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| Funder | NATIONAL CANCER INSTITUTE |
|---|---|
| Recipient Organization | University of Southern California |
| Country | United States |
| Start Date | Aug 01, 2024 |
| End Date | Jul 31, 2026 |
| Duration | 729 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10879652 |
PROJECT SUMMARY: Disparities in cancer outcomes in certain patient populations such as Hispanic/Latino (H/L) patients, are rooted in part in the lack of understanding of biologic factors and mechanisms of response or resistance to novel therapeutics. Although most patients express a willingness to participate in clinical research, only approximately
8% of adult cancer patients enroll in cancer clinical trials, and the percentage of minorities participating in clinical trials, overall, is much lower when compared to the general population of the U.S. H/L’s, and other minority groups, for example, continue to be under-represented in clinical trials. The under-representation of minority
groups in cancer research contributes to disparities in cancer care and outcomes by failing to provide the evidence that clinicians and scientists need to safely treat and discover new treatments for minority patients with cancer. This project enables an integrative analysis of demographic, and clinical data combined with multi-omics
approaches using blood samples and tissue from breast cancer patients to elucidate the differences in immune response to breast cancer in patients of H/L race. Immune checkpoint inhibition (ICI) is a type of immunotherapy that has revolutionized treatment for many patients with breast cancer. However, complex immunosuppressive
tumor microenvironments (TMEs) within breast cancers render them less responsive to ICIs and present therapeutic obstacles. Specifically, recruitment of myeloid-derived suppressor cells (MDSCs) prohibit T-cell activation and infiltration which leads to successful treatment with this class of therapeutics. We aim to
characterize differences in the suppressive TME by race and tumor subtype. Understanding these differences will affect development of novel treatment combinations & strategies. The identification of patient populations with higher risk disease, most likely to benefit from ICIs is of equal importance to understanding of scientific
mechanisms. H/L patients have a higher percentage of young women (
University of Southern California
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