Berenson James R, Cartmell Alan, Bessudo Alberto, Lyons Roger M, Harb Wael, Tzachanis Dimitrios, Agajanian Richy, Boccia Ralph, Coleman Morton, Moss Robert A, Rifkin Robert M, Patel Priti, Dixon Sandra, Ou Ying, Anderl Janet, Aggarwal Sanjay, Berdeja Jesus G
Institute for Myeloma and Bone Cancer Research, West Hollywood, CA;
Comprehensive Blood and Cancer Center, Bakersfield, CA;
Blood. 2016 Jun 30;127(26):3360-8. doi: 10.1182/blood-2015-11-683854. Epub 2016 May 12.
Carfilzomib, a proteasome inhibitor, is approved in the United States as a single agent, and in combination with dexamethasone or lenalidomide/dexamethasone (KRd) for relapsed or refractory multiple myeloma (MM). Under the single-agent and KRd approvals, carfilzomib is administered as a 10-minute IV infusion on days 1, 2, 8, 9, 15, and 16 of 28-day cycles (20 mg/m(2) [cycle 1, days 1-2]; 27 mg/m(2) thereafter). This multicenter, single-arm, phase 1/2 study, Community Harmonized Assessment of Myeloma Patients via an Integrated Oncology Network-1 (CHAMPION-1), evaluated once-weekly carfilzomib with dexamethasone in relapsed, or relapsed and refractory MM (1-3 prior therapies). Patients received carfilzomib (30-minute IV infusion) on days 1, 8, and 15 of 28-day cycles. The phase 1 portion used a 3 + 3 dose-escalation scheme to determine the maximum tolerated dose (MTD) of carfilzomib. During phase 2, patients received carfilzomib on the same schedule at the MTD. Patients received dexamethasone (40 mg) on days 1, 8, 15, and 22; dexamethasone was omitted on day 22 for cycles 9+. A total of 116 patients were enrolled. The MTD was 70 mg/m(2), and 104 patients (phase 1/2) received carfilzomib 70 mg/m(2) At 70 mg/m(2), the median number of prior regimens was 1; and 52% were bortezomib-refractory. At 70 mg/m(2), the most common grade ≥3 adverse events were fatigue (11%) and hypertension (7%). Overall response rate at 70 mg/m(2) was 77%. Median progression-free survival was 12.6 months. These findings merit additional evaluation of the once-weekly dosing regimen. This trial was registered at www.clinicaltrials.gov as #NCT01677858.
卡非佐米是一种蛋白酶体抑制剂,在美国被批准作为单一药物使用,也可与地塞米松或来那度胺/地塞米松(KRd)联合用于复发或难治性多发性骨髓瘤(MM)。在单一药物和KRd的批准方案下,卡非佐米在28天周期的第1、2、8、9、15和16天进行10分钟的静脉输注(第1周期第1 - 2天为20mg/m²;此后为27mg/m²)。这项多中心、单臂、1/2期研究,即通过综合肿瘤学网络对骨髓瘤患者进行社区统一评估-1(CHAMPION-1),评估了复发或复发难治性MM(1 - 3线既往治疗)患者中卡非佐米与地塞米松每周一次的联合用药情况。患者在28天周期的第1、8和15天接受卡非佐米(30分钟静脉输注)。1期部分采用3 + 3剂量递增方案来确定卡非佐米的最大耐受剂量(MTD)。在2期,患者按MTD的相同给药方案接受卡非佐米治疗。患者在第1、8、15和22天接受地塞米松(40mg);从第9周期开始,第22天省略地塞米松。共入组116例患者。MTD为70mg/m²,104例患者(1/2期)接受70mg/m²的卡非佐米治疗。在70mg/m²剂量下,既往治疗方案的中位数为1种;52%的患者对硼替佐米耐药。在70mg/m²剂量下,最常见的≥3级不良事件为疲劳(11%)和高血压(7%)。70mg/m²剂量下的总体缓解率为77%。中位无进展生存期为12.6个月。这些发现值得对每周一次给药方案进行进一步评估。该试验在www.clinicaltrials.gov上注册,编号为#NCT01677858。