FDA Approves Groundbreaking New Cancer Treatment That Gives Tumors a Killer Case of Herpes
By engineering viruses to hunt down malignant cells, researchers hope they can spare patients the painful side effects of chemotherapy.
Image via (cc) Flickr user Oriol Salvador
In what’s being called a major advance toward “a complete change in the game,” the FDA has for the first time given the green light to a new form of cancer treatment—one that researchers hope might someday make chemotherapy, and its adverse side effects, a thing of the past.
The key, as it turns out, is viruses—more specifically, herpes.
Last week the FDA announced its approval of a “genetically modified live oncolytic herpes virus therapy” in which viruses are engineered specifically to hunt and kill the malignant cells associated with the skin cancer melanoma. The treatment—talimogene laherparepvec (“T-VEC”)—will be sold under the brand name Imlygic by BioVex Inc. and its parent company, Amgen. This is reportedly the first instance of a viral cancer treatment’s approval by the agency. Explains an FDA release:
Image via (cc) Flickr user mr_d_logan
Imlygic [...] is used to treat melanoma lesions that cannot be removed completely by surgery. Imlygic is injected directly into the melanoma lesions, where it replicates inside cancer cells and causes the cells to rupture and die.
A treatment course with Imlygic consists of a series of injections into the melanoma lesions. After the initial injection, a second dose is administered three weeks later, followed by additional doses every two weeks for at least six months, unless other treatment is required or until there are no remaining injectable lesions to treat.
What makes this particular herpes virus special is its unique genetic engineering, which causes it to infect malignant cells while ostensibly avoiding healthy ones. In other words, it targets cancer, with minimal risk of giving a patient herpes, as we commonly know it (although, the FDA warns, some risk still remains for those with suppressed immune systems, or women who are pregnant). And while the agency does list several other potential side effects, such as fever, chills, and “flu-like symptoms,” these seem mild compared to the draining effect of current cancer treatments.
An article published this past May in the Journal of Clinical Oncology describes the results of a large round of clinical testing of the procedure. It concludes that using the modified herpes virus did, in fact, shrink tumors and afford patients a marginally longer lifespan. The results weren’t groundbreaking—this is a treatment, and not a cure—but as the study’s authors write, “T-VEC represents a novel potential therapy for patients with metastatic melanoma.”
Beyond melanoma, however, researchers see the FDA’s approval of Imlygic as an important milestone when it comes to using smart viruses to treat other forms of cancer. Ultimately, the goal for many physicians is to end the need for physically—and oftentimes psychologically—trying therapies such as chemo or radiation. As Mayo Clinic oncolytic virotherapy researcher Dr. Stephen Russell explained to The Guardian, the FDA’s approval of Imlygic opens the door to further research into the use of viruses to target diseased cells. He says: “We can’t prematurely claim that we’ve achieved our ultimate goal, because we haven’t; this really is a single step along that path. But it’s a very important and very significant step.”
Herpes, as it turns out, could someday help save your life.