Evidence map›Paper›PMID 42787516›Full record

ArticleImmuno-oncology technology2026

A multimodal AI biomarker PATH-ORACLE improves prediction of recurrence in stage I lung adenocarcinoma.

O Kilim, O Pipek, Z Sztupinszki, M Diossy, A Prosz, C Naceur-Lombardelli, S Veeriah, D Moore, M Jamal-Hanjani, A Hackshaw and 5 more

Abstract read
In one paragraph

Article in Immuno-oncology technology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

O KilimDepartment of Physics of Complex Systems, Eötvös Loránd University, Budapest, Hungary.
O PipekDepartment of Physics of Complex Systems, Eötvös Loránd University, Budapest, Hungary.
Z SztupinszkiComputational Health Informatics Program, Boston Children's Hospital, Harvard Medical School, Boston, USA.
M DiossyComputational Health Informatics Program, Boston Children's Hospital, Harvard Medical School, Boston, USA.
A ProszTranslational Cancer Genomics Group, Danish Cancer Institute, Copenhagen, Denmark.
C Naceur-LombardelliCancer Research Institute, University College London Cancer Institute, London, UK.
S VeeriahCancer Research Institute, University College London Cancer Institute, London, UK.
D MooreCancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK.
M Jamal-HanjaniCancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.
A HackshawCancer Research UK & UCL Cancer Trials Centre, London, UK.
J FillingerDepartment of Pathology, National Korányi Institute of Pulmonology, Budapest, Hungary.
J MoldvayFirst Department of Pulmonology, National Korányi Institute of Pulmonology, Budapest, Hungary.
I CsabaiDepartment of Physics of Complex Systems, Eötvös Loránd University, Budapest, Hungary.
C SwantonCancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, UK.
Z SzallasiComputational Health Informatics Program, Boston Children's Hospital, Harvard Medical School, Boston, USA.

Funding

The Impact of DNA Damage Repair Abnormalities in Prostate CancerP01CA228696 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SOLIT, DAVID B. · 2019 to 2024
$8.7M
NCI NIH HHS P01 CA228696Wellcome Trust CC2041
6 · The paper itself

Abstract

Background: Surgical resection is the standard treatment for stage I lung adenocarcinoma, in most cases without additional systemic adjuvant treatment. A substantial proportion of stage I cases recur, with a 5-year survival rate <50%. Clinical data suggest that adjuvant treatment, including immune checkpoint inhibitor therapy, may improve survival in such recurrent cases. Previously evaluated predictors, including the International Association for the Study of Lung Cancer (IASLC) grading system applied to histological sections and transcriptomic profiles, have not been sufficiently accurate or consistent for risk stratification or to guide therapeutic intervention. We hypothesized that these diverse diagnostic measurements carry complementary information that may provide higher prognostic power when combined. Materials and methods: We developed PATH-ORACLE, a multimodal deep learning biomarker built on top of the prospectively validated transcriptomic-based Outcome Risk Associated Clonal Lung Expression (ORACLE) score, with the addition of routine histological sections processed by pretrained foundation models. Predictive performance was assessed in two independent cohorts. Results: The histology-only predictor outperformed automated IASLC grading and remained prognostic after adjustment for tumor size, grade and T-stage. PATH-ORACLE exceeded both constituent modalities, predicting 1-year recurrence with an area under the curve of 0.86 and 0.84 in the two independent validation cohorts, and separated high- and low-risk groups using a single prespecified cut-off. Conclusions: Extensive validation will be needed to convert PATH-ORACLE from a prognostic biomarker to a predictive biomarker that could be used to prioritize stage IB patients for adjuvant targeted therapy, chemotherapy, or immune checkpoint inhibitor therapy with or without liquid biopsy-based monitoring.

Indexed as

early-stage lung adenocarcinomamultimodal deep learningrecurrence prediction

Identifiers

PMID42787516
PMCPMC13602146

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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.