Evidence map›Paper›PMID 41904443›Full record

ArticleBMC cancer2026

The prognostic value of maintaining minimal residual disease status in patients with acute myeloid leukaemia receiving azacitidine-based therapy.

Jun-Fang Wang, Juan Cheng

Abstract read
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Jun-Fang WangFirst Clinical Medical College of Lanzhou University, Lanzhou, China.
Juan ChengFirst Clinical Medical College of Lanzhou University, Lanzhou, China. Chenggu029@163.com.

Funding

Analysis of the Efficacy and Safety of Azacitidine in Maintenance Therapy for Acute Myeloid Leukemia 071101546
6 · The paper itself

Abstract

Multiparametric flow cytometry (MFC) is the core method for monitoring measurable residual disease (MRD) in acute myeloid leukemia (AML), yet its clinical value during azacitidine-based maintenance therapy lacks sufficient real-world data support. This study retrospectively enrolled 129 AML patients who received azacitidine maintenance therapy at the First Hospital of Lanzhou University from January 2019 to May 2025, aiming to explore the aforementioned clinical value and related prognostic factors. The primary endpoints of the study were overall survival (OS), relapse-free survival (RFS), and disease-free survival (DFS); the secondary endpoints included time to MRD negativity, duration of MRD negativity, and the incidence of adverse events.The results showed that azacitidine-based maintenance therapy could bring significant clinical benefits to AML patients. MRD status and duration of response (DoR) during the maintenance phase were core prognostic biomarkers for AML patients receiving this treatment. Among them, the duration of MRD negativity was predictive of longer OS, DFS, and RFS, which could effectively reflect a robust therapeutic response and is recommended as a dynamic endpoint for evaluating maintenance therapy efficacy. In terms of safety, the incidence of serious adverse events in both the maintenance group and the control group was within a manageable range, with no intolerable safety issues. In conclusion, azacitidine-based maintenance therapy for AML has a favorable benefit-risk ratio, and MRD-related indicators can serve as key reference criteria for evaluating the efficacy and prognosis of this treatment regimen.

Indexed as

Antimetabolites, AntineoplasticAntineoplastic Combined Chemotherapy ProtocolsAzacitidineLeukemia, Myeloid, AcuteNeoplasm, ResidualAdultAgedDisease-Free SurvivalFemaleFlow CytometryHumansMaintenance ChemotherapyMaleMiddle AgedPrognosisRetrospective StudiesAntimetabolites, AntineoplasticAzacitidineAMLMaintenance therapyMinimal residual disease azacitidineTherapeutic effects

Identifiers

PMID41904443
PMCPMC13159310

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.