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Risk factors and causes
Scientists continue to study the genes responsible for
familial ovarian cancer. This research is beginning to yield clues
about how these genes normally work and how disrupting their action can
lead to cancer. This information eventually is expected to lead to new
drugs for preventing and treating familial ovarian cancer.
Research in this area has already led to better ways to detect
high-risk genes and assess a woman's ovarian cancer risk. A better
understanding of how genetic and hormonal factors (such as oral
contraceptive use) interact may also lead to better ways to prevent
ovarian cancer.
Prevention
New information about how much BRCA1 and BRCA2 gene mutations
increase ovarian cancer risk is helping women make practical decisions
about prevention. For example, mathematical models have been developed
that help estimate how many years of life an average woman with a BRCA
mutation might gain by having both ovaries and fallopian tubes removed
to prevent a cancer from developing. A recent study showed that
fallopian tube cancers develop in women with BRCA gene mutations more
often than doctors had previously suspected. However, it is important
to remember that although doctors can predict the average outcome of a
group of many women, it is still impossible to accurately predict the
outcome for any individual woman.
Other studies are testing new drugs for ovarian cancer risk
reduction
Researchers are constantly looking for clues such as
lifestyle, diet, and medicines that may alter the risk of ovarian
cancer.
Early detection
Accurate methods for detecting ovarian cancer early could have
a great impact on the cure rate. Researchers are testing new ways to
screen women for ovarian cancer, and a national repository for blood
and tissue samples from ovarian cancer patients is being established to
aid in these studies. One method being tested is looking at the pattern
of proteins in the blood (called proteomics) to find ovarian cancer
early.
From time to time, lab companies have marketed unproven tests
to look for early ovarian cancer. Because these tests had not yet been
shown to help find early cancer, the FDA told the companies to stop
selling them. So far, this occurred with 2 different tests looking at
protein patterns: OvaSure and OvaCheck. Both were taken off the market
at the request of the FDA.
Two large studies of screening have recently been completed.
One was in the United States, and the other was in the United Kingdom.
Both studies looked at using the CA-125 blood test along with ovarian
(transvaginal) ultrasound to find ovarian cancer. These studies have
found early cancers in some women. But it is not known whether the
outcomes of these women have been improved compared with women who
haven't undergone screening.
Diagnosis
A new test called OVA1 has recently been approved by the FDA.
It measures the levels of 4 proteins in the blood of women who have an
ovarian tumor. The levels of these proteins, when looked at together,
are used to put women with tumors into 2 categories -- low risk and
high risk. The women who are labeled low risk are not likely to have
their tumor be cancer. The women who are called high risk are more
likely to have a cancer, and so should have surgery performed by a
specialist (a gynecologic oncologist). This test is NOT a screening
test - it is only meant for use in women who have an ovarian tumor.
Treatment
Treatment research includes testing the value of currently
available methods as well as developing new approaches to treatment.
New chemotherapy combinations that may help cancers resistant
to current treatments are constantly being investigated.
For cancers to grow, blood vessels must develop to nourish the
cancer cells. This process is called angiogenesis. Drugs have been
developed that are useful in stopping cancer growth by preventing new
blood vessels from forming. One drug, called bevacizumab (Avastin) has
been able to shrink or slow the growth of advanced ovarian cancers.
Trials to see if bevacizumab works even better when given along with
chemotherapy have shown good results in terms of shrinking (or stopping
the growth of) tumors. But there have been problems with patients
developing holes in the bowel wall (perforations) during treatment.
This complication can be fatal. Experts are still studying the safest
way to give this drug with other chemotherapy.
Other targeted therapies are being studied including
inhibitors of growth factors, which stimulate the growth of the cancer
cells.
Poly(ADP-ribose) polymerases (PARPs) are enzymes that have
been recently recognized as key regulators of cell survival and cell
death. Drugs that inhibit PARP-1 help fight cancers in caused by
mutations in BRCA1 and BRCA2. These drugs may make cancers in women
without BRCA mutations more sensitive to radiation therapy and some
kinds of chemotherapy (methylating agents and topoisomerase I
inhibitors). Clinical trials are in progress to determine whether these
drugs will improve outcomes for ovarian cancers that develop in women
without BRCA mutations.
Another approach is to develop tumor vaccines that program the
immune system to better recognize cancer cells. Also, antibodies that
specifically recognize and attack ovarian cancer cells are being
developed. Perhaps some or all of these approaches along with
chemotherapy will lead to cures for this disease.
Consolidation therapy -- treatment following first line
therapy to prevent recurrence -- is undergoing clinical trials. Some of
these trials are using chemotherapy, growth factor inhibitors and
monoclonal antibodies. Monoclonal antibodies are like the antibodies
our bodies make to fight infection. These, however, are made in the
laboratory and are directed against specific sites on the cancer cell.
Studies are on-going.
Last Medical Review: 08/27/2009 Last Revised: 08/27/2009
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