Evidence map›Paper›PMID 42303673›Full record

ArticleScientific reports2026

Fully automated CT-based quantitative body composition analysis for predicting survival in patients with HCC undergoing TACE: a dual-cohort study.

Krzysztof Bartnik, Belgutei Tsevegmed, Kamil Książek, Zuzanna Wojtczak, Przemysław Biecek

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In one paragraph

Article in Scientific reports, 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Krzysztof BartnikSecond Department of Radiology, Medical University of Warsaw, Banacha 1a St, Warsaw, 02-097, Poland.
Belgutei TsevegmedSecond Department of Radiology, Medical University of Warsaw, Banacha 1a St, Warsaw, 02-097, Poland.
Kamil KsiążekCentre for Credible Artificial Intelligence, Warsaw University of Technology, Warsaw, Poland.
Zuzanna WojtczakSecond Department of Radiology, Medical University of Warsaw, Banacha 1a St, Warsaw, 02-097, Poland. zuzanna.wojtczak@wum.edu.pl.
Przemysław BiecekCentre for Credible Artificial Intelligence, Warsaw University of Technology, Warsaw, Poland.

Funding

Narodowe Centrum Nauki 2025/56/C/NZ7/00276 (DEC-2025/56/C/NZ7/00276
6 · The paper itself

Abstract

Transarterial chemoembolization (TACE) is a standard treatment for patients with unresectable hepatocellular carcinoma (HCC), yet existing models provide limited individualized risk stratification. Automated CT-derived body composition analysis has emerged as an objective marker of patient physiological reserve, but its value in prognostication in TACE patients is insufficiently studied. Therefore, the aim of the study was to evaluate the prognostic value of a fully automated, open-source pipeline for CT-based body composition analysis in predicting overall survival (OS) in patients with HCC undergoing TACE. In this study, we used two independent cohorts of treatment-naive patients undergoing TACE: the WAW-TACE cohort (development; n = 230, OS: 28.6 months) and the HCC-TACE-Seg cohort (validation; n = 100, OS: 24.0 months). Skeletal muscle and fat metrics were extracted from pre-treatment CTs using a standardized deep learning pipeline and normalized by sex. Survival analyses were performed using Cox proportional hazards (CoxPH) models and random survival forests (RSF). Skeletal muscle density (SMD) at the L3 level was the strongest and independent predictor of OS across both cohorts (HR: development, 0.84; p = 0.029; validation, 0.79; p = 0.028). This association remained significant after adjustment for the best-performing clinical composite scores: mHAP-2 in the development (adjusted HR = 0.68; p = 0.049) and CLIP in the validation cohort (adjusted HR = 0.43; p = 0.003). In CoxPH, the addition of SMD metrics resulted in only modest improvements in discrimination (ΔC-index 0.011-0.037) that did not reach statistical significance. In contrast, RSF analysis demonstrated a statistically significant improvement in model discrimination when muscle-based variables were added to clinical features (ΔC-index = 0.023; p < 0.001). In both cohorts, SMD showed a reproducible independent prognostic association with overall survival. While adding SMD to traditional clinical models resulted in only modest, and in Cox-based analyses not statistically significant, improvements in discrimination, SMD provided complementary prognostic information. This suggests that the primary value of these automated CT-derived body composition metrics lies not in their performance as standalone predictors, but in their ability to provide an additional layer of objective biological data that may contribute to risk stratification in a complementary and exploratory manner within multivariable frameworks. Notably, in internally cross-validated RSF analyses, statistically significant increases in model discrimination were observed when muscle-based features were integrated into the model, highlighting their potential complementary value within machine learning frameworks.

Indexed as

Body CompositionCarcinoma, HepatocellularChemoembolization, TherapeuticLiver NeoplasmsTomography, X-Ray ComputedAgedCohort StudiesFemaleHumansMaleMiddle AgedMuscle, SkeletalPrognosisProportional Hazards ModelsSurvival Analysis

Identifiers

PMID42303673
PMCPMC13534685

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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 Socratic graph.