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Active NON-SBIR/STTR RPGS NIH (US)

Elucidating resistance mechanisms and enhancing response to immune checkpoint blockade in central nervous system metastases from breast cancer

$7.01M USD

Funder NATIONAL CANCER INSTITUTE
Recipient Organization Massachusetts General Hospital
Country United States
Start Date Jul 12, 2024
End Date Jun 30, 2029
Duration 1,814 days
Number of Grantees 2
Roles Principal Investigator; Co-Investigator
Data Source NIH (US)
Grant ID 10997794
Grant Description

PROJECT SUMMARY Metastases to the central nervous system (CNS) are a common complication of breast cancer. Prognosis is typically on the order of a few months. Immunotherapies have revolutionized the management of many types of cancers. However, these agents have not been systematically studied in the management of CNS metastases

from breast cancer. We are conducting several Phase II trials to explore the role of newly developed immunotherapies in CNS metastases. Three of our trials have already met primary endpoint, with a subset of patients with breast cancer showing responses to immunotherapy. We propose to study cancer genetic and

immune phenotypic changes in samples collected from patients before, during and after immunotherapy. Our overarching objective is to characterize mechanisms of resistance to immunotherapy in CNS metastases. To achieve this, we will chart the co-evolution of cancer and the immune system over time and anatomical location

during immunotherapy by profiling DNA and RNA from cancer tissues, peripheral blood, and cerebrospinal fluid (CSF). Notably, using cutting edge single-cell technologies, we will examine alterations to the cancer genome and immune cell behaviors at unprecedented resolution. Furthermore, in our innovative mouse models of brain

metastases, we will study novel combination therapies, including CDK inhibition with immune-checkpoint blockade, to augment the efficacy of immunotherapy. We believe that this work has the potential to uncover basic mechanisms of treatment-failure in these patients and that these discoveries will have tremendous translational

potential as a basis on which to refine existing immunotherapy protocols and develop novel treatment strategies.

All Grantees

Massachusetts General Hospital

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