Calcineurin and mTOR Inhibitor-Free Post-Transplantation Cyclophosphamide and Bortezomib Combination for Graft-versus-Host Disease Prevention after Peripheral Blood Allogeneic Hematopoietic Stem Cell Transplantation: A Phase I/II Study

被引:13
作者
Al-Homsi, A. Samer [1 ,2 ,4 ]
Cole, Kelli [1 ]
Muilenburg, Marlee [1 ]
Goodyke, Austin [1 ]
Abidi, Muneer [1 ,2 ]
Duffner, Ulrich [1 ,2 ]
Williams, Stephanie [1 ,2 ]
Parker, Jessica [3 ]
Abdel-Mageed, Aly [1 ,2 ]
机构
[1] Spectrum Hlth, Blood & Marrow Transplantat Program, 145 Michigan St NE,Suite 5200, Grand Rapids, MI 49503 USA
[2] Michigan State Univ, Coll Human Med, Grand Rapids, MI USA
[3] Spectrum Hlth, Off Res Adm, Grand Rapids, MI USA
[4] New York Univ Hosp, Blood & Marrow Transplantat, Ambulatory Care Bldg,240 E 38th St, New York, NY 10016 USA
关键词
Allogeneic hematopoietic stem cell transplantation; Graft-versus-host disease prophylaxis; Post-transplantation cyclophosphamide; Bortezomib; UNRELATED DONOR TRANSPLANTATION; REGULATORY T-CELLS; II TRIAL; PROPHYLAXIS; GVHD; PRESERVES; SIROLIMUS; DEPLETION; ANTIGEN; AGENT;
D O I
10.1016/j.bbmt.2017.05.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Graft-versus-host disease (GVHD) hampers the utility of allogeneic hematopoietic stem cell transplantation (AHSCT). The purpose of this study was to determine the feasibility, safety, and efficacy of a novel combination of post-transplantation cyclophosphamide (PTC) and bortezomib for the prevention of GVHD. Patients undergoing peripheral blood AHSCT for hematological malignancies after reduced-intensity conditioning with grafts from HLA-matched related or unrelated donors were enrolled in a phase clinical trial. Patients received a fixed dose of PTC and an increasing dose of bortezomib in 3 cohorts, from.7 to 1 and then to 1.3 mg/m(2), administered 6 hours after graft infusion and 72 hours thereafter, during phase I. The study was then extended at the higher dose in phase II for a total of 28 patients. No graft failure and no unexpected grade >= 3nonhematologic toxicities were encountered. The median times to neutrophil and platelet engraftment were 16 and 27 days, respectively. Day +100 treatment-related mortality was 3.6% (95% confidence interval [CI],.2% to 15.7%). The cumulative incidences of grades II to IV and grades III and IV acute GVHD were 35.9% (95% CI, 18.6% to 53.6%) and 11.7% (95% CI, 2.8% to 27.5%), respectively. The incidence of chronic GVHD was 27% (95% CI, 11.4% to 45.3%). Progression-free survival, overall survival, and GVHD and relapse-free survival rates were 50% (95% CI, 30.6% to 66.6%), 50.8% (95% CI, 30.1% to 68.2%), and 37.7% (95% CI, 20.1% to 55.3%), respectively. Immune reconstitution, measured by CD3, CD4, and CD8 recovery, was prompt. The combination of PTC and bortezomib for the prevention of GVHD is feasible, safe, and yields promising results. The combination warrants further examination in a multi-institutional trial. (C) 2017 American Society for Blood and Marrow Transplantation:
引用
收藏
页码:1651 / 1657
页数:7
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