Development and external validation of a prediction model for overall survival after resection of distal cholangiocarcinoma

医学 一致性 队列 比例危险模型 内科学 阿卡克信息准则 多元分析 多元统计 癌症 外科 肿瘤科 胃肠病学 统计 数学
作者
Ali Belkouz,Stijn van Roessel,Marin Strijker,Jacob L. van Dam,Lois A. Daamen,Lydia G. van der Geest,Alberto Balduzzi,Andrea Benedetti Cacciaguerra,Susan van Dieren,Q. Molenaar,Bas Groot Koerkamp,Joanne Verheij,E. Van Eycken,Giuseppe Malleo,Mohammad Abu Hilal,Martijn G.H. van Oijen,Ivan Borbath,Chris Verslype,Cornelis J.A. Punt,Marc G. Besselink,Heinz‐Josef Klümpen
出处
期刊:British Journal of Cancer [Springer Nature]
卷期号:126 (9): 1280-1288 被引量:11
标识
DOI:10.1038/s41416-021-01687-1
摘要

Various prognostic factors are associated with overall survival (OS) after resection of distal cholangiocarcinoma (dCCA). The objective of this study was to develop and validate a prediction model for 3-year OS after pancreatoduodenectomy for dCCA.The derivation cohort consisted of all patients who underwent pancreatoduodenectomy for dCCA in the Netherlands (2009-2016). Clinically relevant variables were selected based on the Akaike information criterion using a multivariate Cox proportional hazards regression model, with model performance being assessed by concordance index (C-index) and calibration plots. External validation was performed using patients from the Belgium Cancer Registry (2008-2016), and patients from two university hospitals of Southampton (U.K.) and Verona (Italy).Independent prognostic factors for OS in the derivation cohort of 454 patients after pancreatoduodenectomy for dCCA were age (HR 1.02, 95% CI 1.01-1.03), pT (HR 1.43, 95% CI 1.07-1.90) and pN category (pN1: HR 1.78, 95% CI 1.37-2.32; pN2: HR 2.21, 95% CI 1.63-3.01), resection margin status (HR 1.79, 95% CI 1.39-2.29) and tumour differentiation (HR 2.02, 95% CI 1.62-2.53). The prediction model was based on these prognostic factors. The optimism-adjusted C-indices were similar in the derivation cohort (0.69), and in the Belgian (0.66) and Southampton-Verona (0.68) validation cohorts. Calibration was accurate in the Belgian validation cohort (slope = 0.93, intercept = 0.12), but slightly less optimal in the Southampton-Verona validation cohort (slope = 0.88, intercept = 0.32). Based on this model, three risk groups with different prognoses were identified (3-year OS of 65.4%, 33.2% and 11.8%).The prediction model for 3-year OS after resection of dCCA had reasonable performance in both the derivation and geographically external validation cohort. Calibration slightly differed between validation cohorts. The model is readily available via www. pancreascalculator.com to inform patients from Western European countries on their prognosis, and may be used to stratify patients for clinical trials.
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