医学
阿扎胞苷
骨髓增生异常综合症
内科学
累积发病率
髓系白血病
临床终点
移植
造血干细胞移植
白血病
急性白血病
肿瘤科
随机对照试验
骨髓
生物化学
基因表达
DNA甲基化
基因
化学
作者
Oren Pasvolsky,Rima M. Saliba,Uday Popat,Amin M. Alousi,Rohtesh S. Mehta,Jason Yeh,Gheath Alatrash,Masood Adeel,Jeremy Ramdial,David Marín,Gabriela Rondón,Partow Kebriaei,Richard E. Champlin,Naval Daver,Courtney D. DiNardo,Nicholas J. Short,Elizabeth J. Shpall,Betül Oran
标识
DOI:10.1016/j.clml.2024.01.012
摘要
Abstract
Background
Maintenance after allogeneic hematopoietic cell transplantation (alloHCT) with hypomethylating agents has yielded conflicting results. Materials and Methods
We conducted a single center retrospective matched-control analysis with the study group (5-azacitidine [AZA] group) including adults with FLT3-negative acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) who received post-transplant AZA maintenance off clinical trial (n = 93). A matched control group was comprised of contemporaneous AML/MDS patients who did not receive any maintenance (n = 357). Primary endpoint was disease progression. Results
The AZA and control groups had comparable patient and disease characteristics except for older age (median: 61 vs. 57 years, P = .01) and lower hematopoietic comorbidity index (median: 2 vs. 3, P = .04) in the AZA group. The 3-year cumulative incidence of progression in the AZA and control groups was 29% vs. 33% (P = .09). The protective effect of AZA on progression was limited to patients with high-risk AML/MDS (HR = 0.4, 95% CI=0.2-0.8, P = .009). This led to improved progression-free survival both in high-risk AML and MDS patients with maintenance (HR = 0.2, 95% CI=0.1-0.6, P = .004 and HR=0.4, 95% CI=0.2-0.9, P = .04). Conclusion
AZA maintenance was associated with a lower progression rate in patients with high-risk FLT3-negative AML or MDS, and AZA maintenance should be considered for post-alloHCT maintenance in this subset.
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