PTCy, abatacept, and a short course of tacrolimus for GVHD prevention after haploidentical transplantation

被引:23
作者
Al-Homsi, A. Samer [1 ,4 ]
Cirrone, Frank [1 ]
Wo, Stephanie [1 ]
Cole, Kelli [1 ]
Suarez-Londono, Andres [1 ]
Gardner, Sharon L. [1 ]
Hsu, Jingmei [1 ]
Stocker, Kelsey [1 ]
Bruno, Benedetto [2 ]
Goldberg, Judith D. [3 ]
Levinson, Benjamin A. [3 ]
Abdul-Hay, Maher [1 ]
机构
[1] NYU Langone Hlth, Blood & Marrow Transplantat & Cellular Therapy, New York, NY USA
[2] Univ Torino, Div Hematol, Turin, Italy
[3] NYU, Dept Populat Hlth, Div Biostat, Grossman Sch Med, New York, NY USA
[4] New York Univ Grossman Sch Med, New York Univ Langone Hlth, Transplant & Cellular Therapy, 610 2nd Ave, New York, NY 10016 USA
关键词
BONE-MARROW-TRANSPLANTATION; UMBILICAL-CORD BLOOD; PHASE-II TRIAL; POSTTRANSPLANT CYCLOPHOSPHAMIDE; COSTIMULATION BLOCKADE; STEM-CELLS; DONORS;
D O I
10.1182/bloodadvances.2023010545
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reducing the incidence of graft-versus-host disease (GVHD) after haploidentical hematopoietic stem cell transplantation (HSCT) is warranted. Posttransplant cyclophosphamide (PTCy) is the main agent used for GVHD prevention in this setting. It remains unknown whether costimulation blockade can be safely combined with PTCy and enhance its efficacy. We performed a phase 1b-2 clinical trial to examine the combination of PTCy, abatacept, and a short course of tacrolimus (CAST) after peripheral blood haploidentical HSCT. The primary end point was the incidence of grades 2-4 acute GVHD by day +120. The study enrolled 46 patients with a median age of 60 years (range, 18-74 years). The cumulative incidences of grades 2-4 and 3 or 4 acute GVHD were 17.4% (95% confidence interval [CI], 9.2-32.9) and 4.4% (95% CI, 1.1-17.1), respectively. With a median follow-up of 15.3 months, the cumulative incidence of 1-year treatment-related mortality was 4.4% (95% CI, 1.1-17.1). The estimated 1-year moderate-to-severe chronic GVHD rate, relapse rate, progression-free survival, overall survival, and GVHD- and relapse-free survival were 75.9-97.2), and 66.1% (95% CI, 53.4-81.8), respectively. Toxicities were similar to those expected in patients receiving haploidentical HSCT. This clinical trial showed that the CAST regimen is safe and effective in reducing the rate of grades 2-4 acute GVHD after haploidentical peripheral blood HSCT. This trial was registered at www.clinicaltrials.gov as #NCT04503616.
引用
收藏
页码:3604 / 3611
页数:8
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