Non-Myeloablative Allogeneic Transplantation with Post-Transplant Cyclophosphamide after Immune Checkpoint Inhibition for Classic Hodgkin Lymphoma: A Retrospective Cohort Study

被引:26
|
作者
Paul, Suman [1 ]
Zahurak, Marianna [1 ]
Luznik, Leo [1 ]
Ambinder, Richard F. [1 ]
Fuchs, Ephraim J. [1 ]
Bolanos-Meade, Javier [1 ]
Wagner-Johnston, Nina [1 ]
Swinnen, Lode J. [1 ]
Schoch, Laura [1 ]
Varadhan, Ravi [1 ]
Jones, Richard J. [1 ]
Gladstone, Douglas E. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Bunting Blaustein Canc Res Bldg,1650 Orleans St, Baltimore, MD 21287 USA
基金
美国国家卫生研究院;
关键词
Immune checkpoint Inhibitors (ICIs); Classic Hodgkin lymphoma (cHL); Allogeneic blood or marrow transplantation (alloBMT); Post-transplantation cyclophosphamide (PTCy); Graft-versus-host-disease (GVHD); Engraftment; BONE-MARROW-TRANSPLANTATION; STEM-CELL TRANSPLANTATION; HAPLOIDENTICAL TRANSPLANTATION; BRENTUXIMAB VEDOTIN; NIVOLUMAB; EFFICACY; FAILURE; SAFETY; GVHD;
D O I
10.1016/j.bbmt.2020.06.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 prealloBMT 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. (C) 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
引用
收藏
页码:1679 / 1688
页数:10
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