Evidence map›Paper›PMID 40587816›Full record

ArticleJCO clinical cancer informatics2025

Linear Federated Learning for Outcome Prediction With Application to Hepatocellular Carcinoma Radiotherapy.

Keyur D Shah, Harald Paganetti, Pablo Yepes, Theodore S Hong, Jennifer Y Wo, J Hannah Roberts, Eugene J Koay, Christian V Guthier, Ibrahim Chamseddine

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 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
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0citing papers in PubMed
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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

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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

9 authors.

Keyur D ShahDepartment of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0002-0886-655X
Harald PaganettiDepartment of Radiation Oncology, Mass General Brigham, Harvard Medical School, Boston, MA.
Pablo YepesDepartment of Physics and Astronomy, Rice University, Houston, TX.
Theodore S HongDepartment of Radiation Oncology, Mass General Brigham, Harvard Medical School, Boston, MA.ORCID 0000-0001-8481-6581
Jennifer Y WoDepartment of Radiation Oncology, Mass General Brigham, Harvard Medical School, Boston, MA.
J Hannah RobertsDepartment of Radiation Oncology, Mass General Brigham, Harvard Medical School, Boston, MA.
Eugene J KoayDepartment of Radiation Oncology, University of Texas, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-7675-3461
Christian V GuthierDepartment of Radiation Oncology, Mass General Brigham, Harvard Medical School, Boston, MA.
Ibrahim ChamseddineDepartment of Radiation Oncology, Mass General Brigham, Harvard Medical School, Boston, MA.ORCID 0000-0002-7005-8692

Funding

Project 3: Enhanced Sensitivity of Tumors to Proton Beam Therapy: Mechanisms and Biomarkers.P01CA261669 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI TITT, UWE · 2021 to 2025
$14.0M
NCI NIH HHS P01 CA261669
6 · The paper itself

Abstract

purposeFederated learning (FL) enables multi-institutional predictive modeling without sharing raw patient data, preserving privacy while leveraging diverse data sets. This study evaluates the use of linear FL (LFL) as an interpretable approach to enhance sample size and generalizability in outcome prediction. As a proof of concept, we applied LFL to patients with hepatocellular carcinoma (HCC) undergoing external beam radiotherapy (EBRT), predicting hepatic toxicity and 1-year survival (SRVy1).

methodsPatient data from Massachusetts General Hospital (MGH) and Brigham and Women's Hospital (BWH) were used to train models, whereas an independent validation data set from MD Anderson Cancer Center assessed generalizability. Logistic regression was developed to predict hepatic toxicity and SRVy1 using key clinical features, including baseline albumin, bilirubin, Child-Pugh score, liver size, and mean liver dose. The LFL approach allowed each institution to train models locally without sharing raw patient data. Model performance was evaluated using the AUC and compared between the LFL model and institution-specific models.

resultsFor survival prediction, single-institution models were limited, with AUC = 0.55-0.63, with LFL increasing it to 0.67. For toxicity prediction, external validation showed AUC = 0.68 for the MGH model and 0.69 for the BWH model, with LFL maintaining the AUC at 0.7. The model coefficients were moderate in the LFL compared with the single-institution models, indicating an ability to mitigate bias, which was also reflected by better performance on the validation data set.

conclusionLFL maintained or improved predictive performance over single-institution models for survival and hepatic toxicity in patients with HCC treated with EBRT while preserving model interpretability and patient privacy. These findings support LFL's role in multi-institutional collaborations.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAgedFederated LearningFemaleHumansMaleMiddle AgedPrognosisTreatment Outcome

Identifiers

PMID40587816
PMCPMC12319563

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