Angiosarcomas are highly lethal tumors that can occur in any part of the body. The tumor typically appears as a growth or lesion on the skin; the larger the growth, the greater the risk of mortality.
In 2014, Brad Bryan, Ph.D, an assistant professor at TTUHSC El Paso’s Center of Emphasis in Cancer, and William Chow, D.O., a dermatological oncologist at Mohs Micrographic Surgery and Cutaneous Oncology, treated a man with an enlarging lesion on his left cheek, forehead and scalp. Biopsy revealed it was angiosarcoma, and the case didn’t look good.
“We were presented with a patient exhibiting a rapidly expanding uniformly fatal tumor with no realistic options for a favorable outcome based on current standard treatments,” the two researchers wrote in their study.
Previous research in Bryan’s lab suggested that propranolol — a drug that’s typically used for high blood pressure — might be effective against angiosarcomas, so Chow and Bryan proceeded to use the medication to treat the patient.
After one week of the propranolol treatment, the tumor ceased its rapid expansion and showed no evidence of clinical enlargement or extension. Within six months of use of propranolol — and eventually, added chemotherapy and radiation — the patient’s tumor was undetectable. The results are published in the journal JAMA Dermatology.
The finding is not only promising against cancer, but for patient finances. Current prescription drug therapies for sarcomas can cost patients more than $10,000 a month. Propranolol, however, costs about $4 a month.
“If this finding extends to a broader patient population, administration of propranolol may be a major advancement in the treatment of angiosarcomas,” Bryan and Chow write.
Source: Texas Tech University Health Sciences Center El Paso