Surg Clin N Am 88 (2008) 845861

Management of Women
Who Have a Genetic Predisposition
for Breast Cancer
Ismail Jatoi, MD, PhDa,*,
William F. Anderson, MD, MPHb
a

Breast Care Center, National Naval Medical Center, Uniformed Services University,
8901 Wisconsin Avenue, Bethesda, MD 20889, USA
b
Biostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer
Institute, National Institutes of Health, Department of Health and Human Services,
Bethesda, MD 20852, USA

Breast cancer is a major public health problem, aecting 12.3% or one in

eight of all women in the United States (123/1000 women) during their lifetime [1]. The three most important risk factors for breast cancer, in decreasing order of importance, are gender, aging, and family history [2]. Although
many women have no immediate family members who have had breast cancer, some clearly do. Since the nineteenth century, there have been numerous
reports of families suering from multiple cases of breast cancer. In 1866,
Paul Broca, a French surgeon, published the rst such description, reporting
that 10 of 24 women through ve successive generations of his wifes family
had died of breast cancer [3].
Approximately 5% to 10% of all breast cancers in the United States occur in women who have a genetic predisposition, and most of these are attributable to mutations in the breast cancer susceptibility gene 1 (BRCA1)
and breast cancer susceptibility gene 2 (BRCA2) [4,5]. Other genes also
are associated with breast cancer, including p53, PTEN, STK11/LKB1,
CDH 1, ATM, and CHEK 2 [6]. The lifetime risk of breast cancer

The views or opinions expressed in this article are those of the authors and should not
be construed as representing the official views of the Departments of the Army, Navy, or
Defense.
This research was supported in part by the Intramural Research Program of the National
Institutes of Health/National Cancer Institute.
* Corresponding author.
E-mail address: [email protected] (I. Jatoi).
0039-6109/08/$ - see front matter. Published by Elsevier Inc.
doi:10.1016/j.suc.2008.04.007

surgical.theclinics.com

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JATOI & ANDERSON

(penetrance) varies considerably among women who carry these mutations.

The high-penetrance mutations (eg, BRCA1, BRCA2, p53, PTEN, STK11/
LKB1, CDH1) are associated with a high lifetime risk of breast cancer
(40%85%), whereas the low-to-moderate penetrance mutations (eg,
ATM, CHEK 2) are associated with a lower risk [6]. These mutations are
associated with an increased risk for other cancers and diseases as well as
breast cancer. Thus, these mutations are linked with a diverse spectrum of
syndromes that includes the hereditary breast and ovarian cancer syndrome
(BRCA1 and BRCA2), Li-Fraumeni syndrome (p53), Cowdens disease
(PTEN), Peutz-Jeghers syndrome (STK11/LKB1), hereditary diuse gastric
carcinoma syndrome (CDH 1), ataxia-telangiectasia (ATM), and a LiFraumeni syndrome variant (CHEK 2) [6,7]. Many of these syndromes
are discussed in other articles in this issue. This article focuses on the hereditary breast and ovarian cancer syndromes, which are responsible for more
than half of the known cases of hereditary breast cancer. Much of the
discussion focuses on the management of breast cancer risk, but BRCA
mutation carriers also are at increased risk for ovarian cancer [8]. Therefore,
issues pertinent to the management of ovarian cancer risk in BRCA mutation carriers are discussed briey. Finally, issues relevant to breast cancer
treatment in mutation carriers are discussed.

