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Development and validation of a CT-measured body composition radiomics model for prognostic assessment in resected pancreatic adenocarcinoma.

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Scientific reports 📖 저널 OA 98.8% 2021: 24/24 OA 2022: 32/32 OA 2023: 45/45 OA 2024: 140/140 OA 2025: 938/938 OA 2026: 743/767 OA 2021~2026 2025 Vol.15(1) p. 28722
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Gu Q, Liu P, Hu X, Liu J, He Y

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Pancreatic ductal adenocarcinoma (PDAC) carries a dismal prognosis due to high post-resection recurrence, yet current prognostic tools inadequately capture systemic tumor-host interactions.

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  • 표본수 (n) 142
  • p-value p < 0.001
  • HR 6.455

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↓ .bib ↓ .ris
APA Gu Q, Liu P, et al. (2025). Development and validation of a CT-measured body composition radiomics model for prognostic assessment in resected pancreatic adenocarcinoma.. Scientific reports, 15(1), 28722. https://doi.org/10.1038/s41598-025-14397-y
MLA Gu Q, et al.. "Development and validation of a CT-measured body composition radiomics model for prognostic assessment in resected pancreatic adenocarcinoma.." Scientific reports, vol. 15, no. 1, 2025, pp. 28722.
PMID 40770061 ↗

Abstract

Pancreatic ductal adenocarcinoma (PDAC) carries a dismal prognosis due to high post-resection recurrence, yet current prognostic tools inadequately capture systemic tumor-host interactions. This study developed and validated a novel CT-based body composition radiomics model for predicting recurrence-free survival (RFS) in 191 PDAC patients undergoing curative resection. Using a temporal validation design (training cohort: 2019-2022, n = 142; validation cohort: 2016-2018, n = 49), we extracted 1,688 radiomics features from adipose and muscle tissues at the L3 vertebral level. Following a standardized feature selection protocol (variance filtering, correlation reduction, and Cox regression), we constructed fat- and muscle-specific radiomics scores, combining them into a unified risk stratification system. The combined model effectively identified high-risk patients with significantly reduced RFS (HR = 6.455, p < 0.001), achieving consistent performance across cohorts (C-index: 0.71 training, 0.69 validation). This approach quantifies metabolic alterations in body composition, providing a clinically actionable tool to guide personalized therapy decisions-including intensified neoadjuvant regimens for high-risk patients or standard surveillance for low-risk individuals.

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