Anti-thymocyte globulin combined with post-transplantation cyclophosphamide reduce graft-versus-host disease in hematopoietic stem cell transplantation for pediatric leukemia.

IF 2.2 4区 医学 Q3 HEMATOLOGY
Mengze Hu, Junhui Li, Tao Hu, Zhaoxia Zhang, Shunqiao Feng, Litian Xuan, Rong Liu
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Abstract

This retrospective analysis evaluated the use of anti-thymocyte globulin (ATG) with or without post-transplantation cyclophosphamide (PTCy) for graft-versus-host disease (GvHD) prophylaxis in children with acute leukemia undergoing hematopoietic stem cell transplantation (HSCT). The study included 57 children, with 35 in the ATG-PTCy group and 22 in the ATG group. While overall incidence of acute and chronic GvHD did not differ significantly between groups, the ATG-PTCy group had lower rates of grade II-IV acute GvHD (p = 0.013) and moderate-to-severe chronic GvHD (p = 0.001) compared to the ATG group. Importantly, ATG-PTCy significantly improved GvHD/relapse-free survival (GRFS) compared to ATG (65.71% vs. 36.63%; p = 0.003). There were no differences in engraftment, infection rates, immune reconstitution, overall survival, leukemia-free survival, relapse rate, or non-relapse mortality between the two groups. Combining ATG with PTCy may reduce moderate-to-severe GvHD and improve GRFS in children undergoing HSCT for acute leukemia.

抗胸腺细胞球蛋白与移植后环磷酰胺联合使用可减少小儿白血病造血干细胞移植中的移植物抗宿主疾病。
这项回顾性分析评估了在接受造血干细胞移植(HSCT)的急性白血病患儿中使用抗胸腺细胞球蛋白(ATG)联合或不联合移植后环磷酰胺(PTCy)预防移植物抗宿主病(GvHD)的情况。这项研究包括57名儿童,其中ATG-PTCy组35人,ATG组22人。虽然急性和慢性并发症的总体发生率在各组间无显著差异,但与ATG组相比,ATG-PTCy组的II-IV级急性并发症(p = 0.013)和中度至重度慢性并发症(p = 0.001)发生率较低。重要的是,与ATG组相比,ATG-PTCy能显著提高抗排异/无复发生存率(GRFS)(65.71% vs. 36.63%; p = 0.003)。两组在移植、感染率、免疫重建、总生存期、无白血病生存期、复发率或非复发死亡率方面没有差异。在接受造血干细胞移植治疗急性白血病的儿童中,ATG与PTCy联合治疗可减少中度至重度GvHD,提高GRFS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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