Program for Comparative Effectiveness Research, University of South Florida Morsani College of Medicine, Tampa, FL, USA.
Division of Hematology/Oncology, Medical College of Wisconsin, Milwaukee, WI, USA.
Bone Marrow Transplant. 2019 Jul;54(7):1094-1106. doi: 10.1038/s41409-018-0393-0. Epub 2018 Nov 16.
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.
移植物抗宿主病(GVHD)仍然是异体造血细胞移植(allo-HCT)成功的限制因素。关于 ATG 对移植后生存的益处,存在相互矛盾的数据。我们对随机对照试验(RCTs)进行了系统评价,以评估在接受各种血液系统恶性肿瘤和骨髓衰竭综合征的 allo-HCT 患者中使用胸腺球蛋白和 Fresenius(重新命名为 Grafalon)ATG 制剂的益处和危害。对 MEDLINE、EMBASE 和 Cochrane Library 进行了全面检索。为每个试验提取了方法学质量、益处和危害的数据,并在随机效应模型下进行了汇总。八项 RCT(1134 例患者)符合纳入标准。方法学质量从中等到非常低不等。汇总结果显示,使用 ATG 治疗在总体生存(OS)方面没有差异(风险比(HR)=0.97;95%置信区间(CI)=0.74-1.28;P=0.83)。ATG 降低了 II/III 级急性 GVHD(风险比(RR)=0.61;95%CI=0.48-0.77;P<0.0001)、III/IV 级急性 GVHD(RR=0.52;95%CI=0.34-0.81;P=0.004)和慢性 GVHD(RR=0.52;95%CI=0.40-0.69;P<0.00001),而无复发死亡率(NRM)增加(RR=0.91;95%CI=0.74-1.13;P=0.40)。需要进行具有更好方法学质量的未来研究,以提供有关 ATG 预防 GVHD 的最佳剂量和时间的明确答案。