% IMPORTANT: The following is UTF-8 encoded. This means that in the presence % of non-ASCII characters, it will not work with BibTeX 0.99 or older. % Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or % “biber”. @ARTICLE{Smith:141708, author = {T. Smith and D. C. Muller and K. G. M. Moons and A. J. Cross and M. Johansson and P. Ferrari and G. Fagherazzi and P. H. M. Peeters and G. Severi and A. Hüsing$^*$ and R. Kaaks$^*$ and A. Tjonneland and A. Olsen and K. Overvad and C. Bonet and M. Rodriguez-Barranco and J. M. Huerta and A. Barricarte Gurrea and K. E. Bradbury and A. Trichopoulou and C. Bamia and P. Orfanos and D. Palli and V. Pala and P. Vineis and B. Bueno-de-Mesquita and B. Ohlsson and S. Harlid and B. Van Guelpen and G. Skeie and E. Weiderpass and M. Jenab and N. Murphy and E. Riboli and M. J. Gunter and K. J. Aleksandrova and I. Tzoulaki}, title = {{C}omparison of prognostic models to predict the occurrence of colorectal cancer in asymptomatic individuals: a systematic literature review and external validation in the {EPIC} and {UK} {B}iobank prospective cohort studies.}, journal = {Gut}, volume = {68}, number = {4}, issn = {1468-3288}, address = {London}, publisher = {BMJ Publishing Group}, reportid = {DKFZ-2018-01979}, pages = {672-683}, year = {2019}, abstract = {To systematically identify and validate published colorectal cancer risk prediction models that do not require invasive testing in two large population-based prospective cohorts.Models were identified through an update of a published systematic review and validated in the European Prospective Investigation into Cancer and Nutrition (EPIC) and the UK Biobank. The performance of the models to predict the occurrence of colorectal cancer within 5 or 10 years after study enrolment was assessed by discrimination (C-statistic) and calibration (plots of observed vs predicted probability).The systematic review and its update identified 16 models from 8 publications (8 colorectal, 5 colon and 3 rectal). The number of participants included in each model validation ranged from 41 587 to 396 515, and the number of cases ranged from 115 to 1781. Eligible and ineligible participants across the models were largely comparable. Calibration of the models, where assessable, was very good and further improved by recalibration. The C-statistics of the models were largely similar between validation cohorts with the highest values achieved being 0.70 $(95\%$ CI 0.68 to 0.72) in the UK Biobank and 0.71 $(95\%$ CI 0.67 to 0.74) in EPIC.Several of these non-invasive models exhibited good calibration and discrimination within both external validation populations and are therefore potentially suitable candidates for the facilitation of risk stratification in population-based colorectal screening programmes. Future work should both evaluate this potential, through modelling and impact studies, and ascertain if further enhancement in their performance can be obtained.}, subtyp = {Review Article}, cin = {C020}, ddc = {610}, cid = {I:(DE-He78)C020-20160331}, pnm = {313 - Cancer risk factors and prevention (POF3-313)}, pid = {G:(DE-HGF)POF3-313}, typ = {PUB:(DE-HGF)16}, pubmed = {pmid:29615487}, doi = {10.1136/gutjnl-2017-315730}, url = {https://inrepo02.dkfz.de/record/141708}, }