http://news.yahoo.com/novartis-drug-may-help-older-breast-cancer-patients-1206STOCKHOLM (Reuters) - Novartis's bone drug Zometa extended survival in older breast cancer patients but failed to improve disease-free survival among younger women patients in a large-scale clinical trial, researchers said on Sunday.
Detailed data presented at the  European Multidisciplinary Cancer Congress (EMCC) in Stockholm showed  that Zometa, a bisphosphonate drug known generically as zoledronic acid,  only improved overall survival rates in patients who had undergone the  menopause at least five years earlier.
Researchers said the effect was  likely to be linked to levels of reproductive hormones, which are lower  in women who have been through the menopause.
"This is not a treatment for ever  woman with breast cancer," said Robert Coleman of Britain's Sheffield  University, who led the study. But for women with low levels of female  hormones, either due to aging or specific treatments to induce  menopause, Zometa "appears very promising."
An analysis of the subset of older  patients showed that at a the five-year follow-up, there was a 26  percent reduction in recurrence of tumors, Coleman said, as well as a 26  percent reduction in the risk of an early death.
These strong results could lead to "a major new treatment approach" for post-menopausal patients, he said.
Zometa, which generated sales of  $2.1 billion for Novartis in 2010, is an intravenous drug from a widely  used class of osteoporosis medicines called bisphosphonates.
It is increasingly being prescribed  to help reduce or delay fractures and other skeletal complications in a  variety of cancers that have spread to the bones. From 65 to 75 percent  of breast cancer recurrences occur in the bones.
This trial, called AZURE and also  published in the New England Journal of Medicine on Sunday, involved  3,360 women with early-stage breast cancer from 174 centers in Britain,  Australia, Spain, Ireland, Portugal, Taiwan and Thailand.
Patients randomly allocated receive  standard chemotherapy and/or hormone therapy, either with or without  the addition of Zometa, a drug that works by inhibiting the cells that  break down bone, called osteoclasts.
The results showed that looking  across all trial participants, there was no significant difference in  disease-free survival or overall survival between patients who received  Zometa and those who didn't. But in a subset of older patients, the  addition of the Novartis drug did bring clear benefits.
These women, who had at least five  years since their last period, had an overall survival rate at five  years of 85 percent on Zometa compared with 79 percent for those not on  the drug. For all other patients, overall five-year survival was  similar, at 86 percent in the Zometa group and 85 percent in the control  group.
Investigators said that most  surprising among the findings was the drug's effect on the rate at which  the cancer recurred outside the bone. The relative risk for developing  metastases, or secondary tumors, outside bone during treatment with  Zometa was approximately halved in the postmenopausal women compared  with the younger patients.
Coleman said the results shed new light on the role bones may play in the progress of the disease.
"The effects on metastasis and  recurrence outside bone suggests that the bone marrow is an important  sanctuary for tumor cells which can be activated after, sometimes, many  years of dormancy," he said. "With help from bone marrow stem cells,  they may then spread via the blood stream to set up metastases at other  sites."