<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/2040763</full_dataset_link><location>Canada</location><study_start_month>12</study_start_month><keyword>Xeloda</keyword><keyword>Irinotecan</keyword><keyword>Colorectal</keyword><keyword>CPT-11</keyword><keyword>Rectal</keyword><keyword>Capecitabine</keyword><keyword>Camptothecin-11</keyword><keyword>Metastatic</keyword><keyword>Colon</keyword><keyword>Avastin</keyword><keyword>Bevacizumab</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>A Phase II Study of Bevacizumab, Irinotecan and Capecitabine in Patients With Previously Untreated Metastatic Colorectal Cancer</name><description>Bevacizumab has recently been shown to improve survival when combined with chemotherapy in patients with previously untreated metastatic colorectal cancer. Bevacizumab is usually given together with infusional 5-FU, which requires a central line. A central line is inconvenient for patients, and may increase risk of infection, and thrombosis. Furthermore, a central line increases resource demands for interventional radiology, chemo daycare. Capecitabine is administered orally, and converted to 5-FU intracellularly. Chronic administration of capecitabine mimics infusional 5-FU. This study is designed to evaluate whether the combination of irinotecan, capecitabine and bevacizumab is effective as a first-line therapy for patients with metastatic colorectal cancer.</description><dates><creation>2006-12-15</creation></dates><accession>2040763</accession><cross_references><ClinicalTrials___gov>NCT00483834</ClinicalTrials___gov></cross_references></HashMap>