Communications Medicine (May 2024)

Phase 1 dose expansion and biomarker study assessing first-in-class tumor microenvironment modulator VT1021 in patients with advanced solid tumors

  • Jian Jenny Chen,
  • Melanie Y. Vincent,
  • Dale Shepard,
  • David Peereboom,
  • Devalingam Mahalingam,
  • James Battiste,
  • Manish R. Patel,
  • Dejan Juric,
  • Patrick Y. Wen,
  • Andrea Bullock,
  • Jennifer Eva Selfridge,
  • Shubham Pant,
  • Joyce Liu,
  • Wendy Li,
  • Susanne Fyfe,
  • Suming Wang,
  • Victor Zota,
  • James Mahoney,
  • Randolph S. Watnick,
  • Michael Cieslewicz,
  • Jing Watnick

DOI
https://doi.org/10.1038/s43856-024-00520-z
Journal volume & issue
Vol. 4, no. 1
pp. 1 – 15

Abstract

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Abstract Background Preclinical studies have demonstrated that VT1021, a first-in-class therapeutic agent, inhibits tumor growth via stimulation of thrombospondin-1 (TSP-1) and reprograms the tumor microenvironment. We recently reported data from the dose escalation part of a phase I study of VT1021 in solid tumors. Here, we report findings from the dose expansion phase of the same study. Methods We analyzed the safety and tolerability, clinical response, and biomarker profile of VT1021 in the expansion portion of the phase I study (NCT03364400). Safety/tolerability is determined by adverse events related to the treatment. Clinical response is determined by RECIST v1.1 and iRECIST. Biomarkers are measured by multiplexed ion beam imaging and enzyme-linked immunoassay (ELISA). Results First, we report the safety and tolerability data as the primary outcome of this study. Adverse events (AE) suspected to be related to the study treatment (RTEAEs) are mostly grade 1–2. There are no grade 4 or 5 adverse events. VT1021 is safe and well tolerated in patients with solid tumors in this study. We report clinical responses as a secondary efficacy outcome. VT1021 demonstrates promising single-agent clinical activity in recurrent GBM (rGBM) in this study. Among 22 patients with rGBM, the overall disease control rate (DCR) is 45% (95% confidence interval, 0.24-0.67). Finally, we report the exploratory outcomes of this study. We show the clinical confirmation of TSP-1 induction and TME remodeling by VT1021. Our biomarker analysis identifies several plasmatic cytokines as potential biomarkers for future clinical studies. Conclusions VT1021 is safe and well-tolerated in patients with solid tumors in a phase I expansion study. VT1021 has advanced to a phase II/III clinical study in glioblastoma (NCT03970447).