

Bortezomib is usually injected 2 times a week for 2 weeks, followed by 10 days without an injection. Bortezomib may also be given once a week for 4 weeks followed by 13 days without an injection. Follow your doctor's instructions about your individual dosing schedule.

Bortezomib can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. Your blood may need to be tested often. Your liver function may also need to be tested. Visit your doctor regularly.

Side Effects Centers

Velcade Patient Information including If I Miss a Dose

What happens if I miss a dose (Velcade)?

Call your doctor for instructions if you will miss an appointment for your bortezomib injection.

What happens if I overdose (Velcade)?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose may cause weakness, bruising or bleeding, pinpoint red spots on your skin, and fainting.

What should I avoid while receiving bortezomib (Velcade)?

Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.

This medication may cause blurred vision and may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert and able to see clearly.

Avoid becoming dehydrated if you have any vomiting or diarrhea. Symptoms of dehydration include dizziness, dry mouth, fainting, or hot and dry skin. Talk with your doctor about how best to keep yourself hydrated.

Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall.

What other drugs will affect bortezomib (Velcade)?

Many drugs can interact with bortezomib. Below is just a partial list. Tell your doctor if you are using:

  • dexamethasone (Decadron, Hexadrol);
  • rifabutin (Mycobutin), rifampin (Rifadin, Rifater, Rifamate), or rifapentine (Priftin);
  • St. John's wort;
  • an antibiotic such as clarithromycin (Biaxin), erythromycin (E.E.S., EryPed, Ery-Tab, Erythrocin, Pediazole), or telithromycin (Ketex);
  • an antifungal medication such as clotrimazole (Mycelex Troche), itraconazole (Sporanox), ketoconazole (Nizoral), miconazole (Oravig), or voriconazole (Vfend);
  • an antidepressant such as nefazodone, paroxetine (Paxil), or sertraline (Zoloft);
  • a barbiturate such as amobarbital (Amytal), butabarbital (Butisol), mephobarbital (Mebaral), secobarbital (Seconal), or phenobarbital (Solfoton);
  • diabetes medicine you take by mouth (your dose may need to be adjusted when your bortezomib treatment starts);
  • HIV/AIDS medicine such as atazanavir (Reyataz), delavirdine (Rescriptor), efavirenz (Sustiva, Atripla), etravirine (Intelence), indinavir (Crixivan), nelfinavir (Viracept), nevirapine (Viramune), saquinavir (Invirase), or ritonavir (Norvir, Kaletra);
  • medicines to treat narcolepsy, such as armodafanil (Nuvigil) or modafanil (Progivil); or
  • seizure medicine such as carbamazepine (Carbatrol, Equetro, Tegretol), felbamate (Felbatol), oxcarbazepine (Trileptal), or phenytoin (Dilantin), or primidone (Mysoline).

This list is not complete and other drugs may interact with bortezomib. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.

Where can I get more information?

Your pharmacist can provide more information about bortezomib.


Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2012 Cerner Multum, Inc. Version: 7.01. Revision date: 8/12/2011.

Your use of the content provided in this service indicates that you have read,understood and agree to the End-User License Agreement,which can be accessed by clicking on this link.

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Side Effects Centers

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