This 2 arm study will assess the efficacy and safety of Avastin in combination with irinotecan + 5-fluorouracil/folinic acid, versus irinotecan + fluorouracil/folinic acid alone, as first line treatment in Chinese patients with metastatic colorectal cancer. Patients will be randomized 2:1 to receive 6-weekly cycles of Avastin (5mg/kg iv every 2 weeks) + irinotecan 125mg/m2 iv / leucovorin 20mg/m2 iv / fluorouracil 500mg/m2 iv weekly for 4 weeks, or 6-weekly cycles of irinotecan 125mg/m2 iv / leucovorin 20mg/m2 iv / fluorouracil 500mg/m2 iv weekly for 4 weeks. The anticipated time on study treatment is until disease progression, and the sample size is 100-500 individuals.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
214
5mg/kg iv every 2 weeks
125mg/m2 iv weekly for 4 weeks of each 6 week cycle
20mg/m2 iv weekly for 4 weeks of each 6 week cycle
500mg/m2 iv weekly for 4 weeks of each 6 week cycle
Unnamed facility
Beijing, China
Unnamed facility
Beijing, China
Unnamed facility
Beijing, China
Unnamed facility
Chongqing, China
Unnamed facility
Guangdong, China
Unnamed facility
Guangzhou, China
Unnamed facility
Nanjing, China
Unnamed facility
Qingdao, China
Unnamed facility
Shanghai, China
Unnamed facility
Shanghai, China
...and 2 more locations
Progression-free survival.
Time frame: 6 months
Overall response rate, time to response, duration of response, overall survival.
Time frame: Event driven
AEs, laboratory tests
Time frame: Throughout study
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