| Literature DB >> 33130314 |
Norihiro Watanabe1, Mary Kathryn McKenna1, Amanda Rosewell Shaw1, Masataka Suzuki2.
Abstract
Immunotherapy has recently garnered success with the induction of clinical responses in tumors, which are traditionally associated with poor outcomes. Chimeric antigen receptor T (CAR-T) cells and oncolytic viruses (OVs) have emerged as promising cancer immunotherapy agents. Herein, we provide an overview of the current clinical status of CAR-T cell and OV therapies. While preclinical studies have demonstrated curative potential, the benefit of CAR-T cells and OVs as single-agent treatments remains limited to a subset of patients. Combinations of different targeted therapies may be required to achieve efficient, durable responses against heterogeneous tumors, as well as the microenvironment. Using a combinatorial approach to take advantage of the unique features of CAR-T cells and OVs with other treatments can produce additive therapeutic effects. This review also discusses ongoing clinical evaluations of these combination strategies for improved outcomes in treatment of resistant malignancies.Entities:
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Year: 2020 PMID: 33130314 PMCID: PMC7854303 DOI: 10.1016/j.ymthe.2020.10.023
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454