Hereditary breast and ovarian cancer syndrome

BRCA1 and BRCA2 are tumor-suppressor genes, identied in chromosomes 17 and 13, respectively, coding for proteins intimately involved in
cellular growth and dierentiation [9,10]. In the United States approximately 1 woman in 250 carries a mutation in these genes, predisposing these
women to an increased risk for breast and ovarian cancer [11]. The BRCA1
and BRCA2 gene mutations are transmitted in an autosomal dominant
manner and therefore may originate from either the maternal or paternal
side [12]. Each ospring of a BRCA1 or BRCA2 mutation carrier has
a 50% chance of inheriting that mutation, and a carefully documented family history is essential for the initial assessment of any woman concerned
about a hereditary predisposition to breast cancer. If a woman has multiple
close relatives (mother, sisters, daughters, grandmothers, aunts) who have
had breast and ovarian cancer diagnosed at an early age (before age
50 years), close relatives who have had bilateral breast cancer, close male relatives (father, brothers, uncles, grandfathers, sons) who have had breast
cancer, and/or if the woman is of Ashkenazi Jewish ancestry, a hereditary
predisposition to breast cancer might be suspected [13]. Even in women
who have one or more of these risk factors, however, the likelihood of
a BRCA1 or BRCA2 mutation is quite low [14].
The BRCA1 and BRCA2 genes were cloned in 1994 and 1995, respectively, and genetic testing for breast cancer susceptibility was adopted widely

GENETIC PREDISPOSITION FOR BREAST CANCER

847

soon afterwards [15,16]. Numerous mutations now have been identied in

each of these genes, and dierent mutations within the same gene are associated with dierent risks for breast and ovarian cancer [12]. Among women
who have BRCA1 and BRCA2 mutations, the lifetime risk of breast cancer
is 36% to 85%, and the lifetime risk of ovarian cancer is 16% to 60%
[17,18]. These risk estimates, however, were derived from large families
with many aected members. Although family members share mutations
in the BRCA genes, they share other genes as well and often live in a similar
environment. Thus, these risk estimates partly reect the impact of other
genetic or environmental factors and may not indicate the risk of breast
and ovarian cancer among mutation carriers in the general population.
Also, risk estimates often were derived from families outside the United
States. Chen and colleagues [19] recently have estimated that, in the United
States population, the cumulative breast cancer risk by age 70 years for
BRCA1 and BRCA2 mutation carriers is 46% and 43%, respectively, and
the cumulative risk for ovarian cancer is 39% and 22% [19]. These estimates
point out that many women who have BRCA mutations never develop
breast or ovarian cancer.
Alterations in the BRCA1 or BRCA2 genes are more common in certain ethnic and geographic populations (eg, Ashkenazi Jewish, Norwegian, Dutch, Icelandic), and specic mutations (founder mutations)
often are clustered in particular ethnic groups [20]. For example, alterations in the BRCA1 or BRCA2 gene occur in approximately 2.5% of
individuals of Ashkenazi Jewish decent, and three specic mutations
(two in the BRCA1 gene and one in the BRCA2 gene) are ubiquitous
in these individuals [21]. The three founder mutations frequently observed
in persons of Ashkenazi Jewish heritage are 185delAG (BRCA1),
5383insC (BRCA1), and 617delT (BRCA2). The risk of breast cancer is
similar in carriers of the two founder BRCA1 gene mutations (approximately 65%) but is lower in carriers of the founder BRCA2 mutation
(43%) [22]. Individuals of Ashkenazi Jewish heritage should be tested
for all three founder mutations, because two or more may coexist in
the same family.
Clearly, women who have BRCA mutations have a markedly increased
risk of developing breast and ovarian cancer at an early age. Men who
have BRCA1 or BRCA2 mutations (particularly BRCA2) also are at increased risk for breast cancer, although that risk is considerably lower
than it is in women. Recently, it was estimated that the cumulative
risk, by age 70 years, of breast cancer is about 1.2% for male BRCA1
mutation carriers and about 6.8% for male BRCA2 mutation carriers
[23]. Carriers of the BRCA1 and BRCA2 mutations also are at increased
risk for other cancers, notably cancers of the prostate and pancreas [24].
Women who have a strong family history for breast cancer may consider
genetic testing, particularly if they wish to pursue strategies to lower their
risk.

