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Hormone Replacement Therapy Litigation
Hormone Replacement Therapy ("HRT") places women at a higher
risk for breast cancer, ovarian cancer, lupus, heart attack, stroke, gall
bladder cancer, asthma, and other serious illnesses, according to recent
studies.
If you have develped any of these serious illnesses, please call us or
e-mail our law firm by submitting a Potential
Case Form to learn more about your legal rights concerning HRT.
Prempro, Premarin, Provera, Premphase, Estradiol, and Medroxyprogesterone
are commonly prescribed hormone replacement drugs.
If you or a loved one has been diagnosed with breast cancer, ovarian cancer,
or with any other female cancer, and if you have ever regularly used hormone
replacement drugs for menopause, there is a good chance that the hormones
fed your cancer. We thought you might be interested in some of the recent
studies.
Breast Cancer
Breast cancer is not a single disease. There are many different kinds
of breast tumors. Hormone therapy has been associated with two types in
particular: invasive (or infiltrating) lobular cancer, and estrogen receptor
positive invasive ductal cancer.
The Women's Health Initiative Trial was halted in July 2002 because, among
other reasons, Prempro was causing an unacceptable increase in breast
cancer. Since then, there have been six major studies on the risk of breast
cancer from hormone therapy on a total of more than 11,200 women with
breast cancer. They have all found that combination hormone therapy is
strongly associated with two particular types of breast cancer. What follows
is a brief summary of these six studies.
1. Tjonneland et al., "HRT in Relation to Breast Carcinoma Incidence
Rate Ratios", Cancer (June 1, 2004) 100(11), 2329-37. Women on hormone
therapy developed more than twice as many ductal breast cancers and almost
four times as many lobular breast cancers as women not taking those drugs.
In this large prospective case control study in Denmark, funded by the
Danish Cancer Institute, 29,000 women were followed for six years.
2. Holmberg et al., "HABITS (HRT after breast cancer---is it safe?),
a randomised comparison: trial stopped", Lancet, Feb 3 2004 363:453-455.
This was a randomized trial in Sweden to see if breast cancer survivors
could safely use hormone therapy. The trial was halted halfway through
it because the women on hormones were getting almost three times as much
of breast cancer recurrence as the placebo group not on the hormones.
It found almost a five-fold increased risk of hormone receptor positive
breast cancers.
3. Stahlberg et al., "Increased Risk of Breast Cancer Following Different
Regimens of HRT Frequently Used in Europe", Int J Cancer 109, 721-27
(2004). This is a study of breast cancer in Danish nurses, followed over
time. Women taking combination hormone therapy (an estrogen plus a progestin)
developed three times as much breast cancer as the other groups.
4. Verkoouen et al., "Important Increase of lobular breast cancer
incidence in Geneva Switzerland", Int. J. Cancer, 104, 778-81 (2003).
The rates of different types of breast cancer were tracked over 25 years
in Geneva, where both the rate of breast cancer and the use of hormone
therapy in menopause are the highest in the world. The study found a dramatic
seven-fold increase in the amount of invasive lobular breast cancer in
the women with the highest use of hormone drugs.
5. Million Women Study Collaborators, "Breast Cancer and hrt in the
Million Women Study", Lancent Aug 9 2003, 362, pp 419-427. This is
by far the largest study of women with breast cancer and hormone therapy.
See their website, http://www.millionwomenstudy.org.uk. Funded by the
British government, the investigators are following over 1,300,000 post-menopausal
women in the UK for years to come. In the first but not last report on
breast cancer, they found after only a two and a half year average follow-up
that twice as many women on combination therapy were getting breast cancer,
without distinguishing between different types of tumors (that project
is underway and will be published in a year or so). The study investigators
estimated that hormone therapy had caused over 20,000 excess cases if
breast cancer in the UK alone, and just in women 50-65 in the last ten
years.
