Neoadjuvant oncolytic virotherapy before surgery sensitizes triple-negative breast cancer to immune checkpoint

Marie-Claude Bourgeois-Daigneault1,2, Dominic Guy Roy3,2, Amelia Sadie Aitken3,2

  • 1Centre for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa K1H 8L6, Canada. mbourgeois@ohri.ca jbell@ohri.ca.

Insights

Early oncolytic virus (OV) therapy combined with surgery offers long-term benefits for triple-negative breast cancer (TNBC). OV treatment sensitizes TNBC to immune checkpoint inhibitors, preventing disease relapse in preclinical models.

Area of Science:

  • Oncology
  • Virology
  • Immunotherapy

Background:

  • Triple-negative breast cancer (TNBC) presents limited therapeutic options and severe toxicities.
  • Current immune checkpoint inhibitor (ICI) trials show limited success in TNBC, with responders often having pre-existing anticancer immunity.

Purpose of the Study:

  • To investigate oncolytic viruses (OVs) as a strategy to sensitize TNBC to ICIs.
  • To evaluate the efficacy of early OV treatment combined with surgical resection in a TNBC model.

Main Methods:

  • Utilized a therapeutic preclinical model simulating neoadjuvant treatment for newly diagnosed TNBC.
  • Administered oncolytic virus (OV) therapy in conjunction with surgical resection.
  • Assessed the impact of OV therapy on TNBC response to immune checkpoint blockade (ICB).

Main Results:

  • Early OV treatment followed by surgical resection demonstrated long-term survival benefits.
  • OV therapy successfully sensitized refractory TNBC to ICB.
  • Combination therapy prevented relapse in the majority of treated animals.

Conclusions:

  • Oncolytic virus therapy can enhance the efficacy of immune checkpoint inhibitors in triple-negative breast cancer.
  • The combination of OV and ICB warrants investigation as a neoadjuvant treatment strategy for TNBC.
  • This approach may be beneficial in the time interval between TNBC diagnosis and surgical resection.

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