Effects of post-transplant maintenance therapy with decitabine prophylaxis on the relapse for acute lymphoblastic leukemia

被引:10
作者
Fan, Jixin [1 ]
Lu, Runqing [1 ]
Zhu, Jingkui [1 ]
Guo, Xiao [2 ]
Wan, Dingming [1 ]
Xie, Xinsheng [1 ]
Cao, Weijie [1 ]
Zhang, Yinyin [1 ]
Zhao, Haiqiu [1 ]
Li, Yingmei [1 ]
Guo, Rongqun [1 ]
Jiang, Zhongxing [1 ]
Song, Yongping [1 ]
He, Fei [3 ]
Guo, Rong [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Hematol, Zhengzhou, Peoples R China
[2] Zhengzhou Univ, Sch Mat & Chem Engn, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Cardiol, Zhengzhou, Peoples R China
关键词
MINIMAL RESIDUAL DISEASE; ABERRANT DNA METHYLATION; EPIGENETIC ANALYSIS; ADULT; CLASSIFICATION; INFUSION; STANDARD; GRAFT; GVHD; DLI;
D O I
10.1038/s41409-023-01948-y
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In adults with acute lymphoblastic leukemia (ALL), post-transplant relapse is a major risk factor for mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Our study investigated the efficacy and safety of decitabine (dec) with ALL patients post-transplantation. We performed a retrospective cohort study to assess the efficacy of decitabine (dec) with post-transplant ALL at the First Affiliated Hospital of Zhengzhou University from February 2016 to September 2021. A total of 141 consecutive ALL patients were analyzed and divided into decitabine (dec, n = 65) and control (ctrl, n = 76) groups based on whether they were treated with decitabine after allo-HSCT. The 3-year cumulative incidence of relapse (CIR) rate in the dec group was lower than that in the ctrl group (19.6 vs. 36.1%, p = 0.031), with a hazard ratio of 0.491 (95% confidence interval [CI], 0.257-0.936). Additionally, subgroup analyses revealed that the 3-year CIR rate of T-ALL and Ph-negative B-ALL patients in the dec and ctrl groups was 11.7 vs. 35.9% and 19.5 vs. 42.2% (p = 0.035, p = 0.068) respectively. In summary, ALL patients, especially those with T-ALL and Ph-negative B-ALL, may benefit from decitabine as maintenance therapy following allo-HSCT.
引用
收藏
页码:687 / 695
页数:9
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