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Genetic testing
Many organizations, including the US Preventive Services Task Force
(USPTF) and the American Society of Clinical Oncology, recommend
against genetic testing in women who have a low risk for the BRCA mutation [25,26]. In low-risk individuals, the potential risks of genetic testing outweigh the benets. For instance, in a woman without a family history of
breast cancer, how might one interpret an alteration in the BRCA gene
that never has been strongly linked to cancer? Such an alteration might be
less pathogenic than other mutations or even phenotypically silent. Thus,
indiscriminate genetic testing may produce needless anxiety and lead to
unnecessary prophylactic surgery or other treatments. Women might be
labeled falsely as having a genetic predisposition to breast cancer, with
adverse ethical, legal, nancial, and social consequences.
Over the years, a number of empiric models were developed to estimate
a womans risk of developing breast cancer (eg, the Gail, Claus, TyrerCuzick, and BRCAPRO models) [6]. There now are models that specically
estimate the likelihood for deleterious BRCA mutations (eg, the Myriad
Genetic Laboratories, Couch, BRCAPRO, and Tyrer models) [6,13]. These
models incorporate information about personal or family history of breast
and ovarian cancer as well as Ashkenazi Jewish background [27]. If a woman
has a 10% or greater probability of carrying a BRCA1 or BRCA2 gene mutation, genetic testing should be considered [28]. Informed consent should be
obtained before genetic testing, and the potential risks and benets should
be discussed in detail. Women should understand that the BRCA test is
predictive rather than diagnostic [29]. Diagnostic tests conrm the diagnosis of a particular condition (eg, an extra chromosome 21 in an infant
conrms the diagnosis of Downs syndrome), whereas predictive tests reveal
the likelihood of developing a particular disease (in this case, breast cancer)
but do not conrm that an individual will develop the disease.
The rst person tested for the BRCA mutation should be a family member most likely to test positive, generally an individual who has developed
breast cancer at a young age or an individual who has ovarian cancer
[27]. If a mutation is found in that family member, other members of the
family should be tested for the same mutation. In a family in which
a BRCA1 or BRCA2 mutation has been identied, individuals who do
not carry the mutation are not at increased risk for breast or ovarian cancer.
At worst, their risk is similar to that of the overall population, but it might
be even less, because risk estimates of the overall population include women
who carry the BRCA1 and BRCA2 mutations.
If a BRCA mutation is not found in a family member who has breast or
ovarian cancer, the test is not informative and does not provide useful information to other family members. In such instances, the cluster of breast cancer cases within a family might be attributable to mutations other than those
in the BRCA1 or BRCA2 genes or to environmental or lifestyle factors. If no

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GENETIC PREDISPOSITION FOR BREAST CANCER

family members who have cancer are alive or available for testing, the
options for testing should be weighed and considered on an individual basis.
Management options for mutation carriers
To reduce cancer-related mortality, women who have BRCA1 or BRCA2
mutations may wish to consider screening, chemoprevention, or prophylactic surgery (Fig. 1). The impact of these interventions on cancer-related
mortality is not understood fully, however, because no randomized, prospective trials have addressed their impact specically in mutation carriers.
The results of clinical trials indicate that breast cancer screening is benecial
in the overall population and that chemoprevention is useful in high-risk
populations. Additionally, the results of retrospective and nonrandomized
prospective studies indicate that these risk-reducing strategies benet mutation carriers.
Screening
There always has been a widespread belief that the early detection of cancer is benecial. For individuals at high risk for developing cancer, intensive
cancer screening often is recommended, even if proper evidence to support
such a recommendation is lacking. For example, it long was assumed that
screening with sputum cytology and/or chest radiographs would reduce
lung cancer mortality among smokers. Eventually, the results of four randomized, controlled trials proved this assumption wrong [30]. This example

Breast Screening
Mammography
CBE
MRI

Ovarian Screening
Transvaginal ultrasound
CA-125
pelvic exam

Management options
for women who carry
BRCA1 and BRCA 2
mutations

Prophylactic Surgery
Mastectomy
Salpingo-oophorectomy

Chemoprevention
Tamoxifen

Fig. 1. Management options for women who carry the BRCA1 or BRCA2 mutations.

