[Allogeneic hematopoietic stem cell transplantation for 510 patients with active relapsed/refractory acute myeloid leukemia: a real-world study].

Q3 Medicine
X Y Man, M L Li, X H Fei, H Y Cheng, Y M Yin, R M Luo, S Q Zhang, J Y Gu, S Xue, W J Zhang, F Yang, Q H Man, Y X Yang, Z Q Tian, T T Li, L Yuan, H X Wen, W Wei, W J Wang, Y Wang, J B Wang
{"title":"[Allogeneic hematopoietic stem cell transplantation for 510 patients with active relapsed/refractory acute myeloid leukemia: a real-world study].","authors":"X Y Man, M L Li, X H Fei, H Y Cheng, Y M Yin, R M Luo, S Q Zhang, J Y Gu, S Xue, W J Zhang, F Yang, Q H Man, Y X Yang, Z Q Tian, T T Li, L Yuan, H X Wen, W Wei, W J Wang, Y Wang, J B Wang","doi":"10.3760/cma.j.cn121090-20260120-00040","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To investigate the long-term survival outcomes of salvage allogeneic hematopoietic stem cell transplantation (R/R AML) . <b>Methods:</b> This was a retrospective real-world study. We conducted a retrospective analysis of 510 patients with R/R AML who underwent allo-HSCT at Aerospace Center Hospital between July 2012 and December 2024. All patients had active disease before transplantation, defined as a bone marrow blast proportion of at least 5%. Overall survival (OS) and disease-free survival (DFS) were assessed using the Kaplan-Meier method, whereas the cumulative incidence of relapse (CIR) and non-relapse mortality (NRM) were evaluated by competing-risk models. Univariate analysis was performed using the log-rank test, and multivariable analysis was conducted using Cox regression for survival outcomes and Fine-Gray regression for competing-risk outcomes to identify independent prognostic factors. <b>Results:</b> In this cohort of 510 patients, the median follow-up duration was 50 months (range, 0-151 months). The estimated 10-year overall survival (OS) and disease-free survival (DFS) rates were 35.5% (95% <i>CI</i>: 31.2% -40.5% ) and 33.2% (95% <i>CI</i>: 29.1% -38.0% ), respectively. Multivariable analysis demonstrated that European LeukemiaNet (ELN) risk stratification was a core prognostic factor. Patients in the intermediate-risk (<i>HR</i>=1.74, <i>P</i>=0.002) and adverse-risk (<i>HR</i>=1.97, <i>P</i><0.001) categories had markedly lower OS and DFS rates. Mild-to-moderate chronic graft-versus-host disease (cGVHD) served as a protective factor for OS and DFS (both <i>P</i><0.001). A diagnosis-to-transplant interval longer than 10 months (<i>HR</i>=1.56, <i>P</i><0.001) was correlated with poor survival outcomes. A higher infused CD34(+) cell dose (≥4.3×10(6)/kg) was independently associated with superior OS (<i>HR</i>=0.64, <i>P</i><0.001) and DFS (<i>HR</i>=0.62, <i>P</i><0.001). In competing-risk analysis, intermediate and adverse ELN risk stratification (<i>HR</i>=2.73 and 2.90, respectively; both <i>P</i><0.001) and elevated bone marrow blast percentage (≥50% ) (<i>HR</i>=1.62, <i>P</i>=0.037) were independently linked to increased relapse risk. Mild, moderate, and severe cGVHD, compared with no cGVHD (<i>HR</i>=0.38, 0.13, and 0.24; <i>P</i><0.001, <i>P</i><0.001, and <i>P</i>=0.015, respectively), and grade Ⅲ-Ⅳ acute graft-versus-host disease (aGVHD) (<i>HR</i>=0.54, <i>P</i>=0.033) were associated with a lower CIR. Regarding non-relapse mortality (NRM), grade Ⅲ-Ⅳ aGVHD (<i>HR</i>=2.36, <i>P</i><0.001) and severe cGVHD (<i>HR</i>=2.74, <i>P</i><0.001) were major risk factors, and advanced age (<i>HR</i>=1.47, <i>P</i>=0.033) was also associated with higher NRM. <b>Conclusions:</b> This study indicates that long-term disease-free survival may be attained through salvage allo-HSCT in patients with R/R AML despite active disease at transplantation. Long-term outcomes are mainly determined by disease biology and post-transplant immune effects, with ELN risk stratification and GVHD playing dominant roles, whereas pre-transplant tumor burden mainly affects relapse risk but is not an independent determinant of long-term survival. These findings suggest that greater emphasis should be placed on risk stratification and transplantation timing in clinical practice, rather than solely pursuing complete remission prior to transplantation.