Oncolytic HSV and cancer drug interactions: Current clinical status and future directions

Karina Vázquez-Arreguín1, Kimberly A Rivera-Caraballo2, Divya Ventarapragada3

  • 1Department of Pathology, Medical College of Georgia and Georgia Cancer Center, Augusta University, Augusta, GA 30912, USA.

Insights

Oncolytic herpes simplex viruses (oHSVs) are engineered viruses that kill tumor cells and stimulate anti-tumor immunity. Ongoing clinical trials explore combinations of these viruses with drugs to enhance cancer treatment efficacy.

Area of Science:

  • Oncology
  • Virology
  • Immunotherapy

Background:

  • Oncolytic herpes simplex viruses (oHSVs) are engineered viruses designed for targeted tumor cell destruction and immune stimulation.
  • Current oHSV therapies include Imlygic for melanoma and Delytact for brain tumors, with ongoing development of second-generation viruses.

Purpose of the Study:

  • To summarize the current landscape of oHSVs in cancer therapy.
  • To review the rationale and mechanisms behind virus-drug combinations in clinical trials.
  • To detail the design principles of oHSVs and their interactions with antineoplastic therapeutics.

Main Methods:

  • Review of existing literature on oHSV development and clinical trials.
  • Analysis of preclinical data on virus-drug interactions.
  • Summary of ongoing clinical investigations for various malignancies.

Main Results:

  • Second-generation oHSVs are being developed to enhance tumor cell killing and immune response.
  • Numerous preclinical studies suggest synergistic interactions between oHSVs and various drugs.
  • Over 100 clinical trials are evaluating oHSVs as monotherapy or in combination treatments.

Conclusions:

  • oHSVs represent a promising biotherapy for various cancers, with significant potential when combined with other therapeutics.
  • Understanding virus-drug interactions is crucial for optimizing oHSV-based cancer treatment strategies.
  • The extensive clinical trial landscape indicates a strong focus on advancing oHSV therapies for improved patient outcomes.

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