Table 3.
Paradigm | Example | Approved * | Target |
---|---|---|---|
mAbs that target tumors | Herceptin | Yes | Herceptin is approved for the treatment of early-stage breast cancer that is human epidermal growth factor receptor 2-positive (HER2+). |
Transfer of adoptive cells | Vemurafenib | No | Vemurafenib is used to slow the growth of certain types of cancer cells. |
Oncolytic viruses | RIGVIR, Oncorine, and T-VEC | Yes | The treatment, which is injected into tumors, was engineered to produce a protein that stimulates the production of immune cells in the body and to reduce the risk of causing herpes. |
DC-based therapies | _ | No | Targeted treatment that involves extracting and manipulating components of a patient’s immune system (the dendritic cells) to boost its chances of eliminating unnoticed cancer cells. |
Vaccinations based on peptides | TAS0314 | Yes | Dramatically suppressed tumor growth. |
Immunomodulatory mAbs | Rituximab (Rituxan) | Yes | It specifically targets the CD20 protein. B-cells, a type of white blood cell, have CD20, and it is indicated in patients for non-Hodgkin’s lymphoma and chronic lymphocytic leukemia. |
Immunostimulatory cytokines | IFN-α | Yes | Approved for the treatment of some hematological malignancies and AIDS-related Kaposi sarcoma. |
Immunosuppressive metabolism inhibitors | Rapamycin | No | Decrease the risk of organ transplant patients to develop cancer. |
PRR agonists | Imiquimod | Yes | To achieve the purpose of regulating immunity and treating tumors. |
ICD inducers | Radiation | Yes | The best-characterized inducer of immunogenic cell death. |
* In one of its forms for use in cancer patients, by the US Food and Drug Administration or an equivalent regulatory agency worldwide.