</p>","PeriodicalId":24016,"journal":{"name":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","volume":"47 6","pages":"534-540"},"PeriodicalIF":0.0000,"publicationDate":"2026-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13575536/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/cma.j.cn121090-20260120-00040","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To investigate the long-term survival outcomes of salvage allogeneic hematopoietic stem cell transplantation (R/R AML) . Methods: This was a retrospective real-world study. We conducted a retrospective analysis of 510 patients with R/R AML who underwent allo-HSCT at Aerospace Center Hospital between July 2012 and December 2024. All patients had active disease before transplantation, defined as a bone marrow blast proportion of at least 5%. Overall survival (OS) and disease-free survival (DFS) were assessed using the Kaplan-Meier method, whereas the cumulative incidence of relapse (CIR) and non-relapse mortality (NRM) were evaluated by competing-risk models. Univariate analysis was performed using the log-rank test, and multivariable analysis was conducted using Cox regression for survival outcomes and Fine-Gray regression for competing-risk outcomes to identify independent prognostic factors. Results: In this cohort of 510 patients, the median follow-up duration was 50 months (range, 0-151 months). The estimated 10-year overall survival (OS) and disease-free survival (DFS) rates were 35.5% (95% CI: 31.2% -40.5% ) and 33.2% (95% CI: 29.1% -38.0% ), respectively. Multivariable analysis demonstrated that European LeukemiaNet (ELN) risk stratification was a core prognostic factor. Patients in the intermediate-risk (HR=1.74, P=0.002) and adverse-risk (HR=1.97, P<0.001) categories had markedly lower OS and DFS rates. Mild-to-moderate chronic graft-versus-host disease (cGVHD) served as a protective factor for OS and DFS (both P<0.001). A diagnosis-to-transplant interval longer than 10 months (HR=1.56, P<0.001) was correlated with poor survival outcomes. A higher infused CD34(+) cell dose (≥4.3×10(6)/kg) was independently associated with superior OS (HR=0.64, P<0.001) and DFS (HR=0.62, P<0.001). In competing-risk analysis, intermediate and adverse ELN risk stratification (HR=2.73 and 2.90, respectively; both P<0.001) and elevated bone marrow blast percentage (≥50% ) (HR=1.62, P=0.037) were independently linked to increased relapse risk. Mild, moderate, and severe cGVHD, compared with no cGVHD (HR=0.38, 0.13, and 0.24; P<0.001, P<0.001, and P=0.015, respectively), and grade Ⅲ-Ⅳ acute graft-versus-host disease (aGVHD) (HR=0.54, P=0.033) were associated with a lower CIR. Regarding non-relapse mortality (NRM), grade Ⅲ-Ⅳ aGVHD (HR=2.36, P<0.001) and severe cGVHD (HR=2.74, P<0.001) were major risk factors, and advanced age (HR=1.47, P=0.033) was also associated with higher NRM. Conclusions: This study indicates that long-term disease-free survival may be attained through salvage allo-HSCT in patients with R/R AML despite active disease at transplantation. Long-term outcomes are mainly determined by disease biology and post-transplant immune effects, with ELN risk stratification and GVHD playing dominant roles, whereas pre-transplant tumor burden mainly affects relapse risk but is not an independent determinant of long-term survival. These findings suggest that greater emphasis should be placed on risk stratification and transplantation timing in clinical practice, rather than solely pursuing complete remission prior to transplantation.

[同种异体造血干细胞移植治疗510例活动性复发/难治性急性髓系白血病:一项现实世界研究]。
目的:探讨补救性异基因造血干细胞移植(R/R AML)的长期生存预后。方法:这是一项真实世界的回顾性研究。我们对2012年7月至2024年12月在航空航天中心医院接受同种异体造血干细胞移植的510例R/R AML患者进行了回顾性分析。所有患者在移植前均有活动性疾病,定义为骨髓母细胞比例至少为5%。总生存期(OS)和无病生存期(DFS)采用Kaplan-Meier法评估,而累积复发发生率(CIR)和非复发死亡率(NRM)采用竞争风险模型评估。单因素分析采用log-rank检验,多因素分析采用生存结局的Cox回归和竞争风险结局的Fine-Gray回归,以确定独立的预后因素。结果:在510例患者中,中位随访时间为50个月(范围0-151个月)。估计的10年总生存率(OS)和无病生存率(DFS)分别为35.5% (95% CI: 31.2% -40.5%)和33.2% (95% CI: 29.1% -38.0%)。多变量分析表明,欧洲白血病(ELN)风险分层是一个核心的预后因素。中危(HR=1.74, P=0.002)和危(HR=1.97, PPHR=1.56, PHR=0.64, PHR=0.62, PHR=2.73, 2.90, PHR均=1.62,P=0.037)患者与复发风险增加独立相关。与无cGVHD相比,轻度、中度和重度cGVHD (HR=0.38、0.13和0.24;PPP分别=0.015)和Ⅲ-Ⅳ级急性移植物抗宿主病(aGVHD) (HR=0.54, P=0.033)与较低的CIR相关。关于非复发死亡率(NRM),Ⅲ-Ⅳ级aGVHD (HR=2.36, PHR=2.74, PHR=1.47, P=0.033)也与较高的NRM相关。结论:这项研究表明,尽管移植时疾病活跃,但通过补救性异源造血干细胞移植,R/R AML患者可以获得长期无病生存。长期预后主要由疾病生物学和移植后免疫效应决定,其中ELN风险分层和GVHD起主导作用,而移植前肿瘤负担主要影响复发风险,但不是长期生存的独立决定因素。这些发现表明,在临床实践中应该更加重视风险分层和移植时机,而不是仅仅追求移植前的完全缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.80
自引率
0.00%
发文量
100
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书