Kim et al. 8 also suggested that young age and right-side location were independent factors associated with interval cancer in a multivariate analysis. In a recent study from Canada, however, female sex, older age, and performance of the colonoscopy by a non-gastroenterologist were identified as predictors of interval cancers after a negative colonoscopy.
3,4Although other authors suggested the accelerated tumor biology in young patients as a cause of interval cancer, the authors of the Canadian studies 3,4 suggested that a deficiency in the quality of colonoscopic data rather than accelerated tumor biology was the cause of most of the interval cancers occurring after a negative colonoscopy. Furthermore, information on family CRC history or hereditary syndromes was not described by Kim et al.; therefore, their study might have been unable to evaluate the age impact on interval cancers, as young age in familial CRC may have a confounding effect on the interval cancer. As pointed out by the authors, it would be better if quality colonoscopic data such as bowel preparation, completeness, and adenoma detection rate, as well as qualifications of endoscopists, were assessed as predictors of the occurrence of interval cancers. Considering the wide variation in the detection rates of adenomas and serrated polyps between endoscopists, the quality of colonoscopic data should be stressed and assessed as a predictor of interval cancers. However, to answer these questions, a population-based cohort design with complete follow-up might be warranted.While we applaud the investigators for obtaining Korean