<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(2)</volume><submitter>Liu X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The TACTIC CRC-02 study evaluated the efficacy and safety of tislelizumab, a humanized immunoglobulin G4 monoclonal antibody targeting programmed cell death protein 1, combined with standard XELOX plus bevacizumab as first-line treatment of microsatellite stable/proficient mismatch repair (MSS/pMMR) RAS-mutant metastatic colorectal cancer (mCRC).&lt;h4>Patients and methods&lt;/h4>TACTIC CRC-02 was a single-center, single-arm, open-label, phase II trial. Eligible patients had previously untreated, unresectable MSS/pMMR, RAS-mutant mCRC and an Eastern Cooperative Oncology Group performance status of 0 or 1. Patients received intravenous tislelizumab (200 mg/m&lt;sup>2&lt;/sup>), bevacizumab (7.5 mg/kg), and oxaliplatin (130 mg/m&lt;sup>2&lt;/sup>) on day 1, with oral capecitabine (1000 mg/m</pubmed_abstract><journal>ESMO open</journal><pagination>106056</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12870864</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tislelizumab plus bevacizumab and XELOX as first-line treatment of MSS/pMMR RAS-mutant metastatic colorectal cancer (TACTIC CRC-02): a phase II study.</pubmed_title><pmcid>PMC12870864</pmcid><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Cao B</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Ou K</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhou A</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Gao L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tislelizumab plus bevacizumab and XELOX as first-line treatment of MSS/pMMR RAS-mutant metastatic colorectal cancer (TACTIC CRC-02): a phase II study.</name><description>&lt;h4>Background&lt;/h4>The TACTIC CRC-02 study evaluated the efficacy and safety of tislelizumab, a humanized immunoglobulin G4 monoclonal antibody targeting programmed cell death protein 1, combined with standard XELOX plus bevacizumab as first-line treatment of microsatellite stable/proficient mismatch repair (MSS/pMMR) RAS-mutant metastatic colorectal cancer (mCRC).&lt;h4>Patients and methods&lt;/h4>TACTIC CRC-02 was a single-center, single-arm, open-label, phase II trial. Eligible patients had previously untreated, unresectable MSS/pMMR, RAS-mutant mCRC and an Eastern Cooperative Oncology Group performance status of 0 or 1. Patients received intravenous tislelizumab (200 mg/m&lt;sup>2&lt;/sup>), bevacizumab (7.5 mg/kg), and oxaliplatin (130 mg/m&lt;sup>2&lt;/sup>) on day 1, with oral capecitabine (1000 mg/m</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-15T06:15:35.965Z</modification><creation>2026-06-30T03:22:07.091Z</creation></dates><accession>S-EPMC12870864</accession><cross_references><pubmed>41610691</pubmed><doi>10.1016/j.esmoop.2025.106056</doi></cross_references></HashMap>