Fludarabine and Total-Body Irradiation Conditioning before Ablative Haploidentical Transplantation: Long-Term Safety and Efficacy

被引:17
作者
Solomon, Scott R. [1 ]
Solh, Melhem [1 ]
Zhang, Xu [2 ]
Morris, Lawrence E. [1 ]
Holland, H. Kent [1 ]
Bashey, Asad [1 ]
机构
[1] Northside Hosp, Blood & Marrow Transplant Program, Atlanta, GA USA
[2] Univ Texas Houston, Sch Publ Hlth, Houston, TX USA
关键词
Haploidentical; Post-transplant cyclophosphamide; Myeloablative; Total body; Irradiation; GRFS; CGRFS; BONE-MARROW-TRANSPLANTATION; STEM-CELL TRANSPLANTATION; VERSUS-HOST-DISEASE; RELAPSE-FREE SURVIVAL; HEMATOLOGIC MALIGNANCIES; POSTTRANSPLANTATION CYCLOPHOSPHAMIDE; DONOR TRANSPLANTATION; BLOOD; OUTCOMES; TRIALS;
D O I
10.1016/j.bbmt.2019.06.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although myeloablative conditioning (MAC) before haploidentical donor transplant (HIDT) with post-transplant cyclophosphamide is being increasingly used, the optimal preparative regimen remains unclear. In our initial trial, the feasibility of HIDT following a MAC preparative regimen using fludarabine and 12 Gy of total-body irradiation was demonstrated in 30 patients. We now present long-term outcome results, including an additional 52 patients, now with 47 months (16 to 96) median follow-up. Median patient age was 42 (19 to 61) years. The most common diagnoses were acute myelogenous leukemia (51%) and acute lymphoblastic leukemia (33%), and 39% had a high/very high disease risk index (DRI). Engraftment was universal with no cases of primary or secondary graft failure. Grade 3 to 4 acute graft-versus-host disease (GVHD) and moderate to severe chronic GVHD occurred in 17% and 23%, respectively. Nonrelapse mortality (NRM) was 7% at 1 year and 13% at 4 years. Estimated 4-year overall survival (OS), disease-free survival, and cumulative incidence of relapse (CIR) were 67%, 60%, and 27%, respectively. CIR was significantly higher in patients with high/very high-versus low/intermediate-risk DRI (38% versus 20%, P=.032), which led to inferior 4-year OS (50% versus 77%, P=.001). Median time to systemic immunosuppressive therapy (IST) discontinuation was 7.8 months, with 84% of patients off 1ST at 2 years post-transplant. Current GHVD-free, relapse-free survival (CGRFS) at 2, 3, and 4 years was 60%, 57%, and 60%, respectively. This approach to MAC HIDT results in universal engraftment; low rates of NRM, infection, and clinically significant GVHD; and relatively rapid 1ST discontinuation, resulting in high rates of CGRFS and survival. (C) 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
引用
收藏
页码:2211 / 2216
页数:6
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