Evidence map›Paper›PMID 40310642›Full record

ArticleJAMA network open2025

Deep Learning Model of Primary Tumor and Metastatic Cervical Lymph Nodes From CT for Outcome Predictions in Oropharyngeal Cancer.

Bolin Song, Amaury Leroy, Kailin Yang, Sirvan Khalighi, Krunal Pandav, Tanmoy Dam, Jonathan Lee, Sarah Stock, Xiao T Li, Jay Sonuga and 5 more

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
–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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

15 authors.

Bolin SongWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia.
Amaury LeroyTherapanacea, Paris, France.
Kailin YangDepartment of Radiation Oncology, Holden Comprehensive Cancer Center, Iowa Neuroscience Institute, University of Iowa, Iowa City.
Sirvan KhalighiWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia.
Krunal PandavWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia.
Tanmoy DamWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia.
Jonathan LeeDiagnostics Institute, Cleveland Clinic, Cleveland, Ohio.
Sarah StockDiagnostics Institute, Cleveland Clinic, Cleveland, Ohio.
Xiao T LiDepartment of Radiology and Imaging Sciences, Emory University Hospital, Atlanta, Georgia.
Jay SonugaWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia.
Pingfu FuDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, Ohio.
Shlomo KoyfmanDepartment of Radiation Oncology, Holden Comprehensive Cancer Center, Iowa Neuroscience Institute, University of Iowa, Iowa City.
Nabil F SabaDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Atlanta, Georgia.
Mihir R PatelDepartment of Otolaryngology, Winship Cancer Institute, Atlanta, Georgia.
Anant MadabhushiWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia.

Funding

Pathology CoreU54CA254566 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MADABHUSHI, ANANT · 2020 to 2024
$5.0M
Computer-Assisted Histologic Evaluation of Cardiac Allograft RejectionR01HL151277 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MADABHUSHI, ANANT, MARGULIES, KENNETH BER · 2020 to 2023
$3.2M
Oral Cavity Quantitative Histomorphometric Risk Classifier (OHbIC) in Oral Cavity Squamous Cell Carcinoma (OC-SCC)R01CA249992 · NCI · EMORY UNIVERSITY · PI LEWIS, JAMES, MADABHUSHI, ANANT · 2021 to 2025
$3.2M
Computerized histologic image predictor of cancer outcomeR01CA202752 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI FELDMAN, MICHAEL D, GANESAN, SHRIDAR · 2016 to 2020
$3.1M
Prostate cancer risk stratification via computational 3D pathologyR01CA268207 · NCI · UNIVERSITY OF WASHINGTON · PI Jonathan T.C. Liu, Anant Madabhushi · 2022 to 2026
$3.1M
Quantitative Histomorphometric Risk Classifier (QuHbIC) in HPV + Oropharyngeal CarcinomaR01CA220581 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KOYFMAN, SHLOMO, LEWIS, JAMES · 2018 to 2023
$3.1M
Computerized Histologic Risk Predictor (CHiRP) for Early Stage Lung CancersR01CA216579 · NCI · EMORY UNIVERSITY · PI FU, PINGFU, LLOYD, MARK · 2018 to 2023
$3.1M
Prognostic and Predictive Digital Tissue Image Assay for Prostate CancerR01CA268287 · NCI · EMORY UNIVERSITY · PI GUPTA, SHILPA, LAL, PRITI · 2022 to 2025
$3.0M
MR Fingerprinting and Computerized Decision Support for Prostate CancerR01CA208236 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GULANI, VIKAS, PONSKY, LEE EVAN · 2017 to 2022
$3.0M
RADIOMIC APPROACHES TO IMPROVE TARGETING FOR ATRIAL FIBRILLATION CATHETER ABLATIONR01HL158071 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BARNARD, JOHN, CHUNG, MINA KAY · 2021 to 2024
$2.9M
Novel Radiomics for Predicting Response to Immunotherapy for Lung CancerR01CA257612 · NCI · EMORY UNIVERSITY · PI Anant Madabhushi, Vamsidhar Velcheti · 2021 to 2026
$2.7M
An AI-enabled Digital Pathology Platform for Multi-Cancer Diagnosis, Prognosis and Prediction of Therapeutic BenefitU01CA269181 · NCI · EMORY UNIVERSITY · PI Anant Madabhushi, tanuja shet · 2022 to 2026
$2.5M
BLRD VA IK6 BX006185NCI NIH HHS R01 CA202752NCI NIH HHS R01 CA208236NCI NIH HHS R01 CA216579NCI NIH HHS R01 CA220581NCI NIH HHS R01 CA249992NCI NIH HHS R01 CA257612NCI NIH HHS R01 CA268207NCI NIH HHS R01 CA268287NCI NIH HHS U01 CA239055NCI NIH HHS U01 CA248226NCI NIH HHS U01 CA269181NCI NIH HHS U54 CA254566NHLBI NIH HHS R01 HL151277NHLBI NIH HHS R01 HL158071NIBIB NIH HHS R43 EB028736
6 · The paper itself

