The future of cancer immunotherapy: microenvironment-targeting combinations
By Y. Murciano-Goroff, A. B. Warner, J. Wolchok. Cell Research, 2020
621 citations recorded by the source corpus.
Immunotherapy holds the potential to induce durable responses, but only a minority of patients currently respond. The etiologies of primary and secondary resistance to immunotherapy are multifaceted, deriving not only from tumor intrinsic factors, but also from the complex interplay between cancer and its microenvironment. In addressing frontiers in clinical immunotherapy, we describe two categories of approaches to the design of novel drugs and combination therapies: the first involves direct modification of the tumor, while the second indirectly enhances immunogenicity through alteration of the microenvironment. By systematically addressing the factors that mediate resistance, we are able to identify mechanistically-driven novel approaches to improve immunotherapy outcomes.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/e45faa7ac36c53200bb9b7cdcc0b41302c029c64
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Citations in the corpus
- Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics (2022, background): “Upon reinfusion, lymphocytes grown ex vivo may respond more potently to tumor antigen since they have not been continuously exposed to tolerogenic microenvironmental signals.(256) Tumor infiltrating lymphocytes (TIL) treatment,(257) chimeric antigen receptor (CAR) engineered T-cells,(258,259) and TC”