WASHINGTONPerjeta may become the first pharmaceutical treatment approved to treat early-stage breast cancer before surgery.
Scientists from the Food and Drug Administration (FDA) have issued a positive review of Roche's breast cancer drug. Documents posted online say that women with early-stage breast cancer who received Perjeta (Pertuzimab) had significantly fewer tumors than women who received older drug combinations.
While the results come from mid-stage trials of the drug, FDA scientists recommended accelerating approval of the drug -- a step reserved for groundbreaking drugs to treat life-threatening diseases.
, late-stage breast cancer that has already spread to other parts of the body. But Roche's Genentech unit is now seeking approval to use the drug at a much earlier stage of the disease: after diagnosis and before tumor-removal surgery.
The FDA is scheduled to make a decision on whether to approve Perjeta for early-stage breast cancer by Oct. 31.
"This is tremendously exciting," Dr. Amy Tiersten, an associate professor in the division of hematology and medical oncology at Mt. Sinai Medical Center in New York City, said in an email to CBSNews.com. "The really exciting information is when (the late-stage effects of the drug) can be translated into earlier stages of disease where we can completely eradicate the disease and cure more women"
Breast cancer is the second deadliest form of cancer in U.S. women, and is expected to kill more than 39,000 Americans this year, according to the National Cancer Institute. More than 232,000 women are expected to be diagnosed with the disease during that time.
Surgery to remove tumors is the first-line treatment for virtually all forms of cancer. If approved, Perjeta would be the first cancer drug approved for use as a pre-surgical step. Early-stage cancer drugs are still experimental, but doctors hope the approach could help shrink tumors to make them easier to remove, or eliminate the need for surgery altogether.
On Thursday, the FDA will ask an outside panel of cancer specialists whether Perjeta's benefits outweigh its risks for treating early-stage breast cancer. Among other questions, the experts will be asked whether the preliminary results reported by Genentech are likely to result in longer overall survival for patients. The government agency isn't required to follow the panel's advice, though it often does.
The panel will review a 417-woman study comparing Perjeta in different combinations against older breast cancer treatments. When Perjeta was combined with Herceptin, another Genentech drug, and standard chemotherapy, 39 percent of women saw their cancer reach undetectable levels. Only 21 percent of women experienced the same results from taking Herceptin and chemotherapy .
Last year the FDA released guidelines for studying breast cancer drugs in the pre-surgical setting, with the aim of accelerating approval of promising therapies. Perjeta is the first drug to undergo FDA review since those recommendations were released. If approved, it could encourage more drugmakers to study cancer drugs for early-stage use.
"Despite advances in systemic therapy of breast cancer, there remains a need to expedite drug development and approval of highly effective therapies for patients with high-risk early-stage breast cancer," the FDA states in its review.
Like Herceptin, Perjeta only works in a subset of about 20 percent of breast cancer patients who carry a more aggressive form of the disease. These women have tumors that overproduce a protein known as HER-2 which makes cancer cells rapidly divide and grow.
FDA scientists stress in their review that Genentech's results are preliminary and will have to be confirmed in future trials. The company only measured the patients' immediate response to the drug, and did not submit follow-up data showing whether the cancer returned or whether women ultimately lived longer. But agency scientists said the company's approach "is reasonably likely to predict clinical benefit," and noted that Genentech is already enrolling patients in a late-stage trial that could confirm the results.
Since the early 1990s the FDA has granted accelerated approval to dozens of drugs based on promising early results, on the condition that their effectiveness is confirmed in later studies. That policy has been praised by patients with HIV, cancer and other deadly diseases where access to experimental treatments can mean life or death.
But the flipside of the program means removing drugs from the market if their initial promise isn't confirmed by later studies. The FDA was criticized in 2011 by some cancer patients when it r
The FDA concluded that the drug did not help breast cancer patients live longer or bring enough other benefit to outweigh its dangerous side effects. The drug is still approved to treat colon cancer and other forms of the disease.