<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang DS</submitter><funding>Guangdong Basic and Applied Basic Research Foundation</funding><funding>National Natural Science Foundation of China</funding><pagination>e1004389</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11086847</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>It remains unclear whether intensification of the chemotherapy backbone in tandem with an anti-EGFR can confer superior clinical outcomes in a cohort of RAS/BRAF wild-type colorectal cancer (CRC) patients with initially unresectable colorectal liver metastases (CRLM). To that end, we sought to comparatively evaluate the efficacy and safety of cetuximab plus FOLFOXIRI (triplet arm) versus cetuximab plus FOLFOX (doublet arm) as a conversion regimen (i.e., unresectable to resectable) in CRC patients with unresectable CRLM.&lt;h4>Methods and findings&lt;/h4>This open-label, randomized clinical trial was conducted from April 2018 to December 2022 in 7 medical centers across China, enrolling 146 RAS/BRAF wild-type CRC patients with initially unresectable CRLM. A stratified blocked r</pubmed_abstract><journal>PLoS medicine</journal><pubmed_title>Cetuximab plus FOLFOXIRI versus cetuximab plus FOLFOX as conversion regimen in RAS/BRAF wild-type patients with initially unresectable colorectal liver metastases (TRICE trial): A randomized controlled trial.</pubmed_title><pmcid>PMC11086847</pmcid><funding_grant_id>82073302</funding_grant_id><funding_grant_id>2023B1515020015</funding_grant_id><pubmed_authors>Chen JQ</pubmed_authors><pubmed_authors>Qiu MZ</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Liu TS</pubmed_authors><pubmed_authors>Fong WP</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Pan ZZ</pubmed_authors><pubmed_authors>Xie DJ</pubmed_authors><pubmed_authors>Wan DS</pubmed_authors><pubmed_authors>Xu RH</pubmed_authors><pubmed_authors>Wang ZQ</pubmed_authors><pubmed_authors>Ding PR</pubmed_authors><pubmed_authors>Li SS</pubmed_authors><pubmed_authors>Wang FH</pubmed_authors><pubmed_authors>Wang XZ</pubmed_authors><pubmed_authors>Luo HY</pubmed_authors><pubmed_authors>Chen T</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors><pubmed_authors>Yuan YF</pubmed_authors><pubmed_authors>Lu ZH</pubmed_authors><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Wu XJ</pubmed_authors><pubmed_authors>Wang LY</pubmed_authors><pubmed_authors>Wang DS</pubmed_authors><pubmed_authors>Ren C</pubmed_authors><pubmed_authors>Li YH</pubmed_authors><pubmed_authors>Li BK</pubmed_authors><pubmed_authors>Zhai XH</pubmed_authors><pubmed_authors>Xiao J</pubmed_authors><pubmed_authors>Li LR</pubmed_authors><pubmed_authors>Tan Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cetuximab plus FOLFOXIRI versus cetuximab plus FOLFOX as conversion regimen in RAS/BRAF wild-type patients with initially unresectable colorectal liver metastases (TRICE trial): A randomized controlled trial.</name><description>&lt;h4>Background&lt;/h4>It remains unclear whether intensification of the chemotherapy backbone in tandem with an anti-EGFR can confer superior clinical outcomes in a cohort of RAS/BRAF wild-type colorectal cancer (CRC) patients with initially unresectable colorectal liver metastases (CRLM). To that end, we sought to comparatively evaluate the efficacy and safety of cetuximab plus FOLFOXIRI (triplet arm) versus cetuximab plus FOLFOX (doublet arm) as a conversion regimen (i.e., unresectable to resectable) in CRC patients with unresectable CRLM.&lt;h4>Methods and findings&lt;/h4>This open-label, randomized clinical trial was conducted from April 2018 to December 2022 in 7 medical centers across China, enrolling 146 RAS/BRAF wild-type CRC patients with initially unresectable CRLM. A stratified blocked r</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-03T01:32:17.073Z</modification><creation>2026-04-22T03:13:20.079Z</creation></dates><accession>S-EPMC11086847</accession><cross_references><pubmed>38728364</pubmed><doi>10.1371/journal.pmed.1004389</doi></cross_references></HashMap>