Merryman Reid W, Edwin Natasha, Redd Robert, Bsat Jad, Chase Matthew, LaCasce Ann, Freedman Arnold, Jacobson Caron, Fisher David, Ng Samuel, Crombie Jennifer, Kim Austin, Odejide Oreofe, Davids Matthew S, Brown Jennifer R, Jacene Heather, Cashen Amanda, Bartlett Nancy L, Mehta-Shah Neha, Ghobadi Armin, Kahl Brad, Joyce Robin, Armand Philippe, Jacobsen Eric
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Division of Medical Oncology, Washington University School of Medicine, St. Louis, MO.
Blood Adv. 2020 Mar 10;4(5):858-867. doi: 10.1182/bloodadvances.2019001355.
The addition of high-dose cytarabine to rituximab/bendamustine (RB) induction could improve outcomes for transplant-eligible patients with mantle cell lymphoma (MCL). We conducted a pooled analysis of 2 phase 2 trials and an off-trial cohort each testing 3 cycles of RB and 3 cycles of rituximab/high-dose cytarabine (RC) followed by autologous stem cell transplantation (ASCT) among untreated, transplant-eligible patients with MCL. Dana-Farber Cancer Institute (DFCI) and Washington University in St. Louis (WUSTL) led separate phase 2 trials testing sequential and alternating cycles of RB/RC, respectively. Patients treated at DFCI with sequential RB/RC off trial were retrospectively identified. Minimal residual disease (MRD) was assessed in the DFCI trial. A total of 88 patients (23 DFCI trial, 18 WUSTL trial, and 47 off trial) received RB/RC; 92% of patients completed induction, and 84% underwent planned consolidative ASCT. Grade 3 or 4 adverse events among trial patients included lymphopenia (88%), thrombocytopenia (85%), neutropenia (83%), and febrile neutropenia (15%). There were no treatment-related deaths during induction and 2 following ASCT. Among 87 response-evaluable patients, the end-of-induction overall and complete response rates were 97% and 90%, respectively. After a median follow-up of 33 months, 3-year progression-free survival and overall survival were 83% and 92%, respectively. Patients undergoing MRD testing experienced prolonged MRD negativity after ASCT with emergence of MRD occurring in only 1 patient who subsequently relapsed. RB/RC followed by ASCT achieves high rates of durable remissions in transplant-eligible patients with MCL. These trials were registered at www.clinicaltrials.gov as #NCT01661881 (DFCI trial) and #NCT02728531 (WUSTL trial).
在利妥昔单抗/苯达莫司汀(RB)诱导方案中添加大剂量阿糖胞苷可改善适合移植的套细胞淋巴瘤(MCL)患者的预后。我们对2项2期试验和1个非试验队列进行了汇总分析,每项研究均在未接受治疗、适合移植的MCL患者中测试3个周期的RB和3个周期的利妥昔单抗/大剂量阿糖胞苷(RC),随后进行自体干细胞移植(ASCT)。达纳-法伯癌症研究所(DFCI)和圣路易斯华盛顿大学(WUSTL)分别牵头进行了2期试验,测试RB/RC的序贯和交替周期。对在DFCI接受序贯RB/RC非试验治疗的患者进行了回顾性鉴定。在DFCI试验中评估了微小残留病(MRD)。共有88例患者(23例来自DFCI试验,18例来自WUSTL试验,47例来自非试验队列)接受了RB/RC治疗;92%的患者完成了诱导治疗,84%的患者接受了计划中的巩固性ASCT。试验患者中3级或4级不良事件包括淋巴细胞减少(88%)、血小板减少(85%)、中性粒细胞减少(83%)和发热性中性粒细胞减少(15%)。诱导治疗期间无治疗相关死亡,ASCT后有2例死亡。在87例可评估缓解的患者中,诱导结束时的总缓解率和完全缓解率分别为97%和90%。中位随访33个月后,3年无进展生存率和总生存率分别为83%和92%。接受MRD检测的患者在ASCT后经历了较长时间的MRD阴性,仅1例患者出现MRD,随后复发。RB/RC序贯ASCT可使适合移植的MCL患者获得较高的持久缓解率。这些试验已在www.clinicaltrials.gov上注册,注册号分别为#NCT01661881(DFCI试验)和#NCT02728531(WUSTL试验)。