SynthesisEuropean journal of medical research2025
Meta-analysis on the effectiveness and safety of venetoclax-based combination therapy with hypomethylation in acute myeloid leukemia.
Synthesis in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Functional heterogeneity of TP53 mutants in venetoclax-resistant AML: mechanisms, clinical implications, and therapeutic opportunities.Frontiers in oncology · 2026Review
- Genotype-guided comparison of VEN/HMA versus intensive chemotherapy in newly diagnosed intermediate-risk AML: a multicenter real-world study.Blood cancer journal · 2025Article
- Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
The combined therapy strategy of venetoclax with hypomethylating agents (HMAs) has demonstrated encouraging efficacy in the treatment of acute myeloid leukemia (AML), particularly in elderly patients or those deemed unfit for standard treatments. However, due to differences in the research focuses of various research centers, the results have not yet comprehensively and systematically demonstrated the clinical significance of this treatment approach. Therefore, in this meta-analysis, we aimed to assess the effectiveness and safety of venetoclax in combination with HMAs for the treatment of AML. We included a total of 20 clinical studies that met the search criteria, including research focused on AML patients carrying FLT-3 and IDH mutations. Results revealed an overall response (OR) rate of 0.57 and a complete remission (CR)/complete remission with incomplete marrow recovery (CRi) rate of 0.52. Subgroup analyses indicated varying CR/CRi rates among patients with different genetic mutations, with the highest rate observed in IDH mutation carriers at 0.71, FLT-3 mutation carriers at 0.64, and TP53 mutation carriers at 0.44. Simultaneously, we observed adverse events such as anemia, neutropenia, and thrombocytopenia, underscoring the importance of careful management during venetoclax and HMAs treatment. This study emphasizes the potential of venetoclax and HMAs as a promising therapeutic approach for AML while highlighting the critical need for monitoring and managing adverse events in such treatment regimens.
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