<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2006</study_start_year><condition>Colorectal cancer</condition><condition>Colorectal Neoplasms</condition><disease>Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2044346</full_dataset_link><location>South Korea</location><study_start_month>8</study_start_month><keyword>Oxaliplatin</keyword><keyword>Phase I/II study</keyword><keyword>TS-1 and oxaliplatin</keyword><keyword>First line treatment</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>A Phase I/II Trial of TS-1 and Oxaliplatin in Patients With Advanced Colorectal Cancer</name><description>Capecitabine and oxaliplatin(XELOX) is active first-line therapy for patients with metastatic colorectal cancer. Phase II study of TS-1, a novel oral fluoropyrimidine derivative, showed activity in patients with metastatic colorectal carcinoma. Preclinical data of TS-1 with oxaliplatin showed synergistic activity in vivo human colorectal cancer xenograft. There is no data about the optimal dose of TS-1 with 2 weeks schedule combined with oxaliplatin. Therefore in a phase I study, we would like to determine the maximum tolerated dose(MTD) of TS-1 and oxaliplatin and define the recommended dose for subsequent phase II study. And then, in a phase II study we would like to evaluate the efficacy(response rates) and toxicities of the new combination regimen in advanced colorectal cancer.</description><dates><creation>2006-08-15</creation></dates><accession>2044346</accession><cross_references><ClinicalTrials___gov>NCT00531245</ClinicalTrials___gov></cross_references></HashMap>