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首页> 外文期刊>British Journal of Haematology >Phase 2 study of two sequential three-drug combinations containing bortezomib, cyclophosphamide and dexamethasone, followed by bortezomib, thalidomide and dexamethasone as frontline therapy for multiple myeloma
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Phase 2 study of two sequential three-drug combinations containing bortezomib, cyclophosphamide and dexamethasone, followed by bortezomib, thalidomide and dexamethasone as frontline therapy for multiple myeloma

机译:包含硼替佐米,环磷酰胺和地塞米松的两种连续三药组合的第二阶段研究,然后是硼替佐米,沙利度胺和地塞米松作为多发性骨髓瘤的一线治疗

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摘要

Novel sequential combination therapy for induction may improve the quality of response and therefore prolong survival in newly diagnosed multiple myeloma (MM) patients. We report results from a phase 2 study of two sequential three-drug combinations. Forty-four previously untreated, symptomatic MM patients received: bortezomib 1.3 mg/m~2 (days 1, 4, 8, 11), cyclophosphamide 300 mg/m~2 (days 1, 8), plus dexamethasone 40 mg (day of and day after bortezomib) for three 21-day cycles, followed by bortezomib 1.0 mg/m~2, dexamethasone 40 mg and thalidomide 100 mg daily for three cycles. Overall response rate for 42 evaluable patients was 95%, including 19% stringent complete response (sCR), 26% CR, and 57% >= very good partial response. Twenty-two patients have undergone stem-cell transplantation. After a median follow-up of 20.9 months, five patients have died; none was induction therapy-related. Median event-free survival (EFS) and overall survival (OS) have not been reached; estimated 1-year EFS and OS rates were 81% and 91% respectively; Both three-drug combinations were well tolerated; 82% of patients completed all six cycles. Toxicities were predictable and manageable; the most-commonly reported grade 3/4 toxicity was neuropathy (11%). This novel sequential three-drug combination therapy is effective and well-tolerated in previously untreated MM patients.
机译:用于诱导的新型序贯联合疗法可提高反应质量,从而延长新诊断的多发性骨髓瘤(MM)患者的生存期。我们报告了两个连续的三种药物组合的2期研究结果。接受过四十四例未经治疗的有症状MM患者:硼替佐米1.3 mg / m〜2(第1、4、8、11天),环磷酰胺300 mg / m〜2(第1、8天),以及地塞米松40 mg(第1天)和硼替佐米治疗后的第二天),连续三个21天周期,然后是硼替佐米1.0 mg / m〜2,地塞米松40 mg和沙利度胺100 mg,连续三个周期。 42名可评估患者的总缓解率为95%,其中包括19%的严格完全缓解(sCR),26%的CR和57%的非常好的部分缓解。 22名患者接受了干细胞移植。中位随访20.9个月后,有5例患者死亡。没有一个与诱导疗法有关。尚未达到中位数的无事件生存期(EFS)和总体生存期(OS);估计一年的EFS和OS比率分别为81%和91%;两种三药组合均具有良好的耐受性。 82%的患者完成了所有六个周期。毒性是可预测和可控制的;最常见的3/4级毒性反应是神经病(11%)。这种新颖的序贯三药联合疗法在先前未经治疗的MM患者中有效且耐受良好。

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