Design of a single-center, phase II trial to explore the efficacy and safety of 'R-ISV-RO' treatment in advanced tumors

Future Oncol. 2024;20(17):1139-1149. doi: 10.2217/fon-2023-0962. Epub 2024 Mar 6.

Abstract

Background: The authors' preclinical study has confirmed that RO adjuvant (composed of TLR 7 agonists [imiquimod/R837] and OX40 agonists) injected into local lesions induces the regression of both primary tumor and distant metastasis. The authors propose to realize local control and exert abscopal effect through an 'R-ISV-RO' in situ strategy plus anti-PD-1 monoclonal antibody in advanced tumors. Methods: This study is a single-center, exploratory, phase II trial to evaluate the efficacy and safety of R-ISV-RO plus anti-PD-1 monoclonal antibody in advanced tumors. 30 patients with one or more measurable extracerebral lesions that are accessible for radiation or injection will be enrolled. The primary endpoint is the objective response rate of target lesions. Discussion/Conclusion: The efficacy and safety of the novel strategy will be further validated through this clinical trial.Clinical trial registration: ChiCTR2100053870 (www.chictr.org.cn/).

Keywords: OX40 agonist; immuno-microenvironment; in situ immune; intratumoral injection; tumor vaccines.

Plain language summary

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Publication types

  • Clinical Trial Protocol

MeSH terms

  • Adult
  • Aged
  • Clinical Trials, Phase II as Topic
  • Female
  • Humans
  • Imidazoles / administration & dosage
  • Imidazoles / therapeutic use
  • Male
  • Middle Aged
  • Neoplasms* / drug therapy
  • Neoplasms* / pathology
  • Oncolytic Virotherapy / adverse effects
  • Oncolytic Virotherapy / methods
  • Treatment Outcome

Substances

  • Imidazoles
  • resiquimod