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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
  1. 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
  2. Patients who will receive irinotecan, a component of FOLFIRI regimen, using Camtop Injection®
Exclusion Criteria
  1. 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
NameTimeMethod
percentage of use FOLFIRI regimen and target agentsthrough study completion, 3 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Yonsei University Health System, Severance Hospital

🇰🇷

Seoul, Korea, Republic of

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