Pilot study of oncolytic viral therapy using mutant herpes simplex virus (HF10) against recurrent metastatic breast

Hideto Kimata1, Tsuneo Imai, Toyone Kikumori

  • 1Department of Surgery II, Graduate School of Medicine, Nagoya University, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

Abstract

Insights

Oncolytic herpes simplex virus type 1 mutant (HF10) showed safety and efficacy in a pilot study for metastatic breast cancer. Intratumoral injection led to significant cancer cell death with no adverse effects observed.

Area of Science:

  • Virology
  • Oncology
  • Immunology

Background:

  • Oncolytic herpes simplex virus type 1 mutant (HF10) demonstrates antitumor efficacy in preclinical models.
  • HF10 has shown effectiveness and safety against various non-neuronal malignant tumors in animal studies.
  • Previous research indicates HF10 can confer resistance to tumor rechallenge in surviving mice.

Purpose of the Study:

  • To evaluate the safety and efficacy of HF10 in patients with metastatic breast cancer.
  • To assess local and systemic adverse effects following intratumoral HF10 injection.
  • To determine the impact of HF10 on cancer cell death in human tumors.

Main Methods:

  • A pilot study involved six patients with cutaneous or subcutaneous breast cancer metastases.
  • HF10 suspension was injected into one tumor nodule, with sterile saline injected into a control nodule per patient.
  • Patients were monitored for adverse effects, and nodules were excised 14 days post-injection for histopathology.

Main Results:

  • Intratumoral injection of HF10 was well-tolerated by all patients.
  • No local or systemic adverse effects were reported.
  • Histopathological analysis revealed cancer cell death ranging from 30% to 100% in HF10-treated nodules.

Conclusions:

  • HF10 is a safe and effective agent for treating metastatic breast cancer.
  • Intratumoral HF10 demonstrates significant oncolytic activity in human tumors.
  • This pilot study supports further investigation of HF10 in breast cancer therapy.