Single Antigen-Mismatched Unrelated Hematopoietic Stem Cell Transplantation Using High-Dose Post-Transplantation Cyclophosphamide Is a Suitable Alternative for Patients Lacking HLA-Matched Donors

被引:50
作者
Sofia Jorge, Ana [1 ]
Suarez-Lledo, Maria [1 ]
Pereira, Arturo [2 ]
Gutierrez, Gonzalo [1 ,3 ,4 ]
Fernandez-Aviles, Francesc [1 ,3 ,4 ]
Rosinol, Laura [1 ,3 ,4 ]
Llobet, Noemi [1 ]
Solano, Teresa [1 ]
Urbano-Ispizua, Alvaro [1 ,3 ,4 ]
Rovira, Montserrat [1 ,3 ,4 ]
Martinez, Carmen [1 ,3 ,4 ]
机构
[1] Hosp Clin Barcelona, Inst Hematol & Oncol, Hematol Dept, Hematopoiet Stem Cell Transplantat Unit, Barcelona, Spain
[2] Hosp Clin Barcelona, Hemotherapy & Hemostasis Dept, Barcelona, Spain
[3] August Pi & Sunyer Biomed Res Inst IDIBAPS, Barcelona, Spain
[4] Hosp Clin Barcelona, Josep Carreras Leukaemia Res Fdn, Barcelona, Spain
关键词
HLA-mismatched transplantation; Post-transplantation cyclophosphamide; Unrelated donor; Graft-versus-host disease; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; HAPLOIDENTICAL TRANSPLANTATION; ANTITHYMOCYTE GLOBULIN; IDENTICAL SIBLINGS; HIGH-RISK; CLASS-I; HEMATOLOGIC MALIGNANCIES; CONDITIONING REGIMEN; ACUTE-LEUKEMIA;
D O I
10.1016/j.bbmt.2018.01.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The optimal prophylaxis regimen for graft-versus-host disease (GVHD) in the setting of mismatched unrelated donor (MMUD) allogeneic hematopoietic stem cell transplantation (alloHSCT) is not defined. The use of high-dose post-transplant cyclophosphamide (PTCy) in haploidentical transplantation has proven feasible and effective in overcoming the negative impact of HLA disparity on survival. We hypothesized that PTCy could also be effective in the setting of MMUD transplantation. We retrospectively analyzed 86 consecutive adult recipients of alloHSCT in our institution, comparing 2 contemporaneous groups: PTCy MMUD (n = 26) versus matched unrelated donor (MUD) (n = 60). Graft source was primarily peripheral blood (92%). All PTCy MMUD were HLA 7/8 (differences in HLA class I loci in 92% of patients) and received PTCy plus tacrolimus +/- mofetil mycophenolate as GVHD prophylaxis. No differences were observed between PTCy MMUD and MUD in the 100-day cumulative incidence of acute GVHD grades II to IVq31% versus 22%, respectively; P= .59) and III to IV (8% versus 10%, P=.67). , There was a trend for a lower incidence of moderate to severe chronic GVHD at 1 year after PTCy MMUD in Comparison with MUD (22% versus 41%, P = .098). No differences between PTCy MMUD and MUD were foundregarding nonrelapse mortality (25% versus 18%, P= .52) or relapse rate (11% versus 19%, P = .18). Progression-free survival and overall survival at 2 years were similar in both cohorts (67% versus 54% [HR, .84; 95%, CI, .38 to 1.88; P= .68] and 72% versus 57% [HR, .71; 95% CI, .31 to 1.67; P = .44], respectively). The 2-year cumulative incidence of survival free of moderate to severe chronic GVHD and relapse tended to be higher in the PTCy MMUD group (47% versus 24%; HR, .60; 95% CI, .31 to 1.14; P = .12). We conclude that HLA 7/8, MMUD transplantation using PTCy plus tacrolimus is a suitable alternative for those patients who lack a MUD. (C) 2018 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:1196 / 1202
页数:7
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