Evidence map›Paper›PMID 42871160›Full record

ArticleFrontiers in oncology2026

AI-assisted 3D thoracic body composition analysis identifies candidate imaging markers associated with overall survival in older patients with lung cancer receiving radiotherapy.

Saerom Sung, Hyun Joon Choi, Sangwoon Jeong, Wonyoung Cho, Yoon Jo Kim, Hyejung Cha, Chul Hee Min, Mi Sun Kim

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Article in Frontiers in oncology, 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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5 · Who and what money

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8 authors.

Saerom SungDepartment of Radiation Convergence Engineering, Yonsei University, Wonju, Republic of Korea.
Hyun Joon ChoiDepartment of Radiation Oncology, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Sangwoon JeongDepartment of Radiation Oncology, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Wonyoung ChoOncosoft Inc., Seoul, Republic of Korea.
Yoon Jo KimOncosoft Inc., Seoul, Republic of Korea.
Hyejung ChaDepartment of Radiation Oncology, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Chul Hee MinDepartment of Radiation Convergence Engineering, Yonsei University, Wonju, Republic of Korea.
Mi Sun KimDepartment of Radiation Oncology, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Older patients with lung cancer receiving thoracic radiotherapy have heterogeneous outcomes that are not fully captured by conventional clinical descriptors. We evaluated whether artificial intelligence (AI)-assisted three-dimensional (3D) thoracic body-composition analysis of pretreatment radiotherapy simulation computed tomography (CT) could identify candidate body-composition imaging markers associated with overall survival. Methods: This exploratory retrospective single-institution study included 88 patients aged 70 years or older who received thoracic radiotherapy for lung cancer between 2019 and 2021. Thoracic skeletal muscle and intermuscular fat were segmented using an AI-assisted workflow followed by expert review and Hounsfield unit-constrained refinement. Twelve knowledge-informed candidate groups were evaluated using conventional Cox regression. After marker selection, the selected marker pair was assessed in continuous form using bootstrap optimism correction, repeated five-fold cross-validation, and Uno's C-index. Penalized and alternative model-family analysis were performed as exploratory sensitivity analysis. Results: During follow-up, 28 deaths occurred. In an 18-case internal technical validation subset, the raw AI contours achieved Dice similarity coefficients of 0.930 for thoracic skeletal muscle and 0.723 for intermuscular fat. For Group 12, intermuscular adiposity index (IAI) and attenuation-weighted thoracic muscle fraction (TMF) were the variables that met the univariable screening criterion; the resulting two-marker model met the discrimination threshold without problematic collinearity. When modeled together, IAI values above the cohort median (hazard ratio [HR], 2.78; 95% confidence interval [CI], 1.25-6.18; P = 0.012) and TMF values above the cohort median (HR, 3.77; 95% CI, 1.52-9.32; P = 0.004) were associated with poorer overall survival. In continuous form, the selected marker pair had an optimism-corrected Harrell's C-index of 0.751 (95% CI, 0.661-0.849), a mean repeated cross-validation C-index of 0.753 ± 0.112, and Uno's C-index of 0.737. These performance estimates were conditional on prior marker selection. Conclusion: AI-assisted analysis of routine radiotherapy simulation CT identified IAI and TMF as candidate body-composition imaging markers associated with overall survival in this clinically heterogeneous cohort. The findings are exploratory and require independent evaluation in larger, clinically characterized cohorts before clinical use.

Indexed as

artificial intelligencebody compositionintermuscular fatlung cancerprognostic imaging markersradiotherapysimulation CTskeletal muscle

Identifiers

PMID42871160
PMCPMC13658111

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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.