Dec. 9, 2010 (San Antonio) -- Postmenopausal women with early breast cancer who take newer hormone drugs known as aromatase inhibitors are 26% more likely to develop heart disease than those who take the old standby tamoxifen, researchers report.
"Treatment with aromatase inhibitors is associated with a significant increase in the risk of cardiovascular events, specifically heart attacks, angina, and heart failure, compared with tamoxifen," says Eitan Amir, MD, a senior fellow in oncology and hematology at the Princess Margaret Hospital in Toronto.
However, the actual risk of any individual woman developing heart problems was relatively small -- about 4% -- in women taking either aromatase inhibitors or tamoxifen, he says.
In fact, the analysis showed that 132 patients must be treated with an aromatase inhibitor before one cardiovascular problem occurs. "This number needed to harm is relatively high," Amir says.
But a woman who already has risk factors for heart disease and takes an aromatase inhibitor has a 7% chance of developing heart problems, Amir tells WebMD.
For the study, Amir polled the results of seven trials of tamoxifen and aromatase inhibitors involving nearly 30,000 postmenopausal women with early breast cancer.
The study was presented at the San Antonio Breast Cancer Symposium.
Tamoxifen, which blocks estrogen from getting into cancer cells, slowing tumor growth, has been used for decades to treat breast cancer.
In recent years, its use has been largely supplanted by aromatase inhibitors, which actually shut down the body's ability to make estrogen.
Aromatase Inhibitors vs. Tamoxifen: What Should Women Do?
The findings suggest that women at risk for heart disease should limit use of aromatase inhibitors, Amir says.
"Starting with tamoxifen and then switching to an aromatase inhibitor after several years -- rather than starting with an aromatase inhibitor and staying on it -- may reduce the risk of dying from causes other than breastcancer," he says. "But this is just a hypothesis at this point."
An expert who worked on the landmark ATAC study that first showed the effectiveness of aromatase inhibitors disagrees.