<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2013</study_start_year><data_sharing_plan>IPD Sharing (as of March 2018): Undecided</data_sharing_plan><condition>Metastatic Colorectal Cancer</condition><condition>Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><condition>Metastatic colorectal cancer</condition><condition>Metastases</condition><disease>Metastatic Colorectal Cancer</disease><disease>Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><disease>Metastases</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2149795</full_dataset_link><location>Netherlands</location><study_start_month>12</study_start_month><keyword>Capecitabine</keyword><keyword>Hand-foot syndrome</keyword><keyword>S1</keyword><keyword>Teysuno</keyword><keyword>Fluoropyrimidine</keyword><keyword>Bevacizumab</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>S-1 Versus Capecitabine in the First Line Treatment of MCC Patients.</name><description>The study is a two-arm randomised phase III trial. Patients will be randomised to receive capecitabine (arm A) or S-1 (arm B). Bevacizumab may be added according to the choice of the investigator. Patients will be followed 3-weekly at the outpatient clinic, toxicity will be assessed according to study protocol guidelines. Patients will be evaluated every 3 cycles for response. Upon disease progression patients will be treated according to the local investigators</description><dates><creation>2013-12-15</creation></dates><accession>2149795</accession><cross_references><ClinicalTrials___gov>NCT01918852</ClinicalTrials___gov><EU Clinical Trials Register>2013-002147-28</EU Clinical Trials Register></cross_references></HashMap>