Comparison of autologous, matched sibling, and alternative donor stem cell transplant outcomes for acute myeloid leukemia patients in first remission: A propensity score matching study

Author:

Wang Mingyang12,Zhang Haixiao12,Zheng Xinhui12ORCID,Liu Jia12,Wang Jiali12,Cao Yigeng12,Zhang Xiaoyu12,Zhang Rongli12,Chen Xin12,Zhai Weihua12,Ma Qiaoling12,Wei Jialin12,Huang Yong12,Yang Donglin12,He Yi12,Pang Aiming12,Feng Sizhou12,Han Mingzhe12,Jiang Erlie12ORCID

Affiliation:

1. State Key Laboratory of Experimental Hematology National Clinical Research Center for Blood Diseases Haihe Laboratory of Cell Ecosystem Institute of Hematology & Blood Diseases Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Tianjin China

2. Tianjin Institutes of Health Science Tianjin China

Abstract

AbstractAutologous hematopoietic stem cell transplantation (auto‐HSCT), matched sibling donor HSCT (MSD‐HSCT), and alternative donor HSCT (AD‐HSCT) are viable post‐remission treatment options for acute myeloid leukemia (AML). A total of 283 de novo favorable‐ and intermediate‐risk AML patients, based on the ELN 2022 criteria, in first complete remission were initially included for propensity score matching. Following the matching process, 126 patients were selected for further analysis, with 42 patients in each of the auto‐HSCT, MSD‐HSCT, and AD‐HSCT groups. Among the AD‐HSCT group, 38 of 42 (90.5%) patients received haploidentical HSCT. In patients with persistent undetectable measurable residual disease (uMRD) before transplant (n = 83), overall survival (OS) was similar across the groups. However, auto‐HSCT showed a trend of increased disease‐free survival (DFS) compared to AD‐HSCT (HR 2.85, P = 0.09), resulting in a 3‐year DFS and OS of 79.1% and 82.8%, respectively. In the non‐persistent uMRD group (n = 38), auto‐HSCT exhibited a tendency to increase the risk of relapse, particularly when compared to AD‐HSCT (HR 0.24, P = 0.07), but this did not result in inferior OS. The monthly direct medical cost per patient within the first 2 years after HSCT was significantly lower in auto‐HSCT compared to MSD‐HSCT (P = 0.015) and AD‐HSCT (P < 0.001). Our results provide evidence for the use of auto‐HSCT as a viable therapeutic option for favorable‐ and intermediate‐risk de novo AML patients in first complete remission with persistent uMRD. Additionally, our findings demonstrated a notable cost advantage associated with auto‐HSCT compared to MSD‐HSCT and AD‐HSCT.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cancer Research,Oncology,Hematology,General Medicine

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