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Efficacy of VDT PACE-like regimens in treatment of relapsed/refractory multiple myeloma

机译:VDT步伐状方案治疗复发/难治多发性骨髓瘤的疗效

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Experience with intensive chemotherapy for relapsed/refractory multiple myeloma (RRMM) using VDT PACE regimen and its modifications (VDT PACE-like regimens: VPLRs) outside TOTAL THERAPY trials is limited. We analyzed the outcomes of 141 patients with RRMM who received VPLRs at our center between 2006 and 2017 in an intent-to-treat analysis. Median age was 59.7 years and 66.7% of patients were male. A median of 2.2 years (range 0.02-11.4) separated diagnosis of myeloma and inititation of VPLR. High-risk cytogenetics were present in 52.4% patients. Patients received a median of 4 (range 1-14) prior therapies, including stem cell transplant (SCT) in 66.7% patients. Ninety-five (67.4%) patients received VDT PACE, 20 (14.2%) patients received VD PACE and 26 (18.4%) patients received other VPLRs. Patients received a median of 1 cycle (range 1-9) of VPLR. We observed = minimal response in 68.4%, = partial response (PR) in 54.4% and = very good PR in 10.3% patients. Median progression-free survival was 3.1 months (95% CI, 1.9-3.9) and median overall survival (OS) was 8.1 months (CI, 6.2-9.9). One-hundred and sixteen (82.3%) patients received some therapy after VPLR; 71 (61.2%) received systemic chemotherapy, while 45 (38.8%) underwent SCT. Median OS for those who received SCT after VPLR was 15.1 months (CI, 10.3-20.8). Age = 60 years (hazard ratio [HR] 2.3 [CI, 1.4-3.7]; P = 0.0008) and R-ISS III stage (HR-2.4 [CI, 1.3-4.0]; P = 0.003) predicted shorter OS in patients receiving VPLR. VPLRs are effective in heavily pre-treated RRMM. In fit patients, SCT can be used to consolidate the response to VPLR.
机译:使用VDT PACE方案复发/难治性多骨骼瘤(RRMM)的密集化化疗经验及其在总治疗试验外的改进(VDT速度等方案:VPLRS)是有限的。我们分析了141名RRMM患者的结果,在2006年至2017年期间在我们的中心接受了VPLRS,在意图分析的分析中。中位年龄为59.7岁,66.7%的患者是男性。中位数为2.2岁(范围0.02-11.4)分离骨髓瘤的诊断并启动VPLR。 52.4%的患者中存在高危细胞遗传学。患者在66.7%的患者中接受4(范围1-14)的中位数,包括干细胞移植(SCT)。九十五(67.4%)患者接受VDT速度,20名(14.2%)患者接受VD PACE和26例(18.4%)患者接受其他VPLRS。患者接受了VPLR的1个循环(范围1-9)的中位数。我们观察到& = 68.4%的最小反应,& = 54.4%的部分反应(Pr)和& = 10.3%患者中的非常好PR。中位进展生存率为3.1个月(95%CI,1.9-3.9)和中位数生存(OS)为8.1个月(CI,6.2-9.9)。一百十六(82.3%)患者在VPLR后接受了一些治疗; 71(61.2%)接受全身化疗,而45(38.8%)接受了SCT。在VPLR后收到SCT的人的中位操作系统为15.1个月(CI,10.3-20.8)。年龄& = 60岁(危险比[HR] 2.3 [CI,1.4-3.7]; p = 0.0008)和R-ISS III阶段(HR-2.4 [CI,1.3-4.0]; P = 0.003)预测较短的操作系统在接受vplr的患者中。 VPLR在大量预处理的RRMM中有效。在适合患者中,SCT可用于巩固对VPLR的响应。

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