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Mortality from upper gastrointestinal tumors in colorectal cancer screening patients.
- Source :
-
Endoscopy international open [Endosc Int Open] 2024 Jul 25; Vol. 12 (7), pp. E916-E923. Date of Electronic Publication: 2024 Jul 25 (Print Publication: 2024). - Publication Year :
- 2024
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Abstract
- Background and study aims Currently, gastric cancer screening is only cost-effective in countries with high incidence. Integrated screening, in which gastroscopy is performed in conjunction with colonoscopy, could help reduce the gastric cancer screening procedure burden in countries with low or intermediate incidence. However, there is a lack of population-based studies to identify high-risk groups. Methods In this retrospective analysis of a colorectal cancer (CRC) screening program database, we used Cox proportional hazards model to identify an association of high- and low-risk finding (polyps ≥ 10 mm or with high-grade dysplasia) with time to death from upper gastrointestinal cancer (esophageal and gastric). We estimated the 10-year mortality of upper gastrointestinal tumors in different 10-year age groups, stratified by sex and polyp finding at colonoscopy. Results We included 349,856 CRC screening colonoscopies in our study. The median follow-up time was 5.22 years (95% confidence interval [CI] 5.21-5.24 years). Of the participants, 4.5% had polyps ≥ 10 mm or with high-grade dysplasia (HGD). At the end of the study period, 384 deaths from upper gastrointestinal cancer had occurred. Aside from age and sex, we found the presence of high-risk polyps to be significantly associated with upper gastrointestinal cancer death (hazard ratio 1.54, 95% CI 1.06-2.25, P = 0.025). Conclusions CRC screening participants with polyps < 10 mm and no HGD have a lower risk for mortality from upper gastrointestinal cancers compared with participants with polyps > 10 mm and HGD. Future studies will demonstrate whether integrated screening with additional gastroscopy is effective in CRC screening participants with large or highly dysplastic polyps.<br />Competing Interests: Conflict of Interest MT has advised for Abbvie, Albireo, BiomX, Boehringer Ingelheim, Falk, Gilead, Genfit, Hightide, Intercept, Jannsen, MSD, Novartis, Phenex, Pliant, Regulus, Siemens, and Shire, has received grants/research support from Albireo, Alnylam, Cymabay, Falk Pharma, Gilead, Intercept, MSD, Takeda, and UltraGenyx, has received speaker's fees form BMS, Falk Foundation, Gilead, Intercept, Madrigal, MSD and Roche, has received travel grants from AbbVie, Falk Foundation, Gilead, Intercept, Janssen and Roche, the Medical Universities of Graz and Vienna have filed patents on medical use of norUDCA and is listed as co-inventor. All other authors have no conflict of interest to declare.<br /> (The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).)
Details
- Language :
- English
- ISSN :
- 2364-3722
- Volume :
- 12
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Endoscopy international open
- Publication Type :
- Academic Journal
- Accession number :
- 39055263
- Full Text :
- https://doi.org/10.1055/a-2348-9264