About 30 percent of people with SEGAs need surgery, but even in highly skilled hands, surgery to remove the tumors is risky, and if the operation doesn't get all the tumor tissue, the growths come back. The disorder also causes seizures in about 90 percent of patients.
Franz said about one-third of TS patients are severely affected and have a host of problems, including learning difficulties; about two-thirds are of normal intelligence.
Investigators from Cincinnati Children's Hospital decided to experiment with everolimus, a drug approved earlier for kidney cancer, because it inhibits a protein involved in both the growth of kidney cancer cells and SEGAs.
The study was an open-label trial, in which all patients received the medication. The participants, who had to be at least age 3, were mostly children and teens, with 22 younger than 18. There were 17 males and 11 females, whose average age was 11. Although the study initially was designed to last six months, investigators continued treating the patients and monitoring the sizes of their tumors using MRI. The mean treatment duration was 21.5 months.
The medication had secondary benefits for patients with seizures. In the 16 patients for whom researchers had 24-hour electroencephalograms recording brain waves, nine experienced fewer seizures while taking the medication. Seizures were unchanged in six patients; one experienced an increase in seizure frequency.
But the benefits of Afinitor come with serious side effects. Because the drug suppresses the immune system, it can make patients more prone to infections, and the FDA-approved patient information sheets warn of potential pneumonia or bacterial, fungal or viral infections.
Drug reactions reported by study participants included sinusitis, mouth ulcers and sores, and low white blood cells, as well as vomiting, dizziness, pneumonia, bronchitis and tooth infections.
Franz's study continues; he hopes to have five years of Afinitor data in tuberous sclerosis. Because so many of his clinical trial patients had fewer seizures on the pills, he's studying their potential in epilepsy patients.
He also said that some of the same pathways that are involved in TS are involved in many cancers and other diseases such as Alzheimer's, Parkinson's and Huntington's. What these all have in common is excessive accumulation of protein toxic to brain cells.
Franz also said he believes the drug could help with behavioral learning problems, because the same pathway is involved in "how you form memory and learning."
But, for now, while the drug is about to be marketed to patients with brain tumors, he and those who treat tuberous sclerosis patients are happy to offer a new treatment tool.
"It's not a cure," said Oakland's Brown, who is leading an advanced study of the drug, "but it's a very good treatment."