The addition of bevacizumab to these chemotherapy regimens resulted in response rates and Selleck Cediranib Median overall survival durations of 52% and 26.1 months, 39% and 20.4 months, and 46% and 24.6 months, respectively. Based
on the results of the TREE-2 study, the addition of bevacizumab to chemotherapy regimens combining oxaliplatin with fluoropyrimidines is well tolerated and clinically beneficial in the first line management of metastatic colorectal cancer. Table 2 Median overall survival and progression free survival of adding bevacizumab to oxaliplatin-containing chemotherapeutic regimens in the management of first line metastatic colorectal cancer In addition to the TREE-2 study, the N016966 Inhibitors,research,lifescience,medical study also evaluated Inhibitors,research,lifescience,medical the addition of bevacizumab to first-line, oxaliplatin-based chemotherapy. In this study, however, the addition of bevacizumab to chemotherapy was planned from the onset, in order to evaluate the benefit of its inclusion (13). Patients were randomly assigned in a 2×2 analysis to receive a chemotherapeutic regimen of either XELOX or FOLFOX4 (which uses both bolus and infusion 5-fluorouracil). The patients were then randomized Inhibitors,research,lifescience,medical to receive either bevacizumab (at either 7.5 or 5 mg/kg depending
on cycle length) or placebo. A statistically significant improvement in the primary endpoint of progression free survival was noted when bevacizumab was added to one of these oxaliplatin-containing Inhibitors,research,lifescience,medical regimens (13). However, no statistically significant difference in overall survival resulted with the addition of bevacizumab, and the response rates were similar with or without the use of bevacizumab. These survival data
are summarized in Table 2. The lack of overall survival benefit may be attributed to cessation of treatment prior to disease progression in many patients in this study; had it been continued to disease progression, a benefit may have been observed, as has been demonstrated in some analyses. Taking this criticism into account, and considering that the rates of adverse events related to the use of Inhibitors,research,lifescience,medical bevacizumab remained manageable, the use of bevacizumab in addition to an oxaliplatin-based first line chemotherapy regimen remains appropriate practice for the management ADAMTS5 for metastatic colorectal cancer. The results of a phase II trial in patients aged 65 and above demonstrated that the addition of bevacizumab to 5-fluorouracil alone, without either irinotecan or oxaliplatin, was of added clinical benefit over 5-fluorouracil alone, in the first-line management of metastatic colorectal cancer (14). In this trial, all patients were assigned to receive chemotherapy consisting of leucovorin and bolus 5-fluorouracil, and were randomized to receive either bevacizumab (at 5 mg/kg with each cycle) or placebo. This study did not achieve a statistically significant improvement in median overall survival through the addition of bevacizumab to 5-fluorouracil.