<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(17)</volume><submitter>Parente P</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Colorectal cancer (CRC) is the third most frequent malignancy and the second cause of cancer-related death worldwide. CRC is characterized by morphologic and biological heterogeneity, and molecular profiling is required to select appropriate treatment in the metastatic setting. Mutations in &lt;i>KRAS&lt;/i> are detected in approximately 40% of CRCs, with prognostic and predictive value, and with the most frequent being p.G12D. Nonetheless, there are few data on the morphologic features in &lt;i&gt;KRAS&lt;/i>-mutated CRCs.&lt;h4>Materials and methods&lt;/h4>We retrospectively collected clinicopathological features and molecular profiles of CRCs in a multicenter cohort.&lt;h4>Results&lt;/h4>A total of 2816 patients from 12 centers were included. &lt;i>KRAS&lt;/i> mutation was found in 47.4% of cases; </pubmed_abstract><journal>Cancers</journal><pagination>2721</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12427293</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&amp;lt;i&amp;gt;KRAS&amp;lt;/i&amp;gt; Mutations in Colorectal Adenocarcinoma: Incidence and Association with Histological Features with Particular Reference to &amp;lt;i&amp;gt;Gly12Asp&amp;lt;/i&amp;gt; in a Multicenter GIPAD Real-World Study.</pubmed_title><pmcid>PMC12427293</pmcid><pubmed_authors>Antoci F</pubmed_authors><pubmed_authors>Ascione A</pubmed_authors><pubmed_authors>Ambrosio MR</pubmed_authors><pubmed_authors>Gafa R</pubmed_authors><pubmed_authors>Pasculli B</pubmed_authors><pubmed_authors>Pilozzi E</pubmed_authors><pubmed_authors>Vasuri F</pubmed_authors><pubmed_authors>Vanoli A</pubmed_authors><pubmed_authors>Parente P</pubmed_authors><pubmed_authors>Giobbe M</pubmed_authors><pubmed_authors>Fassan M</pubmed_authors><pubmed_authors>Grillo F</pubmed_authors><pubmed_authors>Adotti F</pubmed_authors><pubmed_authors>Macciomei MC</pubmed_authors><pubmed_authors>Mastracci L</pubmed_authors><pubmed_authors>Lanza G</pubmed_authors><pubmed_authors>Petrelli F</pubmed_authors><pubmed_authors>Angerilli V</pubmed_authors><pubmed_authors>Gasparello J</pubmed_authors><pubmed_authors>Caputo A</pubmed_authors><pubmed_authors>Gandolfi L</pubmed_authors><pubmed_authors>Melocchi L</pubmed_authors><pubmed_authors>Parrella P</pubmed_authors><pubmed_authors>Scarpino S</pubmed_authors><pubmed_authors>Veccia N</pubmed_authors><pubmed_authors>Saragoni L</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;KRAS&amp;lt;/i&amp;gt; Mutations in Colorectal Adenocarcinoma: Incidence and Association with Histological Features with Particular Reference to &amp;lt;i&amp;gt;Gly12Asp&amp;lt;/i&amp;gt; in a Multicenter GIPAD Real-World Study.</name><description>&lt;h4>Introduction&lt;/h4>Colorectal cancer (CRC) is the third most frequent malignancy and the second cause of cancer-related death worldwide. CRC is characterized by morphologic and biological heterogeneity, and molecular profiling is required to select appropriate treatment in the metastatic setting. Mutations in &lt;i>KRAS&lt;/i> are detected in approximately 40% of CRCs, with prognostic and predictive value, and with the most frequent being p.G12D. Nonetheless, there are few data on the morphologic features in &lt;i&gt;KRAS&lt;/i>-mutated CRCs.&lt;h4>Materials and methods&lt;/h4>We retrospectively collected clinicopathological features and molecular profiles of CRCs in a multicenter cohort.&lt;h4>Results&lt;/h4>A total of 2816 patients from 12 centers were included. &lt;i>KRAS&lt;/i> mutation was found in 47.4% of cases; </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-23T03:19:04.592Z</modification><creation>2026-04-23T03:11:23.844Z</creation></dates><accession>S-EPMC12427293</accession><cross_references><pubmed>40940818</pubmed><doi>10.3390/cancers17172721</doi></cross_references></HashMap>