Copyright
©The Author(s) 2019.
World J Clin Oncol. Feb 24, 2019; 10(2): 52-61
Published online Feb 24, 2019. doi: 10.5306/wjco.v10.i2.52
Published online Feb 24, 2019. doi: 10.5306/wjco.v10.i2.52
Agent | Class | Target | Indication | Approved for | Recommended dose |
Bevacizumab | Humanized Moab | VEGF-A | First- and second-line | Use in combination with oxaliplatin and irinotecan-based chemotherapy | 5 mg/kg or 10 mg/kg i.v. every 2 wk |
Aflibercept | Fully human Moab | VEGF-A, -B, and PIGF | Second-line | Use in combination with FOLFIRI | 4 mg/kg i.v. every 2 wk |
Ramucirumab | Fully human Moab | The extracellular domain of VEGFR-2 | Second-line | Use in combination with FOLFIRI | 8 mg/kg i.v. every 2 wk |
Regorafenib | Oral multikinase inhibitor | VEGFR-1, -2, and -3 (in addition to RET, KIT, PDGFR, and FGFR | Beyond second-line | Single-use | 160 mg once daily, days 1-21 of 28-d cycle |
- Citation: Kanat O, Ertas H. Existing anti-angiogenic therapeutic strategies for patients with metastatic colorectal cancer progressing following first-line bevacizumab-based therapy. World J Clin Oncol 2019; 10(2): 52-61
- URL: https://www.wjgnet.com/2218-4333/full/v10/i2/52.htm
- DOI: https://dx.doi.org/10.5306/wjco.v10.i2.52