Mount Sinai Hospital, New York, NY.
Simon Cancer Center, Indiana University, Indianapolis, IN.
Blood Adv. 2018 Jul 10;2(13):1608-1615. doi: 10.1182/bloodadvances.2018017186.
Autologous stem cell transplantation (ASCT) followed by lenalidomide maintenance therapy is the standard of care for transplant-eligible patients with newly diagnosed multiple myeloma (NDMM). Clinical trials show progression-free survival (PFS) benefits, with some studies (Cancer and Leukemia Group [CALGB] trial and meta-analysis) also showing overall survival (OS) benefits, but applicability to real-world clinical settings is unclear. Using data from Connect MM, the largest US-based observational registry of NDMM patients, we analyzed effects of maintenance therapy on long-term outcomes in 1450 treated patients enrolled from 2009 to 2011. Patients who received induction therapy and ASCT (n = 432) were analyzed from 100 days post-ASCT (data cut 7 January 2016): 267 received maintenance (80% lenalidomide-based [of whom 88% received lenalidomide monotherapy]); 165 did not. Lenalidomide maintenance improved median PFS and 3-year PFS rate vs no maintenance (50.3 vs 30.8 months [hazard ratio (HR), 0.62; 95% confidence interval (CI), 0.46-0.82; < .001] and 56% vs 42%, respectively). Improvements in median OS and 3-year OS rate were associated with lenalidomide maintenance vs no maintenance (not reached in either group [HR, 0.54; 95% CI, 0.36-0.83; = .005] and 85% vs 70%, respectively). Five hematologic serious adverse events were reported with lenalidomide maintenance (pancytopenia [n = 2], febrile neutropenia, anemia, and thrombocytopenia [n = 1 each]) and 1 with no maintenance (thrombocytopenia). Second primary malignancies occurred at rates of 1.38 and 2.19 events per patient-year in lenalidomide maintenance and no maintenance groups, respectively. Survival benefits associated with lenalidomide maintenance previously demonstrated in clinical trials were observed in this community-based Connect MM Registry.
自体干细胞移植(ASCT)后接受来那度胺维持治疗是适合移植的新发多发性骨髓瘤(NDMM)患者的标准治疗方法。临床试验显示无进展生存期(PFS)获益,一些研究(癌症和白血病小组[CALGB]试验和荟萃分析)也显示总生存期(OS)获益,但对真实临床环境的适用性尚不清楚。利用来自 Connect MM 的数据,这是美国最大的 NDMM 患者观察性登记处,我们分析了维持治疗对 1450 名于 2009 年至 2011 年入组的接受治疗患者的长期结局的影响。从 ASCT 后 100 天(数据截止日期为 2016 年 1 月 7 日)对接受诱导治疗和 ASCT 的患者(n = 432)进行分析:267 名患者接受维持治疗(80%基于来那度胺[其中 88%接受来那度胺单药治疗]);165 名患者未接受维持治疗。与未接受维持治疗相比,来那度胺维持治疗改善了中位 PFS 和 3 年 PFS 率(50.3 个月与 30.8 个月[风险比(HR),0.62;95%置信区间(CI),0.46-0.82;<.001]和 56%与 42%)。与未接受维持治疗相比,中位 OS 和 3 年 OS 率的改善与来那度胺维持治疗相关(两组均未达到终点[HR,0.54;95%CI,0.36-0.83; =.005]和 85%与 70%)。来那度胺维持治疗报告了 5 例血液学严重不良事件(全血细胞减少症[n = 2]、发热性中性粒细胞减少症、贫血和血小板减少症[各 1 例])和 1 例未接受维持治疗的事件(血小板减少症)。来那度胺维持治疗组和未接受维持治疗组的第二原发恶性肿瘤发生率分别为每患者年 1.38 次和 2.19 次。在这项基于社区的 Connect MM 登记研究中观察到了来那度胺维持治疗在临床试验中先前显示的生存获益。