Department of Hematology, Tangdu Hospital, Fourth Military Medical University (Air Force Medical University), Xi'an, China.
Hematol Oncol. 2023 Aug;41(3):396-406. doi: 10.1002/hon.3116. Epub 2022 Dec 30.
Extranodal natural killer/T cell lymphoma (ENKTL) patients typically face a grim prognosis after relapse or progression following asparaginase-based chemotherapy. Currently, programmed cell death protein-1 (PD-1) immune checkpoint blockade has shown promising efficacy as an optimal regimen for relapsed or refractory ENKTL (rrENKTL) patients. This study retrospectively investigated the efficacy, safety, and factors influencing the survival of 26 rrENKTL patients who underwent monoclonal antibody treatment using PD-1 (Sintilimab or Camrelizumab) alone or combined with chemotherapy from January 2018 to February 2022. The disease control rate was 73.1%, and the objective response rate was 50.0%. 15.4% of the patients achieved complete remission, and 34.6% achieved partial remission (PR). After a median follow-up of 12 (range 3-47) months, the median progression-free survival (PFS) and overall survival (OS) were 6.5 and 13.3 months. The 1-year PFS and OS rate were 23.1% and 53.8%. 96.2% of patients experienced at least one adverse event and 26.9% experienced grade 1-2 immune-related adverse events. PD-1 inhibitor improved rrENKTL patient survival, and the AEs were controlled. We also observed that the prognostic index for NK cell lymphoma including Epstein-Barr virus (EBV) (PINK-E) and the nomogram-revised risk indexz for ENKTL patients could help identify a potentially unfavorable prognosis in this era of immunotherapy. More attention should be paid to the presence of EBV after anti-PD-1 immunotherapy, as it more accurately indicates a poor prognosis.
结外自然杀伤/T 细胞淋巴瘤(ENKTL)患者在基于门冬酰胺酶的化疗后复发或进展后通常预后不良。目前,程序性死亡蛋白-1(PD-1)免疫检查点阻断已显示出作为复发或难治性 ENKTL(rrENKTL)患者的最佳方案的有希望的疗效。本研究回顾性调查了 26 例 rrENKTL 患者在 2018 年 1 月至 2022 年 2 月期间单独使用 PD-1(信迪利单抗或卡瑞利珠单抗)或联合化疗进行单克隆抗体治疗的疗效、安全性和影响生存的因素。疾病控制率为 73.1%,客观缓解率为 50.0%。15.4%的患者达到完全缓解,34.6%达到部分缓解(PR)。中位随访 12 个月(范围 3-47 个月)后,中位无进展生存期(PFS)和总生存期(OS)分别为 6.5 个月和 13.3 个月。1 年 PFS 和 OS 率分别为 23.1%和 53.8%。96.2%的患者至少发生一次不良事件,26.9%的患者发生 1-2 级免疫相关不良事件。PD-1 抑制剂改善了 rrENKTL 患者的生存,并且可以控制 AE。我们还观察到,包括 EBV(PINK-E)在内的 NK 细胞淋巴瘤预后指数和 ENKTL 患者的修正风险指数预测模型有助于识别在免疫治疗时代可能不利的预后。在抗 PD-1 免疫治疗后应更加关注 EBV 的存在,因为它更准确地提示预后不良。