<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cercek A</submitter><funding>Precision, Interception and Prevention Program at MSK</funding><funding>Romeo Milio Lynch Syndrome Foundation</funding><funding>Cancer is a program of the Entertainment Industry Foundation administered by the American Association for Cancer Research</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>Stand Up to Cancer Colorectal Cancer Dream Team Translational Research</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><funding>Marie-Josée and Henry R. Kravis Center for Molecular Oncology</funding><pagination>1683-1692</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8634406</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>113(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The causative factors for the recent increase in early-onset colorectal cancer (EO-CRC) incidence are unknown. We sought to determine if early-onset disease is clinically or genomically distinct from average-onset colorectal cancer (AO-CRC).&lt;h4>Methods&lt;/h4>Clinical, histopathologic, and genomic characteristics of EO-CRC patients (2014-2019), divided into age 35 years and younger and 36-49 years at diagnosis, were compared with AO-CRC (50 years and older). Patients with mismatch repair deficient tumors, CRC-related hereditary syndromes, and inflammatory bowel disease were excluded from all but the germline analysis. All statistical tests were 2-sided.&lt;h4>Results&lt;/h4>In total, 759 patients with EO-CRC (35 years, n = 151; 36-49 years, n = 608) and AO-CRC (n = 687) were incl</pubmed_abstract><journal>Journal of the National Cancer Institute</journal><pubmed_title>A Comprehensive Comparison of Early-Onset and Average-Onset Colorectal Cancers.</pubmed_title><pmcid>PMC8634406</pmcid><funding_grant_id>R25 CA233208</funding_grant_id><funding_grant_id>SU2C-AACR-DT22-17</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>K08 CA230213</funding_grant_id><funding_grant_id>T32 GM132083</funding_grant_id><funding_grant_id>T32 GM132083; R25 CA233208</funding_grant_id><pubmed_authors>Bandlamudi C</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Markowitz A</pubmed_authors><pubmed_authors>Birsoy O</pubmed_authors><pubmed_authors>Offit K</pubmed_authors><pubmed_authors>Robson M</pubmed_authors><pubmed_authors>Solit D</pubmed_authors><pubmed_authors>Joseph V</pubmed_authors><pubmed_authors>Varghese A</pubmed_authors><pubmed_authors>Reidy-Lagunes D</pubmed_authors><pubmed_authors>Yaeger R</pubmed_authors><pubmed_authors>Galle J</pubmed_authors><pubmed_authors>Guillem J</pubmed_authors><pubmed_authors>Diaz LA</pubmed_authors><pubmed_authors>Cercek A</pubmed_authors><pubmed_authors>Smith JJ</pubmed_authors><pubmed_authors>Maio A</pubmed_authors><pubmed_authors>Schultz N</pubmed_authors><pubmed_authors>Segal N</pubmed_authors><pubmed_authors>Srinivasan P</pubmed_authors><pubmed_authors>Taylor B</pubmed_authors><pubmed_authors>Kemeny N</pubmed_authors><pubmed_authors>Ganesh K</pubmed_authors><pubmed_authors>Mendelsohn R</pubmed_authors><pubmed_authors>Stadler ZK</pubmed_authors><pubmed_authors>Mandelker D</pubmed_authors><pubmed_authors>Belanfanti K</pubmed_authors><pubmed_authors>Aguilar JG</pubmed_authors><pubmed_authors>Lumish MA</pubmed_authors><pubmed_authors>Nash G</pubmed_authors><pubmed_authors>Walch H</pubmed_authors><pubmed_authors>Fernandes GDS</pubmed_authors><pubmed_authors>Tejada PR</pubmed_authors><pubmed_authors>Paty PB</pubmed_authors><pubmed_authors>Kemel Y</pubmed_authors><pubmed_authors>Steinruecke F</pubmed_authors><pubmed_authors>Salo-Mullen E</pubmed_authors><pubmed_authors>Berger M</pubmed_authors><pubmed_authors>Mondaca S</pubmed_authors><pubmed_authors>Connell L</pubmed_authors><pubmed_authors>Saltz LB</pubmed_authors><pubmed_authors>Vakiani E</pubmed_authors><pubmed_authors>Chatila WK</pubmed_authors><pubmed_authors>Shia J</pubmed_authors><pubmed_authors>Krishnan A</pubmed_authors><pubmed_authors>Weiser M</pubmed_authors><pubmed_authors>Palmaira L</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Comprehensive Comparison of Early-Onset and Average-Onset Colorectal Cancers.</name><description>&lt;h4>Background&lt;/h4>The causative factors for the recent increase in early-onset colorectal cancer (EO-CRC) incidence are unknown. We sought to determine if early-onset disease is clinically or genomically distinct from average-onset colorectal cancer (AO-CRC).&lt;h4>Methods&lt;/h4>Clinical, histopathologic, and genomic characteristics of EO-CRC patients (2014-2019), divided into age 35 years and younger and 36-49 years at diagnosis, were compared with AO-CRC (50 years and older). Patients with mismatch repair deficient tumors, CRC-related hereditary syndromes, and inflammatory bowel disease were excluded from all but the germline analysis. All statistical tests were 2-sided.&lt;h4>Results&lt;/h4>In total, 759 patients with EO-CRC (35 years, n = 151; 36-49 years, n = 608) and AO-CRC (n = 687) were incl</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-09T03:11:33.68Z</modification><creation>2025-04-19T23:12:49.623Z</creation></dates><accession>S-EPMC8634406</accession><cross_references><pubmed>34405229</pubmed><doi>10.1093/jnci/djab124</doi></cross_references></HashMap>