This prospective observational study will evaluate the safety and efficacy of first-line Avastin (bevacizumab) in combination with standard chemotherapy in routine clinical practice in patients with metastatic cancer of the colon and/or rectum. Patients will be followed for the duration of their treatment and a 30-day follow-up after the last dose of study drug.
Study Type
OBSERVATIONAL
Enrollment
35
Unnamed facility
Podgorica, Montenegro
Safety: Incidence of adverse events
Time frame: approximately 3.5 years
Efficacy: Time to disease progression
Time frame: approximately 3.5 years
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