April 2, 2002
Hormone
Replacement, Cancer Studied
By THE ASSOCIATED PRESS
Filed at 4:01 p.m. ET
WASHINGTON (AP) -- A study shows a modest increased risk of ovarian
cancer among women who use some forms of hormone replacement therapy,
but researchers say the findings are not strong enough to recommend
changes.
In the study, which appeared Tuesday in the Journal of the National
Cancer Institute, Swedish researchers report that women using estrogen
replacement therapy had a 43 percent increased risk of ovarian cancer,
while those combining estrogen with sequential progestins had a 54
percent increased risk.
The authors, however, said that the results need to be verified by
other researchers and noted: ``We advocate cautious interpretations of
our results and do not recommend changes to current (hormone replacement
therapy) prescribing practices.''
In absolute numbers, the researchers said, the increased risk of
cancer was only modest. For every 1,000 women on hormone therapy, there
would be only two to three more cases of ovarian cancer, they said. In
Sweden, ovarian cancer is diagnosed in about 1 percent of women between
the ages of 50 and 75, irregardless of hormone therapy use, the authors
noted.
The study is the latest to raise questions about the common practice
of prescribing estrogen hormone supplements for women after menopause.
The hormones are taken by millions of women to combat hot flashes,
osteoporosis (the brittle bone disorder) and other complications of
menopause.
Recent studies have challenged the long-held belief that hormone
supplements ward off heart disease. Other research has linked the
hormone therapy to a slight increase in the risk of breast cancer. An
earlier study also linked the hormones to a modest increase in ovarian
cancer risk.
``These findings would not change the benefit-risk ratio for most
women,'' JoAnn E. Manson, the chief of preventative medicine at
Harvard's Brigham and Women's Hospital in Boston, said of the Swedish
study.
She said that clinical decisions about hormone replacement therapy
should be based on other factors, such as controlling hot flashes and
preventing the brittle bone disease.
``Short term use of hormone therapy for treatment of hot flashes
should not appreciably increase the risk of these cancers,'' Manson
said. ``We can still be reassuring to most women who use the therapy for
a short time.''
In the new study, eight researchers found 655 women on the Swedish
cancer registries who had epithelial ovarian cancer and 3,899
cancer-free women. The women were between the ages 50 and 74.
The researchers sent the women forms asking questions about their
history of HRT use and other factors that could affect their risk of
ovarian cancer.
By analyzing the responses, the researchers found that women who had
used estrogen alone were 43 percent more likely to have ovarian cancer
than women who did not use HRT. For women who used the estrogen therapy
along with the periodic use of progestins, another hormone, there was a
54 percent increased risk of ovarian cancer compared to HRT non-users.
However, for women who took estrogen pills combined with progestins
there was no increased risk of the disease.
Women who were on the therapy for 10 years or more had the greatest
risk of ovarian cancer, the study concluded.
The first author of the study is Dr. Tomas Riman of the department of
obstetrics and gynecology at Falu Hospital in Sweden.
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On the Net:
Journal of the National Cancer Institute:
http://www3.oup.co.uk/jnci/special/
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