CSF-1R Inhibitor Development: Current Clinical Status

  • Curr Oncol Rep. 2017 Sep 5;19(11):70. doi: 10.1007/s11912-017-0634-1.
Florent Peyraud  1  2 Sophie Cousin  1  2 Antoine Italiano  3  4
Affiliations
  • 1. Early Phase Trials Unit, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France.
  • 2. Department of Medicine, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France.
  • 3. Early Phase Trials Unit, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France. [email protected].
  • 4. Department of Medicine, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France. [email protected].
Abstract

Purpose of review: Colony-stimulating factor 1 receptor (CSF-1R) and its ligands, CSF-1 and interleukin 34 (IL-34), regulate the function and survival of tumor-associated macrophages, which are involved in tumorigenesis and in the suppression of antitumor immunity. Moreover, the CSF-1R/CSF-1 axis has been implicated in the pathogenesis of pigmented villonodular synovitis (PVNS), a benign tumor of the synovium. As advanced or metastatic malignant solid tumors and relapsed/refractory PVNS remain unresolved therapeutic problems, new approaches are needed to improve the outcome of patients with these conditions.

Recent findings: In solid tumors, targeting CSF-1R via either small molecules or antibodies has shown interesting results in vitro but limited antitumor activity in vivo. Concerning PVNS, clinical trials assessing CSF-1R inhibitors have revealed promising initial outcomes. Blocking CSF-1/CSF-1R signaling represents a promising immunotherapy approach and several new potential combination therapies for future clinical testing.

Keywords
CSF-1; CSF-1R inhibitor; CSF1-R; Diffuse-type giant-cell tumor; Pigmented villonodular synovitis; Solid tumors; Targeted therapy; Tumor-associated macrophages.
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