ArticleNPJ systems biology and applications2026
Improving severity grading of chemotherapy-induced myelosuppression in AML via data-driven and model-based deep learning.
Article in NPJ systems biology and applications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
Abstract
Chemotherapy-induced myelosuppression in acute myeloid leukemia (AML) frequently leads to life-threatening complications, yet current assessment standards lack the specificity required for personalized risk prediction. We present MM-AI-AML, a two-stage framework merging mechanistic mathematical modeling (MM) with artificial intelligence (AI) to predict myelosuppression severity using pre-treatment clinical data. Initially, a dynamic model simulating post-chemotherapy kinetics across four blood cell lineages was developed to derive a quantitative severity indicator, providing objective labels for 479 AML patients and 900 virtual cases. Subsequently, a TabNet deep learning classifier was trained on 51 clinical features to predict risk. MM-AI-AML demonstrated robust performance, achieving AUCs of 0.85 and 0.78 in internal and external validation cohorts, respectively, significantly outperforming traditional classifiers. Key predictive features included serum albumin, A/G ratio, and lactate dehydrogenase. High-risk stratification by the model was significantly associated with reduced in-hospital survival. By bridging mechanistic insights with interpretable machine learning, MM-AI-AML enables precise, personalized clinical decision-making for managing chemotherapy-related complications in AML.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.