Efficacy of epigenetic agents for older patients with acute myeloid leukemia and myelodysplastic syndrome in randomized controlled trials: a systematic review and network meta-analysis

被引:4
|
作者
Oh, SuA [1 ]
Kim, EunYoung [1 ]
机构
[1] Chung Ang Univ, Coll Pharm, Dept Hlth Social & Clin Pharm, Data Sci Evidence Based & Clin Res Lab, Seoul 06974, South Korea
基金
新加坡国家研究基金会;
关键词
Epigenetic; AML; MDS; Network meta-analysis; Older; STEM-CELL TRANSPLANTATION; LOW-DOSE DECITABINE; PHASE-III; HYPOMETHYLATING AGENTS; SUPPORTIVE CARE; OPEN-LABEL; AZACITIDINE; 5-AZA-2'-DEOXYCYTIDINE; AML; L1210;
D O I
10.1007/s10238-023-01041-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) are hematologic malignancies that mostly affect the elderly and have poor prognoses. Mutations in epigenetic regulatory genes cause AML/MDS through changes in DNA methylation and histone modifications. Some epigenetic agents are used in patients with AML and MDS. However, most studies have focused on azacitidine (AZA) or decitabine (DEC), and few studies have been conducted on combination therapies or other epigenetic therapies. This network meta-analysis (NMA) aimed to compare the efficacy of epigenetic agents overall in patients with AML and MDS. A systematic review and NMA of all available II-III phase randomized controlled trials (RCTs) comparing epigenetic agents were performed. The Embase and PubMed databases were searched for relevant studies. The Bayesian model was used in the NMA, and the surface under the cumulative ranking curve (SUCRA) was used to rank comparisons. The primary endpoint was overall survival (OS), and the secondary endpoints were complete response (CR) and partial response (PR). OS was extended by AZA + venetoclax (SUCRA 0.94) in patients with AML and MDS. DEC (SUCRA 0.78) relatively improved CR and PR. In this study, AZA-related treatment was relatively effective in improving the OS of patients with AML and MDS, and DEC-related treatment showed a relatively high effect on CR and PR. The protocol for this systematic review was registered with the International Prospective Register of Systematic Reviews (CRD42022303601).
引用
收藏
页码:2705 / 2714
页数:10
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