HSV-1 Oncolytic Viruses from Bench to Bedside: An Overview of Current Clinical Trials

Marilin S Koch1, Sean E Lawler1, E Antonio Chiocca1

  • 1Harvey Cushing Neurooncology Research Laboratories, Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

Cancers
|December 1, 2020
PubMed

Insights

Oncolytic Herpes simplex virus 1 (oHSV) therapies show promise in cancer treatment. Engineered oHSV variants are advancing in clinical trials, offering new oncology options with enhanced tumor targeting and immune response.

Area of Science:

  • Virology
  • Oncology
  • Immunotherapy

Background:

  • Herpes simplex virus 1 (HSV-1) serves as a genetic foundation for oncolytic viruses (OVs) in cancer therapy.
  • Engineered oHSV variants are designed to minimize neurotoxicity while maximizing anti-tumor effects and immune stimulation.
  • The FDA-approved oncolytic HSV-1, talimogene laherparepvec (T-VEC), highlights the clinical potential of this approach.

Purpose of the Study:

  • To review recent clinical trial outcomes for oncolytic HSV-1 therapies.
  • To provide an outlook on novel HSV-1 oncolytic variants under development.
  • To discuss advancements in tumor selectivity, replication efficiency, and immunostimulatory capacity of oHSV.

Main Methods:

  • Review of current clinical trial data for oncolytic HSV-1.
  • Analysis of newly developed HSV-1 oncolytic virus variants.
  • Assessment of tumor selectivity, replication, and immunostimulatory properties.

Main Results:

  • Several oHSV variants are in clinical trials, with some showing promising results.
  • Ongoing research focuses on enhancing oHSV's tumor-specific activity and immune-priming capabilities.
  • The landscape of oncologic therapies may expand with the successful development of new oHSV candidates.

Conclusions:

  • Oncolytic HSV-1 represents a significant area of development in cancer treatment.
  • Future oHSV variants aim for improved efficacy through enhanced tumor targeting and immunogenicity.
  • Clinical studies are crucial for validating the therapeutic potential of these advanced oncolytic viruses.

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