Regimen Reference Order MYEL daratumumab + bortezomib + dexamethasone (DVd) ARIA: MYEL - [DVd]

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Updated: January 8, 2019 Regimen Reference Order MYEL daratumumab + bortezomib + dexamethasone (DVd) ARIA: MYEL - [DVd] Planned Course: Indication for Use: CVAD: At Provider s Discretion Proceed with treatment if: of every cycle bortezomib: Every 28 days until disease progression or unacceptable toxicity Relapsed Multiple Myeloma ANC equal to or greater than 1 x 10 9 /L AND Platelets equal to or greater than 30 x 10 9 /L daratumumab: On, proceed with daratumumab only when bortezomib starts On subsequent treatment days, proceed with daratumumab regardless of blood counts 5 of Cycles 1 and 2 only bortezomib: ANC equal to or greater than 1 x 10 9 /L AND Platelets equal to or greater than 30 x 10 9 /L Contact Hematologist if parameters not met SEQUENCE OF MEDICATION ADMINISTRATION Pre-treatment Requirements montelukast 10 mg Orally once daily in the morning for 5 days, starting the day before each daratumumab dose of Cycle 1 Cycle 2 onwards at the discretion of the physician *Nursing Alert: Notify physician if patient has not taken montelukast Treatment Regimen Establish primary solution 500 ml of: normal saline Cycle 1 acetaminophen 975 mg Orally 1 hour prior to daratumumab on Days 1, 2, 8, 15 and 22 daratumumab on Days 1, 2, 8, 15 and 22 daratumumab on Days 1, 2, 8, 15 and 22 Please refer to CCMB Formulary for Criteria for Use Page 1 of 5

daratumumab 8 mg/kg IV in normal saline 500 ml on Days 1 and 2 0 to 60 minutes 50 ml/hour 60 to 120 minutes 100 ml/hour 120 to 180 minutes 150 ml/hour 180 minutes onwards 200 ml/hour 16 mg/kg IV in normal saline 500 ml on Day 8 0 to 60 minutes 50 ml/hour 60 to 120 minutes 100 ml/hour 120 to 180 minutes 150 ml/hour 180 minutes onwards 200 ml/hour 16 mg/kg IV in normal saline 500 ml on Days 15 and 22 dexamethasone 20 mg Orally once daily in the morning on Days 9, 16 and 23 Cycle 2 acetaminophen 975 mg Orally 1 hour prior to daratumumab on Days 1, 8, 15 and 22 daratumumab on Days 1, 8, 15 and 22 daratumumab on Days 1, 8, 15 and 22 daratumumab 16 mg/kg IV in normal saline 500 ml on Days 1, 8, 15 and 22 dexamethasone 20 mg Orally once daily in the morning on Days 2, 9, 16 and 23 Please refer to CCMB Formulary for Criteria for Use Page 2 of 5

Cycles 3 and 4 acetaminophen 975 mg Orally 1 hour prior to daratumumab on Days 1 and 15 daratumumab on Days 1 and 15 daratumumab on Days 1 and 15 daratumumab 16 mg/kg IV in normal saline 500 ml on Days 1 and 15 dexamethasone 20 mg Orally once daily in the morning on Days 2 and 16 dexamethasone 40 mg Orally once daily in the morning on Days 8 and 22 Cycles 5 to 8 acetaminophen 975 mg Orally 1 hour prior to daratumumab on daratumumab on daratumumab on daratumumab 16 mg/kg IV in normal saline 500 ml on 0 to 60 minutes 100 ml/hour 60 to 120 minutes 150 ml/hour 120 minutes onwards - 200 ml/hour dexamethasone 20 mg Orally once daily in the morning on Day 2 dexamethasone 40 mg Orally once daily in the morning on Days 8, 15 and 22 Cycle 9* and onwards acetaminophen 975 mg Orally 1 hour prior to daratumumab daratumumab daratumumab Please refer to CCMB Formulary for Criteria for Use Page 3 of 5

daratumumab 16 mg/kg IV in normal saline 500 ml on only dexamethasone 20 mg Orally once daily in the morning on Day 2 * At physician s discretion, bortezomib may be prescribed Cycles 9 and onwards as maintenance on Days 1 and 15 All doses will be automatically rounded that fall within the DSG Approved Dose Bands. See LYMP DSG Dose Banding document for more information Flush after each medication: 50 ml over 6 minutes (500 ml/hr) In the event of an infusion-related hypersensitivity reaction, refer to the Hypersensitivity Reaction Standing Order REQUIRED MONITORING Baseline RBC serology (genotyping) mandatory prior to starting daratumumab Cycles 1 and 2 CBC, biochemistry, as per Physician Orders SPEP/FLCI (response assessment) 5 CBC Days 8 and 22 No blood work required Cycles 3 to 6 CBC, biochemistry as per physician order SPEP/FLCI (response assessment) Days 8, 15 and 22 No blood work required Cycle 7 and onwards CBC, biochemistry as per Physician Orders SPEP/FLCI (response assessment) Please refer to CCMB Formulary for Criteria for Use Page 4 of 5

daratumumab monitoring Cycle 1, Days 1 and 2 Full vital signs (temperature, heart rate, respiration, blood pressure and O 2 saturation) o at baseline, then o blood pressure and pulse every 15 minutes for 1 hour, then o blood pressure and pulse every 30 minutes for 1 hour, then o blood pressure and pulse every hour until infusion complete Subsequent Doses Full vital signs at baseline and then as clinically indicated Observation periods No observation periods. Patient can be discharged from treatment room if stable whether they had a reaction or not Recommended Support Medications valacylovir 500 mg Orally once daily prednisone 25 mg Orally once daily in the morning the day after daratumumab on Day 3 of first cycle only Alert: prednisone is prescribed to prevent delayed infusion reactions (respiratory) salmeterol and fluticasone combination (Advair Diskus) DISCHARGE INSTRUCTIONS 100 mcg - 50 mcg per dose Diskus inhaler Prescribed at physician s discretion If patient has a history of asthma or COPD, inhale 1 puff twice daily only as needed post infusion Remind patient to take prednisone and dexamethasone at home Advise patient to avoid green tea to prevent interactions with bortezomib Reinforce applicable safe handling precautions of medications, blood and body fluids for 48 hours after completion of chemotherapy ADDITIONAL INFORMATION Consideration may be given to reducing dexamethasone dose at the physician s discretion; to 20 mg for patients older than 75 years or have a body-mass index of less than 18.5 daratumumab interferes with cross-matching and red blood cell antibody screening. If a transfusion in required, draw Type and Screen and indicate on requisition that the patient is on daratumumab. The nurse must indicate each time, in case it was missed previously All patients should be considered for bisphosphonate therapy Administering nurse must document any infusion-related reactions with any dose of daratumumab Administration site restrictions are in place for daratumumab. Cycle 1 must be administered at CCMB MacCharles in Winnipeg. Cycle 2 onwards should only be administered at a site in which a pharmacy is on site Please refer to CCMB Formulary for Criteria for Use Page 5 of 5