[YOUR HEALTH] Drug may extend survival for men with cancer

A new hormone therapy drug for men with prostate cancer may increase survival a bit and delay progression of the disease in men who have advanced prostate cancer that has been resistant to standard hormonal therapies, a new study suggests.

The study found that the drug enzalutamide increased survival by 29 per cent and delayed disease progression by 81 per cent in men who hadn’t received any treatment with chemotherapy.

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“There’s new hope for men with very advanced prostate cancer,” said study author Dr. Tomasz Beer, deputy director of the Knight Cancer Institute at Oregon Health and Science University in Portland.

“This is a treatment with an excellent safety profile that can help men maintain quality of life and extend disease-free progression and extend survival.”

The findings are scheduled to be presented at a meeting of the American Society of Clinical Oncologists, in San Francisco.

The study authors reported receiving research funding from the drug’s manufacturers.

The US Food and Drug Administration approved enzalutamide in 2012 for use in men with advanced prostate cancer who have received chemotherapy.

The drug is a type of hormone therapy called an androgen receptor blocker. Androgens are male hormones.

Enzalutamide is considered a second-generation hormone therapy. First-generation hormone therapy drugs for prostate cancer include bicalutamide, flutamide and nilutamide.

The current study included more than 1,700 men with prostate cancer that had spread to other areas of their bodies.

The men’s cancer also had progressed despite treatment with other types of hormone therapy.

None of these men had yet been treated with chemotherapy. They had, however, been treated with surgery and radiation therapy.

Half of the volunteers were randomly assigned to receive enzalutamide and the other half received a placebo.

The study was stopped early because it was clear that enzalutamide offered a benefit over a placebo, so the drug was offered to all of the study volunteers.

“There was an 81 percent reduction in the risk of disease progression for men on enzalutamide,” Beer said.

“The median time to disease progression in placebo was [about four] months, but on the drug, a median time to disease progression hasn’t been reached despite 20 months of follow-up.”

When the study was stopped, 28 per cent of those on enzalutamide had died, compared with 35 per cent of those taking a placebo.

The average median survival rate at the time of the first analysis was 32.4 months for those on enzalutamide versus 30.2 months for those taking a placebo.

“This drug is being used relatively early in prostate cancer, and patients can receive multiple treatments after,” Beer said of the study population. Most of the men involved in the study were later treated with chemotherapy.

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