Macrophage Clever-1 contributes to impaired antigen presentation and suppression of anti-tumor immunity. This first-in-human trial investigates the safety and tolerability of Clever-1 blockade with bexmarilimab in patients with treatment-refractory solid tumors and assesses preliminary anti-tumor efficacy, pharmacodynamics, and immunologic correlates. Bexmarilimab shows no dose-limiting toxicities in part I (n = 30) and no additional safety signals in part II (n = 108). Disease control (DC) rates of 25%-40% are observed in cutaneous melanoma, gastric, hepatocellular, estrogen receptor-positive breast, and biliary tract cancers. DC associates with improved survival in a landmark analysis and correlates with high pre-treatment intratumoral Clever-1 positivity and increasing on-treatment serum interferon γ (IFNγ) levels. Spatial transcriptomics profiling of DC and non-DC tumors demonstrates bexmarilimab-induced macrophage activation and stimulation of IFNγ and T cell receptor signaling selectively in DC patients. These data suggest that bexmarilimab therapy is well tolerated and show that macrophage targeting can promote immune activation and tumor control in late-stage cancer.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10772343PMC
http://dx.doi.org/10.1016/j.xcrm.2023.101307DOI Listing

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Macrophage Clever-1 contributes to impaired antigen presentation and suppression of anti-tumor immunity. This first-in-human trial investigates the safety and tolerability of Clever-1 blockade with bexmarilimab in patients with treatment-refractory solid tumors and assesses preliminary anti-tumor efficacy, pharmacodynamics, and immunologic correlates. Bexmarilimab shows no dose-limiting toxicities in part I (n = 30) and no additional safety signals in part II (n = 108).

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Article Synopsis
  • Immune checkpoint inhibitors (ICIs) work better in inflamed tumors with T-cell infiltration and IFN signaling compared to cold tumors, which often resist treatment.
  • The cancer immunotherapy drug bexmarilimab helps activate immune responses by blocking a specific receptor that suppresses macrophages, showing potential benefits for advanced solid tumors.
  • Research using single-cell RNA sequencing on ovarian cancer macrophages revealed that bexmarilimab is most effective in those with low baseline IFN signaling, suggesting strategies to enhance responses in cold tumors.
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