Influence of conditioning regimen intensity on outcomes post-allogeneic hematopoietic cell transplantation for acute myeloid leukemia in complete morphological remission

被引:2
|
作者
Moya, Tommy Alfaro [1 ]
Mattsson, Jonas [1 ]
Remberger, Mats [1 ]
Lipton, Jeffrey H. [1 ]
Kim, Dennis D. [1 ]
Viswabandya, Auro [1 ]
Kumar, Rajat [1 ]
Lam, Wilson [1 ]
Law, Arjun D. [1 ]
Gerbitz, Armin [1 ]
Pasic, Ivan [1 ]
Novitzky-Basso, Igor [1 ]
Michelis, Fotios V. [1 ,2 ]
机构
[1] Princess Margaret Canc Ctr, Hans Messner Allogene Transplant Program, Toronto, ON, Canada
[2] Univ Toronto, Princess Margaret Canc Ctr, Dept Med, Hans Messner Allogene Transplant Program, 610 Univ Ave, Toronto, ON M5G 2M9, Canada
关键词
acute myeloid leukemia; allogeneic stem cell transplantation; conditioning regimen intensity; MAC; outcomes; propensity-matched analysis; RIC; REDUCED-INTENSITY; MYELODYSPLASTIC SYNDROME; BLOOD; MARROW;
D O I
10.1111/ejh.14041
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The literature comparing outcomes between myeloablative (MAC) and reduced intensity conditioning (RIC) for acute myeloid leukemia (AML) is conflicting. Methods: We retrospectively analyzed 451 patients who underwent allogenic hematopoietic cell transplantation (alloHCT) for AML in complete remission (CR) with either RIC (n = 331) or MAC (n = 120) with the use of dual T-cell depletion as graft-versus-host disease (GVHD) prophylaxis. Results: Univariate analysis demonstrated nonrelapse mortality (NRM) at 2 years was 19.1% for MAC and 22.5% for RIC (p =.44). Two-year cumulative incidence of relapse (CIR) was 19.8% for MAC and 24.5% for RIC (p =.15). Two-year overall survival (OS) was 61% and 53% for MAC and RIC, respectively (p =.02). Two-year graft-versus-host disease relapse-free survival (GRFS) was 40.8% for MAC and 33.7% for RIC (p =.30). A propensity score-matched analysis was done matching patients for age, HLA match, in vivo T-cell depletion, and Disease Risk Index (DRI). Two-year OS was 67% for MAC, 66% for RIC (p =.95). A subgroup analysis identified that matched related donor transplants benefit from MAC with OS at 2 years 82.6% versus 57.3% for RIC (p =.006). Conclusions: In the matched-related donor setting, MAC regimens may offer superior survival. Overall, for our cohort of predominantly in vivo T-cell depleted patients the outcomes of MAC and RIC were similar.
引用
收藏
页码:553 / 561
页数:9
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