Evidence map›Paper›PMID 40410237›Full record

ArticleNPJ systems biology and applications2025

Personalizing neoadjuvant chemotherapy regimens for triple-negative breast cancer using a biology-based digital twin.

Chase Christenson, Chengyue Wu, David A Hormuth, Jingfei Ma, Clinton Yam, Gaiane M Rauch, Thomas E Yankeelov

Abstract read
In one paragraph

Article in NPJ systems biology and applications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. The future of mathematical oncology in the age of AI.NPJ systems biology and applications · 2026
    Review
  3. Review
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

7 authors.

Chase ChristensonDepartments of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA. chase.christenson@utexas.edu.
Chengyue WuOden Institute for Computational Engineering and Sciences, The University of Texas at Austin, Austin, TX, USA.
David A HormuthOden Institute for Computational Engineering and Sciences, The University of Texas at Austin, Austin, TX, USA.
Jingfei MaDepartments of Imaging Physics, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Clinton YamDepartments of Breast Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Gaiane M RauchDepartments of Breast Imaging, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Thomas E YankeelovDepartments of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA. tey@utexas.edu.

Funding

Quantitative MRI for Predicting Response of Breast Cancer to Neoadjuvant TherapyU01CA142565 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KARCZMAR, GREGORY S., NANDA, RITA · 2010 to 2019
$4.5M
INTEGRATING OMICS AND QUANTITATIVE IMAGING DATA IN CO-CLINICAL TRIALS TO PREDICT TREATMENT RESPONSE IN TRIPLE NEGATIVE BREAST CANCERU24CA226110 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LEWIS, MICHAEL T., RUBIN, DANIEL L · 2019 to 2023
$3.2M
Image Driven Multi-Scale Modeling to Predict Treatment Response in Breast CancerU01CA174706 · NCI · VANDERBILT UNIVERSITY · PI QUARANTA, VITO, YANKEELOV, THOMAS E · 2013 to 2018
$2.5M
Cancer Prevention and Research Institute of Texas RR160005NCI NIH HHS U01 CA142565NCI NIH HHS U01CA142565NCI NIH HHS U01 CA174706NCI NIH HHS U24 CA226110
6 · The paper itself

Abstract

Despite advances triple negative breast cancer treatment, ~50% of patients will not achieve a pathological complete response prior to surgery with standard of care neoadjuvant therapy (NAT). We hypothesize that personalized regimens for NAT could significantly improve patient outcomes, which we address with a patient-specific digital twin framework. This framework is established by calibrating a biology-based model to longitudinal magnetic resonance images with approximate Bayesian computation. We then apply optimal control theory to either (1) reduce the final tumor cell number with equivalent dose, or (2) reduce the total dose of NAT with equivalent response. For (1), the personalized regimens (n = 50) achieved a median (range) reduction in the final tumor cell number of 17.62% (0.00-37.36%). For (2), the personalized regimens achieved a median reduction in dose delivered of 12.62% (0.00-56.55%) when compared to the standard-of-care regimen, while providing statistically equivalent tumor control.

Indexed as

Neoadjuvant TherapyPrecision MedicineTriple Negative Breast NeoplasmsBayes TheoremFemaleHumansMagnetic Resonance Imaging

Identifiers

PMID40410237
PMCPMC12102339

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.