Evidence map›Paper›PMID 42031938›Full record

ArticleScientific reports2026

Deep neural network model for fractional-order cancer chemotherapy dynamics.

Ramsha Shafqat, Imran, Ashraf Al-Quran, Abdelhamid Mohammed Djaouti

Abstract read
In one paragraph

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

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ramsha ShafqatDepartment of Mathematics and Statistics, The University of Lahore, Sargodha, 40100, Pakistan.
ImranInterdisciplinary Research Center for Intelligent Manufacturing Robotics, Dhahran, 31261, Saudi Arabia.
Ashraf Al-QuranDepartment of Mathematics and Statistics, College of Science, King Faisal University, AL-Ahsa, 31982, Saudi Arabia. aalquran@kfu.edu.sa.
Abdelhamid Mohammed DjaoutiDepartment of Mathematics and Statistics, College of Science, King Faisal University, AL-Ahsa, 31982, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This article presents a novel hybrid computational framework for a fractional-order cancer chemotherapy model based on Caputo reaction–diffusion equations. Its main novelty is the coupling of a high-fidelity fractional Adams–Bashforth–Moulton (ABM) predictor–corrector solver with a carefully designed hyperbolic tangent sigmoid deep neural network (HTS–DNN) adapted to nonlocal, memory-dependent tumor–immune–drug dynamics. Unlike standard feed-forward networks using ReLU-type activations, the proposed model employs four hidden layers with (50, 30, 20, 10) neurons, smooth HTS activations, and Levenberg–Marquardt optimization, providing an efficient approximation framework for hereditary fractional trajectories. High-fidelity data generated by the ABM solver are used to train the HTS–DNN with an 80%/10%/10% train/validation/test split. For several fractional orders and initial conditions, the model accurately reproduces the numerical solutions, achieving mean squared errors below [Formula: see text] and uniformly small time-dependent errors. It also provides more than five orders of magnitude reduction in prediction time compared with direct fractional simulation, while preserving key biological features such as memory-driven tumor suppression, delayed immune activation, and concentration-dependent drug effects. These results show that the proposed ABM–HTS–DNN framework is an accurate, robust, and computationally efficient surrogate for fractional cancer chemotherapy dynamics, enabling rapid exploration of therapy schedules and parameter regimes.

Indexed as

Antineoplastic AgentsNeoplasmsNeural Networks, ComputerAlgorithmsComputer SimulationHumansSoft ComputingAntineoplastic AgentsCaputo fractional derivativeCytotoxic therapy modelingHidden-layer designImmune responseLevenberg–Marquardt BackpropagationMathematical modelRadial-basis networksTumor and normal cell populations

Identifiers

PMID42031938
PMCPMC13275890

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LicenceCC BY-NC-ND
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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.