Advance or recurrent colorectal cancer.
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Patient With estimative lesion and Histological confirmation of colorectal cancer. (2) Patients with unresectable colorectal cancer who had received no previous therapy. (3) Patient who is scheduled to be administered the combination of XELOX + Bevacizumab. (4) Patient who is 20 years old or more. (5) Eastern Cooperative Oncology Group (ECOG) performance status (PS) : 0 - 2. (6) Appropriate for the study at the physician's assessment. (7) Written informed consent.
Exclusion criteria
Exclusion criteria: (1)Patient who fall under the a package insert "contraindication" or "Contraindicaton in combination" with Bevacizumab , Oxaliplatin and Capecitabine. (2) Not appropriate for the study at the physician's assessment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression free survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Response rate Response rate at the fourth course Time-to-treatment failure Overall survival Resection rate in subjects with liver metastasis R0 resection rate in subjects with liver metastasis Safety Assessment of Quality of life (Dermatology Life Quality Index) | — |
Countries
Japan
Contacts
Tokyo Medical University The third department of surgery