Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Division of Hematology/Oncology, Massachusetts General Hospital, Boston, MA.
Blood. 2019 Jul 4;134(1):22-29. doi: 10.1182/blood.2019000215. Epub 2019 Apr 5.
Autologous stem cell transplantation (ASCT) remains the standard of care for patients with relapsed/refractory (RR) classical Hodgkin lymphoma (cHL) who respond to salvage chemotherapy. However, relapse after ASCT remains a frequent cause of treatment failure, with poor subsequent prognosis. Because cHL is uniquely vulnerable to programmed cell death-1 (PD-1) blockade, PD-1 blockade given as consolidation after ASCT could improve ASCT outcomes. We therefore conducted a multicohort phase 2 study of pembrolizumab in patients with RR cHL after ASCT, hypothesizing that it would improve the progression-free survival (PFS) at 18 months after ASCT (primary end point) from 60% to 80%. Pembrolizumab was administered at 200 mg IV every 3 weeks for up to 8 cycles, starting within 21 days of post-ASCT discharge. Thirty patients were treated on this study. The median age was 33 years, and 90% were high-risk by clinical criteria. Seventy-seven percent completed all 8 cycles. Toxicity was manageable, with 30% of patients experiencing at least 1 grade 3 or higher adverse event (AE), and 40% at least 1 grade 2 or higher immune-related AE. Two patients were lost to follow-up in complete remission at 12 months. The PFS at 18 months for the 28 evaluable patients was 82%, meeting the primary end point. The 18-month overall survival was 100%. In conclusion, pembrolizumab was successfully administered as post-ASCT consolidation in patients with RR cHL, and resulted in a promising PFS in a high-risk patient cohort, supporting the testing of this strategy in a randomized trial. This trial was registered at www.clinicaltrials.gov as #NCT02362997.
自体干细胞移植(ASCT)仍然是对接受挽救性化疗后缓解/复发(RR)经典霍奇金淋巴瘤(cHL)患者的标准治疗方法。然而,ASCT 后复发仍然是治疗失败的常见原因,预后较差。由于 cHL 特别容易受到程序性细胞死亡-1(PD-1)阻断的影响,因此 ASCT 后进行 PD-1 阻断作为巩固治疗可能会改善 ASCT 结果。因此,我们进行了一项多队列 2 期研究,评估了 ASCT 后 RR cHL 患者接受 pembrolizumab 的疗效,假设它将改善 ASCT 后 18 个月的无进展生存期(PFS)(主要终点),从 60%提高到 80%。pembrolizumab 以 200mg IV 每 3 周给药,最多 8 个周期,从 ASCT 出院后 21 天内开始。本研究共治疗了 30 例患者。中位年龄为 33 岁,90%的患者按临床标准属于高危人群。77%的患者完成了所有 8 个周期的治疗。毒性可管理,30%的患者发生至少 1 级 3 或更高级别的不良事件(AE),40%发生至少 1 级 2 或更高级别的免疫相关 AE。2 例患者在完全缓解后 12 个月失访。28 例可评估患者的 18 个月 PFS 为 82%,达到主要终点。18 个月的总生存率为 100%。总之,pembrolizumab 成功地作为 RR cHL 患者 ASCT 后的巩固治疗药物,在高危患者队列中取得了有希望的 PFS,支持在随机试验中进一步测试该策略。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT02362997。