Bexmarilimab-induced macrophage activation leads to treatment benefit in solid tumors: The phase I/II first-in-human MATINS trial

  • Jenna H. Rannikko
  • , Loic Verlingue
  • , Maria de Miguel
  • , Annika Pasanen
  • , Debbie Robbrecht
  • , Tanja Skytta
  • , Sanna Iivanainen
  • , Shishir Shetty
  • , Yuk Ting Ma
  • , Donna M. Graham
  • , Sukeshi Patel Arora
  • , Panu Jaakkola
  • , Christina Yap
  • , Yujuan Xiang
  • , Jami Mandelin
  • , Matti K. Karvonen
  • , Juho Jalkanen
  • , Sinem Karaman
  • , Jussi P. Koivunen
  • , Anna Minchom
  • Maija Hollmén, Petri Bono

Producción científica: Articlerevisión exhaustiva

27 Citas (Scopus)

Resumen

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.

Idioma originalEnglish (US)
Número de artículo101307
PublicaciónCell Reports Medicine
Volumen4
N.º12
DOI
EstadoPublished - dic 19 2023
Publicado de forma externa

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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