Multitarget Stool DNA Test Performance in an Average-Risk Colorectal Cancer Screening Population

Autor: Linda J.W. Bosch, Kathleen L.J. Daenen, Gerrit A. Meijer, Barry M. Berger, Michael J. Domanico, S.T. van Turenhout, Veerle M.H. Coupé, Sandra Mongera, Cjj Mulder, Graham P. Lidgard, E. Dekker, Esther M. Stoop, T. R. de Wijkerslooth, M. van Engeland, Beatriz Carvalho, Ernst J. Kuipers, Christian Rausch, Veerle Melotte
Přispěvatelé: Gastroenterology & Hepatology, Gastroenterology and Hepatology, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, APH - Quality of Care, AGEM - Re-generation and cancer of the digestive system, Pathology, CCA - Imaging and biomarkers, Epidemiology and Data Science, APH - Methodology, Pathologie, RS: GROW - R2 - Basic and Translational Cancer Biology, RS: GROW - School for Oncology and Reproduction
Rok vydání: 2019
Předmět:
Zdroj: American Journal of Gastroenterology, 114(12), 1909-1918. Springer Nature
The American Journal of Gastroenterology
American journal of gastroenterology, 114(12), 1909-1918. Springer Nature
American Journal of Gastroenterology, 114(12), 1909-1918. Nature Publishing Group
Bosch, L J W, Melotte, V, Mongera, S, Daenen, K L J, Coupé, V M H, van Turenhout, S T, Stoop, E M, de Wijkerslooth, T R, Mulder, C J J, Rausch, C, Kuipers, E J, Dekker, E, Domanico, M J, Lidgard, G P, Berger, B M, van Engeland, M, Carvalho, B & Meijer, G A 2019, ' Multitarget Stool DNA Test Performance in an Average-Risk Colorectal Cancer Screening Population ', American Journal of Gastroenterology, vol. 114, no. 12, pp. 1909-1918 . https://doi.org/10.14309/ajg.0000000000000445
ISSN: 0002-9270
DOI: 10.14309/ajg.0000000000000445
Popis: INTRODUCTION: We set out to evaluate the performance of a multitarget stool DNA (MT-sDNA) in an average-risk colonoscopy-controlled colorectal cancer (CRC) screening population. MT-sDNA stool test results were evaluated against fecal immunochemical test (FIT) results for the detection of different lesions, including molecularly defined high-risk adenomas and several other tumor characteristics.METHODS: Whole stool samples (n = 1,047) were prospectively collected and subjected to an MT-sDNA test, which tests for KRAS mutations, NDRG4 and BMP3 promoter methylation, and hemoglobin. Results for detecting CRC (n = 7), advanced precancerous lesions (advanced adenoma [AA] and advanced serrated polyps; n = 119), and non-AAs (n = 191) were compared with those of FIT alone (thresholds of 50, 75, and 100 hemoglobin/mL). AAs with high risk of progression were defined by the presence of specific DNA copy number events as measured by low-pass whole genome sequencing.RESULTS: The MT-sDNA test was more sensitive than FIT alone in detecting advanced precancerous lesions (46% (55/119) vs 27% (32/119), respectively, PDISCUSSION: In an average-risk screening population, the MT-sDNA test has an increased sensitivity for detecting advanced precancerous lesions compared with FIT alone. AAs with a high risk of progression were not detected with significantly higher sensitivity by MT-sDNA or FIT.
Databáze: OpenAIRE