Personalized Therapy for Multiple Myeloma by Saad Z. Usmani & Ajay K. Nooka

Personalized Therapy for Multiple Myeloma by Saad Z. Usmani & Ajay K. Nooka

Author:Saad Z. Usmani & Ajay K. Nooka
Language: eng
Format: epub
Publisher: Springer International Publishing, Cham


5.9.1.2 Carfilzomib, Cyclophosphamide, and Dexamethasone (CCyD)

Carfilzomib has also been combined with cyclophosphamide and dexamethasone as a treatment regimen in a phase II study newly diagnosed patients who were not transplant eligible [86]. In this study, carfilzomib was given on a standard schedule on days 1, 2, 8, 9, 15, and 16 on a 28-day cycle at 20 mg/m2 on days 1 and 2 of cycle 1 and then 36 mg/m2 subsequently. Cyclophosphamide 300 mg/m2 orally was given on days 1, 8, and 15, and dexamethasone 40 mg was given orally on days 1, 8, 15, and 22. This study found a high response rate with an ORR of 95% and 20% stringent CR. In this older, transplant-ineligible patient population, the adverse event rate was comparable to other regimens, with grade ≥3 neutropenia (20%) and anemia (11%) and cardiopulmonary adverse events (7%). This regimen is currently being evaluated in patients after one prior line of treatment and compared to CyBorD in the Myeloma UK five study [87]. In this study, the dosing is similar to the regimen in newly diagnosed patients, though cyclophosphamide is given at 500 mg. Preliminary toxicity data has been presented so far, with grade ≥3 hematologic adverse events including anemia (19.4%), neutropenia (12%), and thrombocytopenia (10.5%) and non-hematologic ≥ grade 3 including infections (20.9%).



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