Stritch School of Medicine, Loyola University Chicago, Maywood, IL, USA.
Division of Hematology Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Leuk Lymphoma. 2020 Dec;61(14):3484-3492. doi: 10.1080/10428194.2020.1811275. Epub 2020 Aug 31.
Melphalan at a dose of 200 mg/m (MEL200) remains the standard high dose therapy before autologous stem cell transplantation (ASCT) for multiple myeloma (MM). Intensifying the high dose regimen has shown promising results. We report here 7-year follow up of our novel high dose regimen of busulfan and melphalan followed by bortezomib (BuMelVel). Forty-three MM patients received BuMelVel high dose therapy with pharmacokinetic adjusted busulfan. Outcomes were compared to a matched control cohort from the CIBMTR database ( = 162) receiving MEL200. The primary endpoint was progression free survival. Five year PFS was 47% v 30% (95% CI; 32-62) in favor or the BuMelVel group (95% CI; 23-37) ( = 0.05). In multivariate analysis for PFS, BuMelVel (HR 0.65; 95% CI 0.44-0.97)( = 0.036) was predictive. Similar to recent reports of double alkylator therapy, although depth of response was similar between the BuMelVel group and MEL200, the BUMELVEL group experienced an improved PFS.
美法仑 200mg/m2(MEL200)仍然是多发性骨髓瘤(MM)患者自体干细胞移植(ASCT)前的标准大剂量治疗方案。强化大剂量方案已显示出良好的效果。我们在此报告我们的新型硼替佐米联合大剂量美法仑和马法兰(BuMelVel)方案的 7 年随访结果。43 例 MM 患者接受了美法仑 200mg/m2 方案治疗。与接受 MEL200 方案的 CIBMTR 数据库中的匹配对照队列(n=162)相比,BuMelVel 组患者接受了基于药代动力学调整的马法兰治疗。主要终点是无进展生存。BuMelVel 组 5 年 PFS 为 47%,而 MEL200 组为 30%(95%CI:32-62)(95%CI:23-37)(=0.05)。多因素分析显示,BuMelVel(HR 0.65;95%CI 0.44-0.97)(=0.036)是 PFS 的预测因素。与最近的双烷化剂治疗报告类似,尽管 BuMelVel 组与 MEL200 组的缓解深度相似,但 BuMelVel 组的 PFS 得到了改善。