Experience with second allogeneic hematopoietic stem cell transplantation in Chilean patients: A single-center study.

Yorman Flores, Javier Díaz, Patricio Rojas, José Salinas, Catherine Gutiérrez, Marcela Vidal, Verónica Jara, Elizabeth Rivera, María José García, Vicente Sandoval, Felipe Palacios, Maximiliano Vergara, Mauricio Ocqueteau, Mauricio Sarmiento
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Abstract

Introduction: Allogeneic hematopoietic stem cell transplantation is potentially a curative treatment for several hematological diseases. However, post-transplant relapse remains a significant challenge. For patients who achieve a second complete remission, a second allogeneic transplantation may be a promising therapeutic option. The aim of this study was to analyze clinical outcomes including graft-versus-host disease, non-relapse mortality, and relapse rates, as well as graft sources in patients who underwent a second allogeneic transplantation in a university-based transplant program.

Patients and methods: A retrospective analysis of 21 adult patients who underwent a second allogeneic transplantation between 2001 and 2023 was performed. Data on demographics, underlying disease, graft source, conditioning, graft-versus-host disease, relapse, and survival were collected. Survival estimates were calculated using the Kaplan-Meier method.

Results: The graft source was bone marrow in 60 % and peripheral blood in 40 % of cases. Grade III-IV acute graft-versus-host disease occurred in 5 % and extensive chronic graft-versus-host disease in 17 %. The non-relapse mortality was 69.2 %, and disease relapse occurred in 23.1 %. The one-year progression-free survival was 26.5 %, and overall survival was 42.3 %. Compared to those transplanted before 2010, patients who underwent transplantation after 2010 showed improved two-year PFS and OS, reaching 55 % and 45.4 %, respectively.

Conclusion: A second allogeneic transplantation may offer a survival benefit in selected patients with relapsed hematologic malignancies or bone marrow failure syndromes. Despite high non-relapse mortality, outcomes have improved in recent years with better salvage strategies.

智利患者第二次异体造血干细胞移植的经验:一项单中心研究。
异体造血干细胞移植是治疗多种血液病的潜在治疗方法。然而,移植后复发仍然是一个重大挑战。对于实现第二次完全缓解的患者,第二次异体移植可能是一个有希望的治疗选择。本研究的目的是分析临床结果,包括移植物抗宿主病、非复发死亡率和复发率,以及在大学移植项目中接受第二次同种异体移植的患者的移植物来源。患者和方法:对2001年至2023年间接受第二次同种异体移植的21例成人患者进行回顾性分析。收集了人口统计学、基础疾病、移植物来源、调节、移植物抗宿主病、复发和生存的数据。生存估计采用Kaplan-Meier法计算。结果:骨髓移植占60%,外周血移植占40%。III-IV级急性移植物抗宿主病发生率为5%,广泛的慢性移植物抗宿主病发生率为17%。未复发死亡率为69.2%,疾病复发率为23.1%。一年无进展生存率为26.5%,总生存率为42.3%。与2010年之前移植的患者相比,2010年之后移植的患者两年PFS和OS改善,分别达到55%和45.4%。结论:第二次同种异体移植可能为复发的恶性血液病或骨髓衰竭综合征患者提供生存益处。尽管非复发死亡率很高,但近年来由于更好的抢救策略,结果有所改善。
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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