# Comparison of maintenance with decitabine or chemotherapy in a real-world cohort of patients with acute myeloid leukemia

**Authors:** Zhi-Feng Wei, Jia-Qi Yan, Ye-Hui Tan, Hai Lin, Qiu-Ju Liu, Xiao-Liang Liu, Long Su, Su-Jun Gao

PMC · DOI: 10.3389/fphar.2026.1753030 · Frontiers in Pharmacology · 2026-02-13

## TL;DR

This study compares decitabine and chemotherapy for maintenance therapy in AML patients, finding both effective but with decitabine showing better tolerability and survival in some groups.

## Contribution

The study provides real-world evidence on the comparative efficacy and safety of decitabine versus chemotherapy in AML maintenance therapy.

## Key findings

- Maintenance therapy improved relapse-free and overall survival in AML patients.
- Decitabine showed better tolerability and survival benefits in specific subgroups.
- No significant difference in outcomes between decitabine and chemotherapy overall.

## Abstract

The objective of this real-world cohort study was to evaluate the efficacy and safety of decitabine versus conventional chemotherapy in the maintenance therapy (MT) of patients with acute myeloid leukemia (AML).

Data were collected from 156 consecutive patients diagnosed with AML at our center. All patients achieved complete remission (CR) after 1–2 courses of induction therapy, followed by consolidation with high-dose cytarabine (HiDAC). MT was administered using either decitabine or conventional chemotherapy, while patients who did not receive maintenance served as controls.

MT significantly improved both relapse-free survival (RFS) and overall survival (OS) in AML patients. However, no significant difference was observed between decitabine and conventional chemotherapy. MT notably prolonged both RFS and OS in the cytogenetic intermediate-risk group, patients without FLT3-ITD mutations, and those achieving CR after one course of induction therapy. The benefits of MT were not influenced by the European Leukemia Net (ELN) risk category, measurable residual disease (MRD) status, or the number of HiDAC courses. Compared with chemotherapy, decitabine maintenance significantly improved RFS and OS in patients who received 3–4 courses of treatment. Additionally, the incidence of adverse reactions was significantly lower in the decitabine group than in the chemotherapy arm.

MT with either decitabine or chemotherapy can improve outcomes of AML patients in this real-world cohort. Decitabine maintenance exhibits better tolerability compared with chemotherapy and enhances survival in specific patient subgroups.

## Linked entities

- **Genes:** FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322]
- **Chemicals:** decitabine (PubChem CID 451668), cytarabine (PubChem CID 6253)
- **Diseases:** acute myeloid leukemia (MONDO:0015667)

## Full-text entities

- **Genes:** BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, NPM1 (nucleophosmin 1) [NCBI Gene 4869] {aka B23, NPM}, FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}, DNMT3A (DNA methyltransferase 3 alpha) [NCBI Gene 1788] {aka DNMT3A2, HESJAS, M.HsaIIIA, TBRS}
- **Diseases:** anemia (MESH:D000740), hematological toxicities (MESH:D006402), neutropenia (MESH:D009503), death (MESH:D003643), ELN (MESH:D007938), X-LL (MESH:D000326), infection (MESH:D007239), thrombocytopenia (MESH:D013921), gastrointestinal adverse reactions (MESH:D005767), toxicities (MESH:D064420), acute promyelocytic leukemia (MESH:D015473), liver toxicity (MESH:D056486), liver dysfunction (MESH:D017093), febrile neutropenia (MESH:D064147), pulmonary infection (MESH:D012141), HL (MESH:C538324), agranulocytosis (MESH:D000380), myeloplastic syndrome (MESH:D013577), perianal infection (MESH:D000694), MT (MESH:D007319), rash (MESH:D005076), leukopenia (MESH:D007970), nausea (MESH:D009325), diarrhea (MESH:D003967), pneumonia (MESH:D011014), AML (MESH:D015470), fever (MESH:D005334), MDS (MESH:D009190), vomiting (MESH:D014839)
- **Chemicals:** DCAG (-), AA (MESH:D015250), quizartinib (MESH:C544967), cytarabine (MESH:D003561), homoharringtonine (MESH:D000077863), midostaurin (MESH:C059539), azacitidine (MESH:D001374), idarubicin (MESH:D015255), enasidenib (MESH:C000605269), DA (MESH:C025953), venetoclax (MESH:C579720), gilteritinib (MESH:C000609080), daunorubicin (MESH:D003630), sorafenib (MESH:D000077157), Dec (MESH:D000077209), ivosidenib (MESH:C000627630)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946668/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946668/full.md

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Source: https://tomesphere.com/paper/PMC12946668