Evidence map›Paper›PMID 41987576›Full record

ArticleJNCI cancer spectrum2026

Contrastive multimodal deep learning for survival prediction in grade 2/3 gliomas.

Peiying Hua, Chun-Chieh Lin, Travis Fenlon, Xiaoying Liu, Saeed Hassanpour

Abstract read
In one paragraph

Article in JNCI cancer spectrum, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

5 authors.

Peiying HuaDepartment of Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, NH, United States.ORCID 0000-0002-4550-4144
Chun-Chieh LinDepartment of Pathology and Laboratory Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH, United States.ORCID 0000-0001-9679-4287
Travis FenlonDepartment of Pathology and Laboratory Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH, United States.
Xiaoying LiuDepartment of Pathology and Laboratory Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH, United States.
Saeed HassanpourDepartment of Biomedical Data Science, Geisel School of Medicine at Dartmouth, Hanover, NH, United States.ORCID 0000-0001-9460-6414

Funding

Advancing Digital Pathology through Novel Machine Learning MethodologiesR01LM013833 · NLM · DARTMOUTH COLLEGE · PI Saeed Hassanpour · 2022 to 2026
$3.0M
NLM NIH HHS R01 LM013833US National Library of Medicine R01LM013833
6 · The paper itself

Abstract

backgroundAccurate survival prediction for grade 2/3 glioma patients remains challenging due to tumor biological heterogeneity and limitations of current prognostic methods that rely on single-modality data.

methodsWe developed a multimodal deep learning framework integrating histopathology whole-slide images, somatic mutations, and clinical-demographic data. A 3-stage training pipeline combined contrastive learning with survival-specific optimization to align cross-modal representations. The framework was trained on 498 grade 2/3 glioma patients from The Cancer Genome Atlas and evaluated using 5-fold cross-validation and an independent Dartmouth-Hitchcock Medical Center (DHMC) cohort (n = 61).

resultsThe contrastive multimodal model achieved a c-index of 0.91 (95% confidence interval [CI] = 0.84 to 0.96), significantly outperforming the unimodal models (image-only = 0.76; non-image-only = 0.87) and showing an improvement over the noncontrastive multimodal model (c-index = 0.89), although this difference was not statistically significant. Kaplan-Meier analysis demonstrated clear survival separation across risk strata (log-rank P = 4.4 × 10-5). Contrastive learning improved representation clustering quality, with silhouette scores increasing from 0.20 to 0.24 (P = .05). External evaluation on the DHMC cohort achieved a c-index of 0.87 (95% CI = 0.77 to 0.95) after domain adaptation.

conclusionContrastive multimodal learning significantly enhances survival prediction in grade 2/3 gliomas by effectively integrating histopathology, genomics, and clinical data. This annotation-free approach enables early risk stratification using routinely collected data and shows promise for informing personalized treatment decisions and clinical trial stratification.

Indexed as

Brain NeoplasmsDeep LearningGliomaAdultAgedFemaleHumansKaplan-Meier EstimateMaleMiddle AgedMutationNeoplasm GradingPrognosis

Identifiers

PMID41987576
PMCPMC13199061

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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.