<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>126(5)</volume><submitter>Larsen SG</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Patients with metastatic colorectal cancer (mCRC) carrying BRAF (mutBRAF) or KRAS mutation (mutKRAS) have an inferior prognosis after liver or lung surgery, whereas the prognostic role in the context of peritoneal metastasis (PM) after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has been less investigated.&lt;h4>Methods&lt;/h4>In total, 257 patients with non-appendiceal PM-CRC were included from the Norwegian National Unit for CRS-HIPEC.&lt;h4>Results&lt;/h4>In total, 180 patients received CRS-HIPEC with Mitomycin C, 77 patients received palliative surgery only. In the CRS-HIPEC group, mutBRAF was found in 24.7%, mutKRAS 33.9% and double wild-type 41.4% without differences in survival. MSI was found in 29.3% of mutBRAF cases. Patients with mutBR</pubmed_abstract><journal>British journal of cancer</journal><pagination>726-735</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8888568</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of KRAS, BRAF and microsatellite instability status after cytoreductive surgery and HIPEC in a national cohort of colorectal peritoneal metastasis patients.</pubmed_title><pmcid>PMC8888568</pmcid><pubmed_authors>Dueland S</pubmed_authors><pubmed_authors>Flatmark K</pubmed_authors><pubmed_authors>Dagenborg VJ</pubmed_authors><pubmed_authors>Torgunrud A</pubmed_authors><pubmed_authors>Hofsli E</pubmed_authors><pubmed_authors>Sorbye H</pubmed_authors><pubmed_authors>Steigen SE</pubmed_authors><pubmed_authors>Lund-Iversen M</pubmed_authors><pubmed_authors>Larsen SG</pubmed_authors><pubmed_authors>Goscinski MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of KRAS, BRAF and microsatellite instability status after cytoreductive surgery and HIPEC in a national cohort of colorectal peritoneal metastasis patients.</name><description>&lt;h4>Background&lt;/h4>Patients with metastatic colorectal cancer (mCRC) carrying BRAF (mutBRAF) or KRAS mutation (mutKRAS) have an inferior prognosis after liver or lung surgery, whereas the prognostic role in the context of peritoneal metastasis (PM) after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has been less investigated.&lt;h4>Methods&lt;/h4>In total, 257 patients with non-appendiceal PM-CRC were included from the Norwegian National Unit for CRS-HIPEC.&lt;h4>Results&lt;/h4>In total, 180 patients received CRS-HIPEC with Mitomycin C, 77 patients received palliative surgery only. In the CRS-HIPEC group, mutBRAF was found in 24.7%, mutKRAS 33.9% and double wild-type 41.4% without differences in survival. MSI was found in 29.3% of mutBRAF cases. Patients with mutBR</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T13:21:49.868Z</modification><creation>2025-04-04T13:21:49.868Z</creation></dates><accession>S-EPMC8888568</accession><cross_references><pubmed>34887523</pubmed><doi>10.1038/s41416-021-01620-6</doi></cross_references></HashMap>