| Literature DB >> 32401342 |
Hermann Einsele1, Hossein Borghaei2, Robert Z Orlowski3, Marion Subklewe4, Gail J Roboz5, Gerhard Zugmaier6, Peter Kufer6, Karim Iskander7, Hagop M Kantarjian8.
Abstract
Immuno-oncology therapies engage the immune system to treat cancer. BiTE (bispecific T-cell engager) technology is a targeted immuno-oncology platform that connects patients' own T cells to malignant cells. The modular nature of BiTE technology facilitates the generation of molecules against tumor-specific antigens, allowing off-the-shelf immuno-oncotherapy. Blinatumomab was the first approved canonical BiTE molecule and targets CD19 surface antigens on B cells, making blinatumomab largely independent of genetic alterations or intracellular escape mechanisms. Additional BiTE molecules in development target other hematologic malignancies (eg, multiple myeloma, acute myeloid leukemia, and B-cell non-Hodgkin lymphoma) and solid tumors (eg, prostate cancer, glioblastoma, gastric cancer, and small-cell lung cancer). BiTE molecules with an extended half-life relative to the canonical BiTE molecules are also being developed. Advances in immuno-oncology made with BiTE technology could substantially improve the treatment of hematologic and solid tumors and offer enhanced activity in combination with other treatments.Entities:
Keywords: B cell; T cell; blinatumomab; hematologic malignancies; tumor-specific antigen
Mesh:
Substances:
Year: 2020 PMID: 32401342 DOI: 10.1002/cncr.32909
Source DB: PubMed Journal: Cancer ISSN: 0008-543X Impact factor: 6.860