Division of Hematology and Medical Oncology, Perlmutter Cancer Center at NYU Langone Health, New York University School of Medicine & Langone Medical Center, New York, NY, USA.
Department of Medical Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
Br J Haematol. 2020 Oct;191(1):44-51. doi: 10.1111/bjh.16756. Epub 2020 May 19.
Patients with relapsed/refractory (R/R) non-Hodgkin lymphoma (NHL) have limited options for salvage, and checkpoint blockade therapy (CBT) has little efficacy. Usage in solid malignancies suggests that CBT sensitises tumours to subsequent chemotherapy. We performed the first analysis of CBT on subsequent NHL treatment. Seventeen North American centres retrospectively queried records. The primary aim was to evaluate the overall response rate (ORR) to post-CBT treatment. Secondary aims included progression-free survival (PFS), duration of response (DOR) and overall survival (OS). Fifty-nine patients (68% aggressive NHL, 69% advanced disease) were included. Patients received a median of three therapies before CBT. Fifty-three (90%) discontinued CBT due to progression. Post-CBT regimens included chemotherapy (49%), targeted therapy (30%), clinical trial (17%), transplant conditioning (2%) and chimeric antigen receptor T cell (CAR-T) therapy (2%). The ORR to post-CBT treatment was 51%, with median PFS of 6·1 months. In patients with at least stable disease (SD) to post-CBT, the median DOR was significantly longer than to pre-CBT (310 vs. 79 days, P = 0·005) suggesting sensitisation. Nineteen patients were transplanted after post-CBT therapy. Median overall survival was not reached, nor affected by regimen. Prospective trials are warranted, as this may offer R/R NHL patients a novel therapeutic approach.
复发/难治性 (R/R) 非霍奇金淋巴瘤 (NHL) 患者的挽救治疗选择有限,而检查点阻断治疗 (CBT) 的疗效有限。在实体恶性肿瘤中的应用表明,CBT 可使肿瘤对后续化疗敏感。我们首次对 NHL 后续治疗中 CBT 的应用进行了分析。17 个北美中心回顾性查询了记录。主要目的是评估 CBT 后治疗的总缓解率 (ORR)。次要目的包括无进展生存期 (PFS)、缓解持续时间 (DOR) 和总生存期 (OS)。共纳入 59 例患者(68%侵袭性 NHL,69%晚期疾病)。患者在 CBT 前接受了中位数为 3 种治疗。由于进展,53 例(90%)停止了 CBT。CBT 后的方案包括化疗(49%)、靶向治疗(30%)、临床试验(17%)、移植预处理(2%)和嵌合抗原受体 T 细胞 (CAR-T) 治疗(2%)。CBT 后治疗的 ORR 为 51%,中位 PFS 为 6.1 个月。在至少有疾病稳定 (SD) 至 CBT 后治疗的患者中,DOR 明显长于 CBT 前(310 天 vs. 79 天,P=0.005),提示敏感性。19 例患者在 CBT 后进行了移植。中位总生存期未达到,也不受方案影响。需要前瞻性试验,因为这可能为 R/R NHL 患者提供一种新的治疗方法。