Paul Suman, Zahurak Marianna, Luznik Leo, Ambinder Richard F, Fuchs Ephraim J, Bolaños-Meade Javier, Wagner-Johnston Nina, Swinnen Lode J, Schoch Laura, Varadhan Ravi, Jones Richard J, Gladstone Douglas E
Department of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Oncology, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University School of Medicine, Baltimore, Maryland..
Biol Blood Marrow Transplant. 2020 Sep;26(9):1679-1688. doi: 10.1016/j.bbmt.2020.06.012. Epub 2020 Jun 24.
: Immune checkpoint inhibitors (ICIs) are approved in relapsed classic Hodgkin lymphoma (cHL). The safety and effectiveness of allogeneic blood or marrow transplantation (alloBMT) in ICI-pretreated patients with cHL remain unclear. The aim of this study is to assess outcomes of patients with cHL receiving ICIs before alloBMT using post-transplantation cyclophosphamide (PTCy) graft-versus-host-disease (GVHD) prophylaxis. : We performed a retrospective study of relapsed/refractory patients with cHL undergoing alloBMT with PTCy at Johns Hopkins between November 2004 and September 2019. Engraftment, GVHD incidence, nonrelapse mortality, progression-free survival (PFS), and overall survival (OS) were compared between patients receiving pre-alloBMT ICI or standard salvage chemotherapy. : We identified 105 consecutive relapsed/refractory patients with cHL, of whom 37 (35.2%) received ICIs and 68 (64.7%) received chemotherapy without ICIs (no-ICI) before alloBMT. ICI and no-ICI patients experienced a 3-year estimated OS of 94% versus 78% (hazard ratio [HR], 0.35; 95% confidence interval [CI], 0.08 to 1.56; P = .17) and a 3-year estimated PFS of 90% and 65% (HR, 0.3; 95% CI, 0.09 to 1; P = .05), respectively. We observed no statically significant difference in the 12-month cumulative incidence of acute grade II to IV GVHD or in the 24-month incidence of chronic GVHD. : ICIs do not increase acute or chronic GVHD incidence compared with salvage chemotherapy. Patients with cHL receiving ICIs prior to alloBMT experienced outstanding PFS and OS. Thus, ICI therapy is safe in patients with cHL when undergoing alloBMT with PTCy and may improve post-alloBMT disease progression and survival.
免疫检查点抑制剂(ICIs)已被批准用于复发的经典型霍奇金淋巴瘤(cHL)。异基因血液或骨髓移植(alloBMT)在接受过ICI治疗的cHL患者中的安全性和有效性仍不明确。本研究的目的是评估在alloBMT前接受ICIs治疗的cHL患者采用移植后环磷酰胺(PTCy)预防移植物抗宿主病(GVHD)的预后情况。我们对2004年11月至2019年9月期间在约翰·霍普金斯医院接受alloBMT并使用PTCy的复发/难治性cHL患者进行了一项回顾性研究。比较了接受alloBMT前ICI治疗的患者与接受标准挽救化疗的患者的植入情况、GVHD发生率、非复发死亡率、无进展生存期(PFS)和总生存期(OS)。我们确定了105例连续的复发/难治性cHL患者,其中37例(35.2%)在alloBMT前接受了ICIs治疗,68例(64.7%)接受了不使用ICIs的化疗(无ICI)。ICI组和无ICI组患者的3年估计OS分别为94%和78%(风险比[HR],0.35;95%置信区间[CI],0.08至1.56;P = 0.17),3年估计PFS分别为90%和65%(HR,0.3;95%CI,0.09至1;P = 0.05)。我们观察到急性II至IV级GVHD的12个月累积发生率或慢性GVHD的24个月发生率没有统计学上的显著差异。与挽救化疗相比,ICIs不会增加急性或慢性GVHD的发生率。在alloBMT前接受ICIs治疗的cHL患者具有出色的PFS和OS。因此,cHL患者在接受alloBMT并使用PTCy时,ICI治疗是安全的,并且可能改善alloBMT后的疾病进展和生存期。