Pattern of Use of Bevacizumab or Cetuximab + FOLFIRI Regimen as First-line Treatment in Metastatic Colorectal Cancer
- Conditions
- Metastatic Colorectal Cancer
- Registration Number
- NCT03286738
- Lead Sponsor
- Joong Bae Ahn
- Brief Summary
* Registry
* Multicenter, prospective observational study
* Observe adverse events and efficacy in recruited patients for 3 years under real world settings.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 1800
Inclusion Criteria
- Adult patients at least 19 years of age with metastatic colorectal cancer who are planned to receive Bevacizumab or Cetuximab in combination with FOLFIRI regimen as first-line treatment
- Patients who will receive irinotecan, a component of FOLFIRI regimen, using Camtop Injection®
Exclusion Criteria
- Patients with conditions in which any study drug is contraindicated per the respective approved label.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method percentage of use FOLFIRI regimen and target agents through study completion, 3 years
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Yonsei University Health System, Severance Hospital
🇰🇷Seoul, Korea, Republic of