Induced Vascular Normalization-Can One Force Tumors to Surrender to a Better Microenvironment?

Pharmaceutics. 2023 Jul 26;15(8):2022. doi: 10.3390/pharmaceutics15082022.

Abstract

Immunotherapy has changed the way many cancers are being treated. Researchers in the field of immunotherapy and tumor immunology are investigating similar questions: How can the positive benefits achieved with immunotherapies be enhanced? Can this be achieved through combinations with other agents and if so, which ones? In our view, there is an urgent need to improve immunotherapy to make further gains in the overall survival for those patients that should benefit from immunotherapy. While numerous different approaches are being considered, our team believes that drug delivery methods along with appropriately selected small-molecule drugs and drug candidates could help reach the goal of doubling the overall survival rate that is seen in some patients that are given immunotherapeutics. This review article is prepared to address how immunotherapies should be combined with a second treatment using an approach that could realize therapeutic gains 10 years from now. For context, an overview of immunotherapy and cancer angiogenesis is provided. The major targets in angiogenesis that have modulatory effects on the tumor microenvironment and immune cells are highlighted. A combination approach that, for us, has the greatest potential for success involves treatments that will normalize the tumor's blood vessel structure and alter the immune microenvironment to support the action of immunotherapeutics. So, this is reviewed as well. Our focus is to provide an insight into some strategies that will engender vascular normalization that may be better than previously described approaches. The potential for drug delivery systems to promote tumor blood vessel normalization is considered.

Keywords: anti-angiogenesis; cancer angiogenesis; drug repurposing; immune cells; immune checkpoint inhibitors; immunotherapy; nanomedicine; tumor vascular normalization.

Publication types

  • Review

Grants and funding

Marcel B. Bally received funding from the following sources: Canadian Institutes of Health Research (CIHR) grant number: PJT-178415 and the Nanomedicine Innovation Network DRG 03190. Kevin L. Bennewith receives funding from CIHR grant number: PJT 178406. Che-Min Lee receives Four Year Fellowship funding from the University of British Columbia.