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This combination therapy regimen, being evaluated by Yonsei University, consists of the angiogenesis inhibitor bevacizumab (Avastin) and a modified FOLFIRINOX chemotherapy backbone (oxaliplatin, irinotecan, leucovorin, and 5-fluorouracil). It is specifically designed to treat rare mucinous gynecologic cancers, including mucinous ovarian, fallopian tube, and primary peritoneal carcinomas, which typically exhibit poor responses to standard platinum-based treatments. Bevacizumab is a recombinant humanized monoclonal antibody that targets vascular endothelial growth factor-A (VEGF-A), while the FOLFIRINOX components provide multi-targeted cytotoxic activity similar to regimens used in gastrointestinal malignancies.
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