Trends in the incidence of young-onset colorectal cancer with a focus on years approaching screening age: A population-based longitudinal study

Author:

Howren Alyssa123,Sayre Eric C3,Loree Jonathan M45,Gill Sharlene45,Brown Carl J67,Raval Manoj J67,Farooq Ameer7,De Vera Mary A123

Affiliation:

1. University of British Columbia, Faculty of Pharmaceutical Sciences, 2405 Wesbrook Mall, Vancouver, BC Canada V6T 1Z3, Canada

2. Collaboration for Outcomes Research and Evaluation, 2405 Wesbrook Mall, Vancouver, BC Canada V6T 1Z3, Canada

3. Arthritis Research Canada, 5591 No 3 Rd, Richmond, BC V6X 2C7, Canada

4. University of British Columbia, Faculty of Medicine, Department of Medicine, Division of Medical Oncology, 2775 Laurel Street, 11th Floor, Vancouver, BC, V5Z 1M9, Canada

5. BC Cancer, 600 W 10th Ave, Vancouver, BC V5Z 4E6, Canada

6. University of British Columbia, Faculty of Medicine, Department of Surgery, 2775 Laurel Street, 11th Floor, Vancouver, BC, V5Z 1M9, Canada

7. St. Paul’s Hospital, 1081 Burrard St, Vancouver, BC V6Z 1Y6, Canada

Abstract

Abstract Background With recent evidence for the increasing risk of young-onset colorectal cancer (yCRC), our objective was to evaluate the incidence of yCRC in one-year age increments, particularly focusing around the screening age of 50 years. Methods We conducted a longitudinal study using linked administrative health databases in British Columbia, Canada including a provincial cancer registry, inpatient/outpatient visits, and vital statistics from January 1, 1986 to December 31, 2016. We calculated incidence rates per 100,000 at every age from 20 to 60 years and estimated annual percent change in incidence (APCi) of yCRC using joinpoint regression analysis. Results We identified 3,614 individuals with yCRC (49.9% women). The incidence of CRC steadily rose from 20 to 60 years, with a marked increase from 49 to 50 years (incidence rate ratio = 1.19; 95% confidence interval [CI] = 1.04 to 1.34). Furthermore, there was a trend of increased incidence of yCRC among women (APCi = 0.79%; 95% CI = 0.22% to 1.36%) and men (APCi = 2.17%; 95% CI = 1.59% to 2.76%). Analyses stratified by age yielded APCi’s of 2.49% (95% CI = 1.36% to 3.63%) and 0.12% (95% CI = -0.54% to 0.79%) for women aged 30-39 years and 40-49 years, respectively and 2.97% (95% CI = 1.65% to 4.31%) and 1.86% (95% CI = 1.19% to 2.53%) for men. Conclusion Our findings indicate a steady increase over one-year age increments in the risk of yCRC during the years approaching and beyond screening age. These findings highlight the need to raise awareness as well as continue discussions regarding considerations of lowering the screening age.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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