Hur Joon Young, Yoon Sang Eun, Kim Seok Jin, Kim Won Seog
Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Division of Hematology and Oncology, Department of Internal Medicine, Hanyang University Guri Hospital, Guri, Korea.
Blood Res. 2020 Jun 30;55(2):85-90. doi: 10.5045/br.2020.2020014.
Immune checkpoint inhibitors have demonstrated efficacy in the treatment of classical Hodgkin's lymphoma (cHL). We analyzed the efficacy and safety of pembrolizumab or nivolumab in patients with pretreated cHL.
Clinical data from the cancer chemotherapy registry of Samsung Medical Center were retrospectively analyzed to study patients with cHL treated with pembrolizumab or nivolumab between Oct 2015 and Dec 2018.
Of the 20 patients, seven (35%) were enrolled in the study after a relapse following autologous hematopoietic stem cell transplantation (ASCT) and 12 (60%) after a relapse following receipt of brentuximab vedotin (BV). Sixteen (80%) patients received pembrolizumab, and four (20%) patients received nivolumab. The complete remission rate was 45% (9/20), and 30% (6/20) of patients achieved partial remission, for an overall response rate (RR) of 75% [15/20; 95% confidence interval (CI), 34.7‒93.3]. With a median follow-up duration of 14 months, the median PFS was 18 months (95% CI, 2.4‒33.5 mo), and the median OS was 36 months [95% CI, 36-not applicable (NA) mo]. Pembrolizumab and nivolumab were generally well tolerated.
In this study, pembrolizumab and nivolumab both demonstrated clinical efficacy and tolerability in patients with cHL who failed previous chemotherapy or ASCT.
免疫检查点抑制剂已在经典型霍奇金淋巴瘤(cHL)的治疗中显示出疗效。我们分析了帕博利珠单抗或纳武利尤单抗在经治cHL患者中的疗效和安全性。
回顾性分析三星医疗中心癌症化疗登记处的临床数据,以研究2015年10月至2018年12月期间接受帕博利珠单抗或纳武利尤单抗治疗的cHL患者。
20例患者中,7例(35%)在自体造血干细胞移植(ASCT)后复发,12例(60%)在接受维布妥昔单抗(BV)治疗后复发。16例(80%)患者接受了帕博利珠单抗治疗,4例(20%)患者接受了纳武利尤单抗治疗。完全缓解率为45%(9/20),30%(6/20)的患者达到部分缓解,总缓解率(RR)为75%[15/20;95%置信区间(CI),34.7‒93.3]。中位随访时间为14个月,中位无进展生存期(PFS)为18个月(95%CI,2.4‒33.5个月),中位总生存期(OS)为36个月[95%CI,36-不可用(NA)个月]。帕博利珠单抗和纳武利尤单抗总体耐受性良好。
在本研究中,帕博利珠单抗和纳武利尤单抗在既往化疗或ASCT失败的cHL患者中均显示出临床疗效和耐受性。