Evidence map›Paper›PMID 42204461›Full record

ArticleBMC gastroenterology2026

Prognostic value of CT-defined sarcopenic obesity in hepatocellular carcinoma patients undergoing transarterial chemoembolization.

Settawit Chatsuntiprapa, Kittipitch Bannangkoon, Teeravut Tubtawee, Natee Ina

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Article in BMC gastroenterology, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Settawit ChatsuntiprapaDepartment of Radiology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand.
Kittipitch BannangkoonDepartment of Radiology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand. drkittipitch@gmail.com.
Teeravut TubtaweeDepartment of Radiology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand.
Natee InaDepartment of Radiology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, 90110, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe prognostic value of sarcopenic obesity is controversial in hepatocellular carcinoma (HCC) patients undergoing transarterial chemoembolization (TACE). This study aimed to deconstruct the sarcopenic obesity phenotype to clarify the independent prognostic impacts of sarcopenia and visceral obesity.

methodsWe retrospectively analyzed 415 patients with unresectable HCC who underwent TACE between 2009 and 2020. Skeletal muscle index (SMI) and visceral fat area (VFA) were measured from baseline CT scans at the L3 vertebra level. Sarcopenia (SMI ≤ 36.2 cm²/m² in males, ≤ 29.6 cm²/m² in females) and visceral obesity (VFA ≥ 100 cm²) were defined using Asian-specific cutoffs. Overall survival (OS) was analyzed using Kaplan-Meier and Cox proportional hazards models, with sex-stratified analysis.

resultsAmong 415 patients (72% male, median follow-up 21.4 months), sarcopenia prevalence was 34% and visceral obesity 59%. In sex-stratified analysis, sarcopenia predicted mortality in males and reduced the median OS by 11 months (14.4 vs. 25.4 months, p < 0.001), but not in females (23.4 vs. 22.8 months, p = 0.900). Visceral obesity showed no prognostic impact in either sex. In sex-stratified multivariate analysis adjusting for Child-Pugh class, tumor burden, BCLC stage, and AFP, sarcopenia remained independently associated with mortality in males (adjusted hazard ratio [HR] = 1.41, 95% CI: 1.06-1.86, p = 0.018) but not in females (adjusted HR = 0.84, 95% CI: 0.55-1.27, p = 0.404; p for interaction = 0.070), while visceral obesity and sarcopenic obesity composite showed no prognostic value in either sex.

conclusionThe sarcopenic obesity composite phenotype lacks prognostic value in TACE-treated HCC patients. Sarcopenia independently predicts mortality in males but not females, while visceral obesity shows no independent prognostic significance. Clinical risk stratification could consider sarcopenia assessment in male patients rather than composite phenotypes.

Indexed as

Carcinoma, HepatocellularChemoembolization, TherapeuticLiver NeoplasmsObesity, AbdominalSarcopeniaAgedFemaleHumansIntra-Abdominal FatKaplan-Meier EstimateMaleMiddle AgedMuscle, SkeletalObesityPrognosisProportional Hazards ModelsBody CompositionHepatocellular CarcinomaSarcopeniaSkeletal Muscle IndexTransarterial ChemoembolizationVisceral Obesity

Identifiers

PMID42204461
PMCPMC13397963

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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.