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- W2981292922 abstract "Introduction: In colorectal cancer, anti-VEGF agents have demonstrated a survival benefit when combined with chemotherapy. However, development of resistance is very common. One of the mechanisms is due not to a failure in the VEGFR blockade, but rather to development of compensatory mechanisms of resistance, such as hypoxia-triggered upregulation of other proangiogenic factors, like placental growth factor (PlGF).Areas covered: This article summarizes the fundamental role of PlGF in the development of resistance to antiangiogenic treatment as well as the efficacy of aflibercept, ramucirumab, and regorafenib.Expert opinion: Aflibercept functions as a soluble decoy receptor precluding VEGFs and PlGF from binding to native VEGFR, and therefore preventing the emergence of resistance. Bevacizumab limits its function to preventing the interaction between VEGF-A and VEGFR. In combination with FOLFIRI (VELOUR trial), aflibercept improves survival in patients with metastatic CRC who are resistant or have progressed to oxaliplatin-based chemotherapy. Ramucirumab, a fully humanized immunoglobulin G1 (IgG-1) monoclonal antibody and regorafenib, a multikinase inhibitor, have significant improvement for overall survival as well as for progression-free survival in chemotherapy refractory settings." @default.
- W2981292922 created "2019-10-25" @default.
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- W2981292922 date "2019-10-16" @default.
- W2981292922 modified "2023-10-07" @default.
- W2981292922 title "The role of PIGF blockade in the treatment of colorectal cancer: overcoming the pitfalls" @default.
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- W2981292922 doi "https://doi.org/10.1080/14712598.2020.1677603" @default.
- W2981292922 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31608707" @default.
- W2981292922 hasPublicationYear "2019" @default.
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