4.5 Article

Development and validation of a prognostic nomogram for patients with stage II colon mucinous adenocarcinoma

期刊

INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
卷 37, 期 10, 页码 2173-2184

出版社

SPRINGER
DOI: 10.1007/s00384-022-04251-2

关键词

Colon cancer; Mucinous adenocarcinoma; Prognosis; Nomogram; Survival

资金

  1. Scientific Research Fund Project of Hunan Provincial Health Commission [20201919]
  2. Clinical Medical Technology Innovation Project of Hunan Province [2020SK51815]
  3. Natural Science Foundation of Hunan Province [2022JJ30538]

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The aim of this study was to establish an evaluation tool to accurately predict the survival of stage II C-MAC patients who underwent surgical treatment, and to identify a subgroup of patients who may benefit from chemotherapy.
Purpose Mucinous histology is generally considered as a risk factor of prognosis in stage II colon cancer, but there is no appropriate model for prognostic evaluation and treatment decision in patients with stage II colon mucinous adenocarcinoma (C-MAC) Thus, it is urgent to develop a comprehensive, individualized evaluation tool to reflect the heterogeneity of stage II C-MAC. Methods Patients with stage II C-MAC who underwent surgical treatment in the Surveillance, Epidemiology, and End Results Program were enrolled and randomly divided into training cohort (70%) and internal validation cohort (30%). Prognostic predictors which were determined by univariate and multivariate analysis in the training cohort were included in the nomogram. The calibration curves, decision curve analysis, X-tile analysis, and Kaplan-Meier curve of the nomogram were validated in the internal validation cohort. Results Three thousand seven hundred sixty-two patients of stage II C-MAC were enrolled. The age, pathological T (pT) stage, tumor number, serum carcinoembryonic antigen (CEA), and perineural invasion (PNI) were independent predictors of overall survival (OS), which were used to establish a nomogram. Calibration curves of the nomogram indicated good consistency between nomogram prediction and actual survival for 1-, 3- and 5-year OS. Besides, patients with stage II C-MAC could be divided into high-, middle-, and low-risk subgroups by the nomogram. Further subgroup analysis indicated that patients in the high-risk group could have a survival benefit from chemotherapy after surgical treatment. Conclusions We established the first nomogram to accurately predict the survival of stage II C-MAC patients who underwent surgical treatment. In addition, the nomogram identified low-, middle-, and high-risk subgroups of patients and found chemotherapy might improve survival in the high-risk subgroup of stage II C-MAC patients.

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