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A link between osteoporosis treatment and breast cancer

MUHC-led study shows treatment has protective effect on bone metastasis
Published: 3 October 2014

Treatment approaches to reduce the risk of bone complications (metastasis) associated with breast cancer may be one step closer to becoming a reality. According to a study led by a team at the Research Institute of the ۲ݮƵ University Health Centre (RI-MUHC), findings show that medication used to treat bone deterioration in post-menopausal women may also slow skeletal metastasis caused from breast cancer. This study, published in this month’s issue of the Journal of the National Cancer Institute (JNCI), is among the first to link bisphosphonate (a common osteoporosis medication) use with improved survival in women with breast cancer.

“Skeletal metastases develop in up to 70 percent of women who die from breast cancer,” says study co-lead author, Dr. Richard Kremer, director of the Bone and Mineral Unit at the MUHC and a professor in the Faculty of Medicine at ۲ݮƵ University. “This causes considerable suffering and is life-threatening. Preventing this could translate into saving a significant number of lives.”

Reduction of metastatic risk by half

Dr. Kremer and co-lead author, Dr. Nancy Mayo, worked with colleagues to evaluate data from more than 21,000 women diagnosed with breast cancer. The relationship between use of oral bisphosphonates and development of bone metastases after diagnosis with breast cancer was evaluated in two groups of women: those with early stage, localized, cancer and those whose cancer had spread to lymph nodes. Their findings showed that women with early stage breast cancer who had taken oral bisphosphonates, either before or after diagnosis of their cancer, had a reduced risk of bone metastasis. In addition, their study showed that women with later stage cancer, who took oral bisphosphonates post-diagnosis, also had a significantly reduced risk of bone metastasis.

The researchers also established a dose-response relationship with oral bisphophonate use in women with local disease: longer time spent on bisphophonate medication resulted in a greater reduction of bone metastases.

“Our study is novel in that it mainly involved women who were post-menopausal and in whom bone-turnover is high due to osteoporosis,” says Dr. Richard Kremer who is also an RI-MUHC researcher. “We believe that this process results in an environment that is favorable for tumour cell growth and consequent metastasis. We know that bisphosphonates work by slowing down this bone-turnover. This will, in turn, make it harder for tumour cells to establish in the bone and may explain why we saw such a decline in metastasis.”

Clinical studies needed

“An association between bisphophonate use and improved survival was also observed and this merits further investigation,” Dr. Mayo, RI-MUHC researcher and James ۲ݮƵ professor in the Faculty of Medicine, School of Physical and Occupational Therapy at ۲ݮƵ. “Ours was an epidemiological study, involving a large number of women strengthening the importance of the findings. However, clinical interventional studies are needed before the results can be translated into standard clinical practice and guidelines.”

About the study:

This research was made possible thanks to funding from the Canadian Institutes of Health Research (CIHR), the Canadian Breast Cancer Research Initiative, the Quebec Network for Research on Drug Use , the Fonds de recherche du Québec - Santé (FRQS) and the Susan G. Komen Foundation

The paper Effects of oral bisphosphonates for osteoporosis on development of skeletal metastases in women with breast cancer: Results from a pharmaco-epidemiological study was co-authored by Richard Kremer, Department of Medicine, ۲ݮƵ University Health Centre (MUHC), Montreal, QC; Bruno Gagnon, Division of Clinical Epidemiology, MUHC, Montreal, QC and Centre de Recherche sur le Cancer, Université Laval, Quebec City, QC; Ari N. Meguerditchian, Department of Surgery, MUHC, Montreal, QC; Lyne Nadeau, Division of Clinical Epidemiology, MUHC, Montreal, QC; and Nancy Mayo, Department of Medicine and Division of Clinical Epidemiology, MUHC, Montreal, QC.

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