1. Targeted therapies prime oncogene-driven lung cancers for macrophage-mediated destruction
- Author
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Vaccaro, Kyle, Allen, Juliet, Whitfield, Troy W., Maoz, Asaf, Reeves, Sarah, Velarde, Jose, Yang, Dian, Meglan, Anna, Ribeiro, Juliano, Blandin, Jasmine, Phan, Nicole, Bell, George W., Hata, Aaron N., and Weiskopf, Kipp
- Subjects
Diagnosis ,Drug therapy ,Testing ,Physiological aspects ,Genetic aspects ,Dosage and administration ,Health aspects ,Lung cancer -- Diagnosis -- Genetic aspects -- Drug therapy ,Macrophages -- Physiological aspects -- Health aspects ,Oncogenes -- Health aspects ,Immune checkpoint inhibitors -- Dosage and administration -- Testing - Abstract
Introduction Many cancers arise from a single mutation in a proto-oncogene that drives tumor growth. These cancers are often treated with genotype-directed 'targeted therapies,' small-molecule inhibitors that specifically disable growth [...], Macrophage immune checkpoint inhibitors, such as anti-CD47 antibodies, show promise in clinical trials for solid and hematologic malignancies. However, the best strategies to use these therapies remain unknown, and ongoing studies suggest they may be most effective when used in combination with other anticancer agents. Here, we developed an unbiased, high-throughput screening platform to identify drugs that render lung cancer cells more vulnerable to macrophage attack, and we found that therapeutic synergy exists between genotype-directed therapies and anti-CD47 antibodies. In validation studies, we found that the combination of genotype- directed therapies and CD47 blockade elicited robust phagocytosis and eliminated persister cells in vitro and maximized antitumor responses in vivo. Importantly, these findings broadly applied to lung cancers with various RTK/MAPK pathway alterations--including EGFR mutations, ALK fusions, or [KRAS.sup.G12C] mutations. We observed downregulation of [beta]2-microglobulin and CD73 as molecular mechanisms contributing to enhanced sensitivity to macrophage attack. Our findings demonstrate that dual inhibition of the RTK/MAPK pathway and the CD47/SIRPa axis is a promising immunotherapeutic strategy. Our study provides strong rationale for testing this therapeutic combination in patients with lung cancers bearing driver mutations.
- Published
- 2024
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