Treatment with Anti-vegf antibodies
a technology of anti-vegf antibodies and anti-cancer drugs, applied in the direction of cardiovascular disorders, drug compositions, peptides, etc., can solve the problems of numerous side effects, difficult detection and treatment, and current cancer treatment methods that are relatively non-selectiv
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Addition of an Anti-VEGF Antibody to Bolus Irinotecan / Fluorouracil / Leucovorin (IFL) in First Line Metastatic Colorectal Cancer
[0193] A multicenter, Phase III, randomized, active-controlled trial was conducted to evaluate the efficacy and safety of bevacizumab when added to standard first-line chemotherapy used to treat metastatic colorectal cancer. The trial enrolled over 900 patients with histologically confirmed, previously untreated, bi-dimensionally measurable metastatic colorectal cancer.
Methods and Materials
Anti-VEGF Antibody bevacizumab
[0194] The anti-VEGF antibody “Bevacizumab (BV)”, also known as “rhuMAb VEGF”or “Avastin™”, is a recombinant humanized anti-VEGF monoclonal antibody generated according to Presta et al. (1997) Cancer Res. 57:4593-4599. It comprises mutated human IgG1 framework regions and antigen-binding complementarity-determining regions from the murine anti-hVEGF monoclonal antibody A.4.6.1 that blocks binding of human VEGF to its receptors. U.S. Pat. ...
example 2
Addition of Bevacizumab to Bolus 5-FU / Leucovorin in First-Line Metastatic Colorectal Cancer
[0227] This randomized, phase II trial compared bevacizumab plus 5-fluorouracil and leucovorin (5-FU / LV) versus placebo plus 5-FU / LV as first-line therapy in patients considered non-optimal candidates for first-line irinotecan.
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Patient Eligibility
[0228] Patients with histologically confirmed, previously untreated, measurable metastatic colorectal cancer were eligible if, in the judgment of the investigator, they were not optimal candidates for first-line irinotecan-containing therapy and had at least one of the following characteristics: age above 65 years, ECOG PS of 1 or 2, serum albumin equal or less than 3.5 g / dL, or prior radiotherapy to abdomen or pelvis. Patients were excluded if they had undergone major surgical procedures or open biopsy, or had experienced significant traumatic injury, within 28 days prior to study entry; anticipated need for major surgery dur...
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