- MONDAY, May 5 (HealthDay News) — In women who have been diagnosed with
breast cancer, having a known mutation in the BRCA 1 or 2 genes raises the
risk of a second cancer, and many of these women choose to have their
second breast removed before that has a chance to happen.
However, new research suggests that women who don't have these
genetic mutations may still face an increased risk of a second cancer,
especially if they have a family history of breast cancer or atypical
breast cells.
The study involved women with a family history of breast cancer,
although only some had a BRCA mutation. The researchers found that the
risk of cancer in the second breast was about 10 percent, regardless of
whether the woman carried a BRCA mutation or not.
The findings were slated to be presented Sunday at the American Society
of Breast Surgeons' annual meeting, in New York City.
The study suggests that “we may not have identified all of the genes
associated with breast cancer,” according to study author Dr. Shawna
Willey, director of the Betty Lou Ourisman Breast Health Center at the
Lombardi Cancer Center at Georgetown University in Washington D.C.
Many high-risk women may not be advised to have a prophylactic
mastectomy even though it could be potentially lifesaving, she added.
“Having a prophylactic mastectomy should not be a knee-jerk reaction to
a diagnosis of breast cancer. Women need to consider this data, as well as
other data, and decide whether or not this is a measure they want to
take,” advised Willey. She said the findings may also add to the debate
about which breast cancer patients should have sentinel lymph node
biopsies.
“Prevention of secondary breast cancer is becoming increasingly
important,” said Dr. Julia Smith, director of the Lynne Cohen Breast
Cancer Preventative Care Program at the New York University Cancer
Institute in New York City. “Because of advances in treatment, it's
possible that many younger women with breast cancer may live for decades,
so we have to focus on what we can do to prevent a further problem.”
And, she said, many of the effective chemotherapy drugs can't be used a
second time because they may be too toxic to healthy cells if given
repeatedly, and cancer cells can become resistant to some forms of
chemotherapy.
“We use our best treatment at the time to try to ensure long-term
survival, but if another breast cancer comes along, we may be limited,”
she said.
While women with BRCA mutations are known to have a higher risk of
developing an additional cancer, Willey and her colleagues wanted to learn
if women with a family history but no known BRCA mutations carried a
similar risk.
The analysis included 119 women who were part of the Familial Cancer
Registry. All of the women had been diagnosed with an initial breast
cancer, and had decided to prophylactically remove the second breast.
When the researchers analyzed the breast tissue from the second breast,
they found cancer about 10 percent of the time, regardless of whether or
not a woman had a BRCA mutation.
If the normal breast cancer cells were atypical — meaning they showed
precancerous changes — the risk of breast cancer jumped to about 50
percent over a lifetime for a woman with a family history of the disease,
according to Willey.
“Not having a BRCA mutation doesn't let you off the hook,” Smith
noted.
“There's no question that family history is extremely important. Even
without a BRCA mutation, we counsel women to consider prophylactic
mastectomy if they have a strong family history,” she added.
More information
To learn more about prophylactic mastectomy, visit the National Cancer Institute.
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