Table 3.
Drug | Target antigen | Ab Type | Phase | Cancer type | Sponsor | |
---|---|---|---|---|---|---|
1 | Bevacizumab (with or w/o Vorinostat, Temozolomide, radiation) | VEGF-A | humanized monoclonal Ab | Ph II, Ph III | High-Grade Glioma | National Cancer Institute (NCI), USA |
2 | Bevacizumab (with or w/o Lomustine) | VEGF-A | humanized monoclonal Ab | Ph III | Recurrent glioblastoma | European Organisation for Research and Treatment of Cancer—EORTC |
3 | Bevacizumab (combined with or w/o Temozolomide and radiation) | VEGF-A | Humanized monoclonal Ab | Ph III | Glioblastoma | National Cancer Institute (NCI), USA |
4 | Nivolumab (with or w/o Bevacizumab and Ipilimumab) |
|
|
Ph III | Recurrent Glioblastoma | Bristol-Myers Squibb |
5 | Nivolumab (with or w/o Temozolomide, Radiation) | PD-1 | Human monoclonal Ab | Ph III | Glioblastoma | Bristol-Myers Squibb |
Currently, the most commonly targeted antigen in glioma by Ab-based drugs is VEGF-A, followed by programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4). All biological treatments include chemo- and/or radio-therapy or the use of other biologicals.