Evidence map›Paper›PMID 42008048›Full record

ArticleInsights into imaging2026

Decoding the association between CT-derived body composition metrics and prognosis in stage II rectal cancer.

Fengli Jiang, Ziyan Weng, Zhiqing Shao, Qianling Li, Jie Lin, Dening Ma, Xinyi Gao

Abstract read
In one paragraph

Article in Insights into imaging, 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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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Fengli Jiang *Department of Radiology, Zhejiang Cancer Hospital, 310022, Hangzhou, Zhejiang, China.
Ziyan Weng *Postgraduate training base Alliance of Wenzhou Medical University (Zhejiang Cancer Hospital), 310022, Hangzhou, Zhejiang Province, China.
Zhiqing ShaoDepartment of Radiology, Zhejiang Cancer Hospital, 310022, Hangzhou, Zhejiang, China.
Qianling LiDepartment of Radiology, Zhejiang Cancer Hospital, 310022, Hangzhou, Zhejiang, China.
Jie LinDepartment of Radiology, Zhejiang Cancer Hospital, 310022, Hangzhou, Zhejiang, China.
Dening MaPostgraduate training base Alliance of Wenzhou Medical University (Zhejiang Cancer Hospital), 310022, Hangzhou, Zhejiang Province, China. madeningsdu@163.com.
Xinyi GaoDepartment of Radiology, Zhejiang Cancer Hospital, 310022, Hangzhou, Zhejiang, China. 10301010213@fudan.edu.cn.ORCID http://orcid.org/0000-0002-3678-1182

Funding

Medical Health Science and Technology Project of Zhejiang Province 2022KY628Natural Science Foundation of Zhejiang Province LQN25H180004Zhejiang Province Traditional Chinese Medicine Science and Technology Project 2024ZL327
6 · The paper itself

Abstract

objectivesTo evaluate the prognostic impact of CT-derived body composition metrics and clinical factors, and to develop a prognostic model in patients with stage II rectal cancer. MATERIALS AND

methodsThis retrospective study analyzed consecutive stage II rectal cancer patients who underwent radical surgery. The predictive value of body composition metrics and clinical factors was evaluated. A Cox proportional hazards model-derived nomogram, based on independent risk factors identified through univariate and multivariate analyses, was established and validated to predict overall survival (OS).

resultsAmong 975 patients (median age 63 years, IQR 55-70 years; 644 [66.1%] males), 183 deaths were recorded during a median follow-up period of 53 months (IQR 33-83 months). Low skeletal muscle density (SMD) (OR = 0.43; 95% CI: 0.20, 0.91), age ≥ 65 years, and CA125 positive (p < 0.05) were risk factors for severe postoperative complications. High visceral-to-subcutaneous adipose ratio (VSR) (OR = 1.33; 95% CI: 1.02, 1.73), body mass index (BMI) > 24.9, and T4 stage (p < 0.05) were risk factors for prolonged hospitalization. After univariate and multivariate analyses, the nomogram based on age, gross type, perineural invasion, lymphovascular invasion, inflammatory burden index, subcutaneous fat area (SFA), and SMD (p < 0.05) exhibited area under the curve values of 0.77/0.62, 0.77/0.62, and 0.75/0.67 at 1-year, 3-year, and 5-year OS in training/validation sets, respectively.

conclusionsIn predicting the prognosis of stage II rectal cancer patients, VSR, SFA, and SMD were superior to other body composition metrics. The nomogram integrating body composition metrics and clinical factors showed superior predictive performance for OS compared to a single risk factor alone. CRITICAL RELEVANCE STATEMENT: CT-derived body composition metrics can predict the prognosis of rectal cancer patients by reflecting the nutritional and metabolic status. KEY POINTS: Body composition metrics' prognostic utility in stage II rectal cancer is clear. Body composition metrics are associated with clinical outcomes in stage II rectal cancer. Body composition is a predictive biomarker for stage II rectal cancer.

Indexed as

Body composition metricsComputed tomographyPrognosisStage II rectal cancer

Identifiers

PMID42008048
PMCPMC13096300

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