Evidence map›Paper›PMID 40297459›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Discovery of Dynamic Models for AML Disease Progression from Longitudinal Multi-Modal Clinical Data Using Explainable Machine Learning.

Reza Mousavi, Moaath K Mustafa Ali, Daniel Lobo

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

5 · Who and what money

Authors and funding

3 authors.

Reza MousaviDepartment of Biological Sciences, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA.
Moaath K Mustafa AliDepartment of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, 9500 Euclid Avenue, Cleveland, OH 44195, USA.ORCID 0000-0003-3289-2333
Daniel LoboDepartment of Biological Sciences, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, USA.ORCID 0000-0003-4666-6118

Funding

Systems Biology of Shape and Size RegulationR35GM137953 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI Daniel Lobo · 2020 to 2026
$2.3M
NIGMS NIH HHS R35 GM137953
6 · The paper itself

Abstract

Acute Myeloid Leukemia (AML) is a complex and heterogeneous disease identified by severe clinical progression, fast cellular proliferation, and often high mortality rates. Incorporating diverse longitudinal information on patients' medical histories is essential for developing effective disease predictive models applicable to both research and clinical settings. Here, we present a robust methodology for discovering dynamic predictive models to elucidate AML disease progression dynamics from a novel longitudinal multimodal clinical dataset of patients diagnosed with AML. The clinical dataset was analyzed to reveal the main clinical, genetic, and treatment features modulating disease progression. To discover mathematical models-including interactions, parameters, and nodes-predictive of AML progression, we present an explainable machine learning algorithm based on high-performance evolutionary computation. The results demonstrate that the predictive methodology could accurately estimate the clinical dynamics of AML progression in terms of blast percentages for both training and novel patients. This study demonstrates that the developed explainable machine learning approach can successfully predict AML progression by leveraging the heterogeneous and longitudinal dynamics of patients' clinical data. More importantly, this methodology shows significant potential for application in modeling the progression dynamics of other acute diseases, providing a flexible and adaptable framework for advancing clinical and translational research.

Indexed as

Acute Myeloid LeukemiaDisease MarkersDisease Progression PredictionExplainable Machine LearningHigh Performance ComputingLongitudinal Multi-Modal Data

Identifiers

PMID40297459
PMCPMC12036371

What OpenQuestion holds

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Registered trials

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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.