The BiTE (bispecific T-cell engager) platform: Development and future potential of a targeted immuno-oncology therapy across tumor types
- Cancer. 2020 Jul 15;126(14):3192-3201. doi: 10.1002/cncr.32909.
- 1. Department of Internal Medicine II, Universität Würzburg, Würzburg, Germany.
- 2. Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
- 3. Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas.
- 4. Department of Medicine III, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
- 5. Weill Cornell Medicine, Division of Hematology and Oncology, The New York Presbyterian Hospital, New York, New York.
- 6. Amgen Research (Munich) GmbH, Munich, Germany.
- 7. Amgen Inc., Thousand Oaks, California.
- 8. Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
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.
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