Antithymocyte globulin for graft-versus-host disease prophylaxis: an updated systematic review and meta-analysis

被引:33
|
作者
Kumar, Ambuj [1 ]
Reljic, Tea [1 ]
Hamadani, Mehdi [2 ]
Mohty, Mohamad [3 ,4 ]
Kharfan-Dabaja, Mohamed A. [5 ]
机构
[1] Univ S Florida, Morsani Coll Med, Program Comparat Effectiveness Res, Tampa, FL 33620 USA
[2] Med Coll Wisconsin, Div Hematol Oncol, Milwaukee, WI 53226 USA
[3] Univ Paris 06, St Antoine Hosp, Dept Haematol, Paris, France
[4] INSERM, UMRs938, Paris, France
[5] Mayo Clin, Blood & Marrow Transplantat Program, Div Hematol Oncol, Jacksonville, FL 32224 USA
关键词
STEM-CELL TRANSPLANTATION; ANTI-THYMOCYTE GLOBULIN; BONE-MARROW-TRANSPLANTATION; LEUKEMIA WORKING PARTY; SEVERE APLASTIC-ANEMIA; UNRELATED DONORS; SIBLING DONOR; FREE SURVIVAL; ALLOGENEIC TRANSPLANTATION; MYELOGENOUS LEUKEMIA;
D O I
10.1038/s41409-018-0393-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Graft-versus-host disease (GVHD) remains a limiting factor for successful allogeneic hematopoietic cell transplantation (allo-HCT). Conflicting data exist on the benefit of ATG on post-transplant survival. We performed a systematic review of randomized controlled trials (RCTs) to assess benefits and harms of thymoglobulin and Fresenius (re-branded as Grafalon) ATG formulations in patients undergoing allo-HCT for a variety of hematologic malignancies and bone marrow failure syndromes. A comprehensive search of MEDLINE, EMBASE, and Cochrane Library was performed. Data on methodological quality, benefits, and harms were extracted for each trial and pooled under a random-effects model. Eight RCTs (1134 patients) met the inclusion criteria. Methodological quality ranged from moderate to very low. Pooled results showed no difference in overall survival (OS) with the use of ATG (hazard ratio (HR) = 0.97; 95% confidence interval (CI) = 0.74-1.28; P = 0.83). ATG reduced grade II/III acute GVHD (risk ratio (RR) = 0.61; 95% CI = 0.48-0.77; P < 0.0001), grade III/IV acute GVHD (RR = 0.52; 95% CI = 0.34-0.81; P = 0.004), and chronic GVHD (RR = 0.52; 95% CI = 0.40-0.69; P < 0.00001) without an increase in non-relapse mortality (NRM) (RR = 0.91; 95% CI = 0.74-1.13; P = 0.40). Future studies with better methodological quality are needed to provide conclusive answers related to optimal dosing and timing of ATG for prevention of GVHD.
引用
收藏
页码:1094 / 1106
页数:13
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