Status: Recruiting

Official Title: An open label study to assess the resection rate of liver metastases following neoadjuvant therapy with Avastin in combination with oxaliplatin and capecitabine (XELOX) in patients with metastatic colorectal cancer with unresectable liver metastasis

Brief Summary: This single arm study will assess the resection rate of liver metastasis, time to disease progression, and safety of neoadjuvant treatment with Avastin in combination with oxaliplatin and capecitabine (XELOX) in patients with metastatic colorectal cancer with unresectable liver metastasis. Patients will receive Avastin 5mg/kg iv on day 1 of every 2 week cycle, oxaliplatin 85mg/m2 iv on day 1 of every 2 week cycle, and capecitabine 1000mg/m2 on days 1-5 and 8-12 of every 2 week cycle. The anticipated time on study treatment is 3-12 months, and the target sample size is <100 individuals.

Study Phase: 2

Study Type: Interventional; Prevention; Non-Randomized; Open Label; Uncontrolled; Parallel; Safety/Efficacy study

Condition: Colorectal Cancer

Intervention Type: Drug

Intervention Name: capecitabine [Xeloda]

• adult patients, <=75 years of age;
• chemotherapy-naive for stage IV colorectal cancer with unresectable liver metastasis;
• >=1 measurable lesion;
• ECOG status 0-2.

• prior exposure to Avastin;
• clinical or radiological evidence of CNS metastases;
• uncontrolled hypertension, or clinically significant cardiovascular disease;
• ongoing treatment with aspirin (>325mg/day) or other medications known to predispose to gastrointestinal ulceration.

This trial will be conducted at the following locations:

• TAIPEI 112
• KAOHSIUNG
• CHAI YI
• TAIPEI
• KUEISHAN
• TAICHUNG
• KAOHSIUNG