Talimogene Laherparepvec: Moving From First-In-Class to Best-In-Class.

Front Mol Biosci

Ankyra Therapeutics, Boston, MA, United States.

Published: February 2022

AI Article Synopsis

  • Talimogene laherparepvec (T-VEC) is a modified herpes simplex virus designed to treat melanoma by selectively targeting cancer cells and boosting the immune response through GM-CSF.
  • Approved by the FDA in 2015, T-VEC is specifically for patients with recurrent melanoma after initial surgery and represents the first oncolytic virus to receive such approval.
  • The review highlights the ongoing research for T-VEC’s effectiveness in non-melanoma cancers, clinical trial outcomes, identifying biomarkers for patient response, and future research directions to maximize the benefits of oncolytic virus therapies.

Article Abstract

Talimogene laherparepvec (T-VEC) is a modified oncolytic herpes Simplex virus, type 1 (HSV-1) encoding granulocyte-macrophage colony stimulating factor (GM-CSF). T-VEC is adapted for selective replication in melanoma cells and GM-CSF was expressed to augment host anti-tumor immunity. T-VEC is indicated for the local treatment of melanoma recurrent after primary surgery and is the first-in-class oncolytic virus to achieve approval by the FDA in 2015. This review will describe the progress made in advancing T-VEC to the most appropriate melanoma patients, expansion to patients with non-melanoma cancers and clinical trial results of T-VEC combination studies. Further, strategies to identify predictive biomarkers of therapeutic response to T-VEC will be discussed. Finally, a brief outline of high-priority future directions for investigation of T-VEC and other promising oncolytic viruses will set the stage for a best-in-class oncolytic virus to bring the maximum benefit of this emerging class of anti-cancer agents to patients with cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901478PMC
http://dx.doi.org/10.3389/fmolb.2022.834841DOI Listing

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