Predicting Risk of Colorectal Cancer After Adenoma Removal in a Large Community-Based Setting

Author:

Lee Jeffrey K.1,Jensen Christopher D.1ORCID,Udaltsova Natalia1ORCID,Zheng Yingye2ORCID,Levin Theodore R.1ORCID,Chubak Jessica3ORCID,Kamineni Aruna3ORCID,Halm Ethan A.4ORCID,Skinner Celette S.5,Schottinger Joanne E.6,Ghai Nirupa R.7,Burnett-Hartman Andrea8,Issaka Rachel2,Corley Douglas A.1

Affiliation:

1. Division of Research, Kaiser Permanente Northern California, Oakland, California, USA;

2. Fred Hutchinson Cancer Research Center, Seattle, Washington, USA;

3. Kaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, USA;

4. Rutgers Biological Health Sciences, Rutgers University, New Brunswick, New Jersey, USA;

5. Simmons Comprehensive Cancer Center and Department of Population & Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas, USA;

6. Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California, USA;

7. Department of Quality and Systems of Care, Kaiser Permanente Southern California, Pasadena, California, USA;

8. Kaiser Permanente Colorado, Institute for Health Research, Aurora, Colorado, USA.

Abstract

INTRODUCTION: Colonoscopy surveillance guidelines categorize individuals as high or low risk for future colorectal cancer (CRC) based primarily on their prior polyp characteristics, but this approach is imprecise, and consideration of other risk factors may improve postpolypectomy risk stratification. METHODS: Among patients who underwent a baseline colonoscopy with removal of a conventional adenoma in 2004–2016, we compared the performance for postpolypectomy CRC risk prediction (through 2020) of a comprehensive model featuring patient age, diabetes diagnosis, and baseline colonoscopy indication and prior polyp findings (i.e., adenoma with advanced histology, polyp size ≥10 mm, and sessile serrated adenoma or traditional serrated adenoma) with a polyp model featuring only polyp findings. Models were developed using Cox regression. Performance was assessed using area under the receiver operating characteristic curve (AUC) and calibration by the Hosmer-Lemeshow goodness-of-fit test. RESULTS: Among 95,001 patients randomly divided 70:30 into model development (n = 66,500) and internal validation cohorts (n = 28,501), 495 CRC were subsequently diagnosed; 354 in the development cohort and 141 in the validation cohort. Models demonstrated adequate calibration, and the comprehensive model demonstrated superior predictive performance to the polyp model in the development cohort (AUC 0.71, 95% confidence interval [CI] 0.68–0.74 vs AUC 0.61, 95% CI 0.58–0.64, respectively) and validation cohort (AUC 0.70, 95% CI 0.65–0.75 vs AUC 0.62, 95% CI 0.57–0.67, respectively). DISCUSSION: A comprehensive CRC risk prediction model featuring patient age, diabetes diagnosis, and baseline colonoscopy indication and polyp findings was more accurate at predicting postpolypectomy CRC diagnosis than a model based on polyp findings alone.

Funder

National Cancer Institute

Publisher

Ovid Technologies (Wolters Kluwer Health)

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