Abstract

Importance: Primary tumor (PT) and metastatic cervical lymph node (LN) characteristics are highly associated with oropharyngeal squamous cell carcinoma (OPSCC) prognosis. Currently, there is a lack of studies to combine imaging characteristics of both regions for predictions of p16+ OPSCC outcomes. Objectives: To develop and validate a computed tomography (CT)-based deep learning classifier that integrates PT and LN features to predict outcomes in p16+ OPSCC and to identify patients with stage I disease who may derive added benefit associated with chemotherapy. Design, Setting, and Participants: In this retrospective prognostic study, radiographic CT scans were analyzed of 811 patients with p16+ OPSCC treated with definitive radiotherapy or chemoradiotherapy from 3 independent cohorts. One cohort from the Cancer Imaging Archive (1998-2013) was used for model development and validation and the 2 remaining cohorts (2002-2015) were used to externally test the model performance. The Swin Transformer architecture was applied to fuse the features from both PT and LN into a multiregion imaging risk score (SwinScore) to predict survival outcomes across and within subpopulations at various stages. Data analysis was performed between February and July 2024. Exposures: Definitive radiotherapy or chemoradiotherapy treatment for patients with p16+ OPSCC. Main Outcomes and Measures: Hazard ratios (HRs), log-rank tests, concordance index (C index), and net benefit were used to evaluate the associations between multiregion imaging risk score and disease-free survival (DFS), overall survival (OS), and locoregional failure (LRF). Interaction tests were conducted to assess whether the association of chemotherapy with outcome significantly differs across dichotomized multiregion imaging risk score subgroups. Results: The total patient cohort comprised 811 patients with p16+ OPSCC (median age, 59.0 years [IQR, 47.4-70.6 years]; 683 men [84.2%]). In the external test set, the multiregion imaging risk score was found to be prognostic of DFS (HR, 3.76 [95% CI, 1.99-7.10]; P < .001), OS (HR, 4.80 [95% CI, 2.22-10.40]; P < .001), and LRF (HR, 4.47 [95% CI, 1.43-14.00]; P = .01) among all patients with p16+ OPSCC. The multiregion imaging risk score, integrating both PT and LN information, demonstrated a higher C index (0.63) compared with models focusing solely on PT (0.61) or LN (0.58). Chemotherapy was associated with improved DFS only among patients with high scores (HR, 0.09 [95% CI, 0.02-0.47]; P = .004) but not those with low scores (HR, 0.83 [95% CI, 0.32-2.10]; P = .69). Conclusions and Relevance: This prognostic study of p16+ OPSCC describes the development of a CT-based imaging risk score integrating PT and metastatic cervical LN features to predict recurrence risk and identify suitable candidates for treatment tailoring. This tool could optimize treatment modulations of p16+ OPSCC at a highly granular level.

Indexed as

Deep LearningLymphatic MetastasisLymph NodesOropharyngeal NeoplasmsTomography, X-Ray ComputedAgedChemoradiotherapyFemaleHumansMaleMiddle AgedNeckPrognosisRetrospective Studies

Identifiers

PMID40310642
PMCPMC12046429

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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.