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FDA OKs Herpesvirus to Treat Cancer

The US Food and Drug Administration’s approval of an engineered herpesvirus for the treatment of melanoma marks the first oncolytic virus to enter the market.

Written byJef Akst
| 1 min read

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FLICKR, DOMINIC ALVES“The era of the oncolytic virus is probably here,” Stephen Russell, a cancer researcher and haematologist at the Mayo Clinic in Rochester, Minnesota, told Nature.

Yesterday (October 27), the US Food and Drug Administration (FDA) greenlighted Amgen’s T-VEC (now called Imlygic), a genetically engineered herpesvirus called talimogene laherparepvec, for the treatment of melanoma lesions in the skin and lymph nodes, making it the first oncolytic virus to receive market approval. Dozens of other oncolytic viruses are currently being tested in clinical trials.

The therapy is based on a simple principle: many viruses will preferentially infect cancer cells and spur an immune reaction that will wipe out the diseased cells. But while this phenomenon has long been recognized (physicians made note of cancer patients who went into spontaneous remission after contracting a viral infection more than a century ago), it took decades of research to develop an effective and safe therapy. ...

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Meet the Author

  • Jef (an unusual nickname for Jennifer) got her master’s degree from Indiana University in April 2009 studying the mating behavior of seahorses. After four years of diving off the Gulf Coast of Tampa and performing behavioral experiments at the Tennessee Aquarium in Chattanooga, she left research to pursue a career in science writing. As The Scientist's managing editor, Jef edited features and oversaw the production of the TS Digest and quarterly print magazine. In 2022, her feature on uterus transplantation earned first place in the trade category of the Awards for Excellence in Health Care Journalism. She is a member of the National Association of Science Writers.

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