6. Li, et al. "Relationship Between Long Durations and Different
Regimens of HT and Risk of Breast Cancer," JAMA, 289(24), 3254-63.
This is a large case control study funded by the US National Cancer Institute
that focused on women in the Seattle area. In 975 women with breast cancer,
they found that the risk was tripled for lobular breast cancer and doubled
for estrogen positive and progesterone positive tumors of all types in
women who had ever used combination hormone therapy in menopause.
Ovarian Cancer
As for ovarian cancer, there have been several large studies published
in the last few years that confirm a causal association between hormone
therapy and ovarian cancer, especially in long time users of estrogen
only, and especially for some types of ovarian cancer tumors and not for
others. Just like breast cancer, ovarian cancer is not just one disease,
but a name for a widely different group of tumors that all happen to grow
in the ovaries. The three largest studies published to date are as follows:
1. The largest single study is from Australia: Purdie et al.:"Hormone
replacement therapy and risk of epithelial ovarian cancer", Br. J.
of Cancer (1999)81(3), 559-563. In this study on 973 women with ovarian
cancer, they found that unopposed estrogen hormone therapy was associated
with a significant increase in risk of endometrioid or clear cell epithelial
ovarian tumors (OR=2.56, upper confid. interval 4.94) in all women. But
in women without a hysterectomy, that is, in women who still had their
uterus, and who also did not have a tubal ligation, then all forms of
ovarian cancer were increased significantly; such women on estrogen only
therapy were four times as likely to develop ovarian cancer as never users.
The risk went up steadily with length of use of the hormone drugs.
2. The second largest case control study, with 655 cases of invasive ovarian
cancer, is from Sweden. See Riman et al., “Hormone replacement therapy
and the risk of invasive epithelial ovarian cancer in Swedish women”,
J Natl Cancer Inst 2002;94:467-504. This study also found a statistically
significant increase in ovarian cancers, sometimes a tripling of the risk,
especially of the tumor types endometrioid and mucinous, in women on most
forms of hormone therapy.
3. The third recent big case control study was done by the National Cancer
Institute. Lacey et al., "Menopausal HRT and Risk of Ovarian Cancer",
JAMA, July 17, 2002, 288(3), 334-341. This study looked at 329 ovarian
cancer cases at 29 sites across the United States. This study mostly confirmed
the Australian study: they found the risk to be mostly with estrogen-only
hormone drugs; that the rate of increased risk varied by type of ovarian
tumor; and that women without hysterectomies were at a much higher risk
of a hormone drug induced tumor. They also found that the risk increased
with the length of use of the hormone drugs. The risk was tripled for
women on estrogen for over twenty years.
The Million Women Study has not reported any data on ovarian cancer yet.
The Women's Health Initiative combination therapy trial found an elevation
in risk, but it was not statistically significant (the study is much smaller
than the three described above; it had only 32 women with ovarian cancer,
and they were followed for only 5 years, so there was not the time nor
the numbers to see the effects on tumor types and duration seen in the
larger studies.). See Anderson et al., "Effects of Estrogen Plus
Progestin on Gynecologic Cancers and Associated Diagnostic Procedures",
JAMA, Oct 1, 2003 290(13), 1739-1748.
The WHI estrogen only arm has not published any data on ovarian cancer.
However, since all the women in that study had hysterectomies, and the
study followed them for only about 7 years, and because it is too small
to see increases in rare cancers, it is not likely to provide any information
that would change the picture given by the three major case control studies
described above.
If you have been injured, it is important to have an Washington attorney
evaluate any personal injury claim you may have. The law provides strict
deadlines for bringing personal injury claims. It is critical that you
contact an Washington injury attorney if you think that you may have a claim.
A Washington personal injury attorney at Vangelisti Law Offices can provide
you a free consultation to discuss your injuries and legal rights.
If you have a potential hormone replacement therapy case in Oregon, please visit our sister-site at http://www.vangelisti.com/practice_areas/hormone_replacement.htm.
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