Abstract 3804: Engineering CAR macrophages in combination with anti-tumor therapies to suppress brain metastasis

Abstract Brain metastases pose a significant clinical challenge for patients with HER2-positive breast cancer, with up to 50% of those with metastatic disease developing CNS involvement. Although HER2-targeted therapies such as trastuzumab deruxtecan (T-DXd) have improved systemic outcomes, their limited penetration across the blood-brain barrier (BBB) leaves the brain as a sanctuary site for recurrence. Innovative strategies are urgently needed to overcome BBB restrictions and effectively treat HER2-positive brain metastases.To address this, we leveraged the unique ability of macrophages to cross the BBB and perform phagocytic and immune-modulatory functions. We engineered chimeric antigen receptor macrophages (CARMA) to express tumor antigen-specific scFv and activate down-stream signaling to enhance anti-tumor immunity. We hypothesize that CARMA can penetrate the BBB, exert potent anti-tumor activity, and synergize with tumor antigen-targeted therapy and T-DXd to improve outcomes in brain metastases. In preclinical models, CARMA demonstrated strong antigen-specific phagocytosis and significant suppression of brain metastases. Notably, CARMA exhibited minimal neurotoxicity compared to CAR-T cells and induced a bystander killing effect mediated by cytokines upregulation upon tumor antigen engagement.To further enhance efficacy, we evaluated a combination strategy of CARMA and T-DXd to synergize antibody-dependent cellular cytotoxicity (ADCC) with macrophage-mediated phagocytosis. Our results showed that this combination dramatically suppressed brain metastases. These findings position CARMA as a promising immunotherapy platform for HER2-positive breast cancer brain metastases, offering potential to overcome BBB limitations and improve patient outcomes through multi-modal synergy. Citation Format: Shih-Ying Wu, Abhishek Tyagi, Eleanor Cecile Smith, Ravindra Pramod Deshpande, Jee Won Kim, Kounosuke Watabe. Engineering CAR macrophages in combination with anti-tumor therapies to suppress brain metastasis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3804.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-3804
Primary Topic
Brain Metastases and Treatment
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article
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article

Abstract 3804: Engineering CAR macrophages in combination with anti-tumor therapies to suppress brain metastasis

Shih-Ying Wu, Jee Won Kim, Ravindra Pramod Deshpande, Eleanor Cecile Smith et al.
Cancer Research
Brain Metastases and Treatment
article

Abstract 3804: Engineering CAR macrophages in combination with anti-tumor therapies to suppress brain metastasis

Shih-Ying Wu, Jee Won Kim, Ravindra Pramod Deshpande, Eleanor Cecile Smith, Abhishek Tyagi, Kounosuke Watabe
article en

Abstract

Abstract Brain metastases pose a significant clinical challenge for patients with HER2-positive breast cancer, with up to 50% of those with metastatic disease developing CNS involvement. Although HER2-targeted therapies such as trastuzumab deruxtecan (T-DXd) have improved systemic outcomes, their limited penetration across the blood-brain barrier (BBB) leaves the brain as a sanctuary site for recurrence. Innovative strategies are urgently needed to overcome BBB restrictions and effectively treat HER2-positive brain metastases.To address this, we leveraged the unique ability of macrophages to cross the BBB and perform phagocytic and immune-modulatory functions. We engineered chimeric antigen receptor macrophages (CARMA) to express tumor antigen-specific scFv and activate down-stream signaling to enhance anti-tumor immunity. We hypothesize that CARMA can penetrate the BBB, exert potent anti-tumor activity, and synergize with tumor antigen-targeted therapy and T-DXd to improve outcomes in brain metastases. In preclinical models, CARMA demonstrated strong antigen-specific phagocytosis and significant suppression of brain metastases. Notably, CARMA exhibited minimal neurotoxicity compared to CAR-T cells and induced a bystander killing effect mediated by cytokines upregulation upon tumor antigen engagement.To further enhance efficacy, we evaluated a combination strategy of CARMA and T-DXd to synergize antibody-dependent cellular cytotoxicity (ADCC) with macrophage-mediated phagocytosis. Our results showed that this combination dramatically suppressed brain metastases. These findings position CARMA as a promising immunotherapy platform for HER2-positive breast cancer brain metastases, offering potential to overcome BBB limitations and improve patient outcomes through multi-modal synergy. Citation Format: Shih-Ying Wu, Abhishek Tyagi, Eleanor Cecile Smith, Ravindra Pramod Deshpande, Jee Won Kim, Kounosuke Watabe. Engineering CAR macrophages in combination with anti-tumor therapies to suppress brain metastasis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3804.

Cancer ResearchVol. 86(7_Supplement)
Wake Forest University (US)
Openalex Percentile: Top 26%
Brain Metastases and Treatment
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