Observe adverse events and efficacy in recruited patients for 3 years under real world settings.
Enrollment
1,800 estimated patients
Sex
All
Ages
19+ years old
Volunteers
No Healthy Volunteers
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.