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illustrates why the impact of screening on cancer-related mortality should be

ascertained through large, randomized, prospective trials whenever feasible.
Such trials, however, probably are not feasible in women who have a genetic
predisposition for breast cancer, so screening recommendations in these
women often are based on the results of randomized, controlled trials undertaken in the general population. Although other types of studies (eg, retrospective and case-control control) have been used to assess the ecacy of
screening, those studies have limitations, particularly in lead time, length,
and selection biases [30,31].
Survival refers to the interval of time from diagnosis of cancer to
death, and lead-time bias refers to the interval between the diagnosis
of cancer by screening and usual clinical detection [30,31]. As a result of
lead-time bias, one might conclude that screening improves survival,
when in fact it simply extends the period of time over which the cancer is
observed. The only way to exclude the eect of lead-time bias is to test
the ecacy of screening in a randomized, controlled trial, with mortality
as the end point. Thus, even though screening may result in the early detection of cancer, early detection alone never should justify its use. It is necessary to conduct randomized, controlled trials to prove that a particular
screening modality reduces mortality.
In addition to lead-time bias, retrospective studies are subject to length
bias and selection biases [30,31]. Length bias refers to the fact that slowergrowing cancers exist in the preclinical phase for a longer period of time and
therefore are more likely to be detected by screening. In contrast, fastergrowing tumors exist for a shorter period of time in the preclinical phase
and are more likely to be detected clinically in the intervals between screening sessions. Retrospective comparisons of screen-detected and clinically
detected cancers might reveal that screen-detected cancers have better outcomes, but this nding could reect, in part, the more indolent biology of
the screen-detected cancers. Thus, length bias reects the dierences in tumor biology between the screen-detected and clinically detected cancers.
There also are dierences in the characteristics of women who volunteer
for screening and those who do not; these dierences result in selection
bias. Women who volunteer for cancer screening generally are more health
conscious (eg, eat nutritional foods, exercise regularly) than those who
decline screening. As a result, women who volunteer for screening may
have better outcomes after a cancer diagnosis, and these outcomes might
be attributable in part to their lifestyle.
The only way to exclude lead-time, length, and selection biases is to conduct randomized, prospective trials with mortality as the end point. For
breast cancer, ve screening modalities commonly are considered: mammography, ultrasound, MRI, clinical breast examination (CBE), and breast
self-examination (BSE) (screening CBE diers from screening BSE in that it
requires the use of trained personnel) [3032]. Nine randomized, prospective
trials have assessed the impact of mammography screening (with or without

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851

CBE) on breast cancer mortality in the general population: the Health

Insurance Plan (HIP) of New York, Malmo, Two-County, Stockholm,
Gothenburg, Edinburgh, Canadian National Breast Screening Study I
(CNBSS I), Canadian National Breast Screening Study II (CNBSS II),
and Age Trials [30,31,33]. Currently, a trial is underway in India to assess
the impact of screening CBE alone in the general population [31]. Additionally, two trials, conducted in St. Petersburg, Russia, and in Shanghai, China,
have assessed the impact of screening BSE on breast cancer mortality in the
general population [34,35]. To date, no randomized, prospective trials have
assessed the impact of ultrasound or MRI screening on breast cancer mortality. At least six nonrandomized prospective studies have shown that in
high-risk patients MRI is more sensitive than mammography [36], but no
randomized, prospective trials have assessed the impact of any of these
screening modalities specically in mutation carriers.
Several overviews (meta-analyses) of the mammography screening trials
have been published [37,38]. These meta-analyses indicate that, in the general population, the impact of screening diers in younger and older women.
For women who are over the age of 50 years at the start of these trials, a signicant 20% to 25% reduction in breast cancer mortality is attributable to
screening, evident after 7 to 9 years of follow-up. In contrast, for women
below age 50 years at the start of these trials, the benet of mammography
screening emerges gradually, with a signicant reduction in mortality (about
18%) appearing after 12 or more years of follow-up. These meta-analyses
did not include the results of the Age trial, the most recent randomized clinical trial to examine the ecacy of screening mammography in women aged
40 to 49 years [33]. This trial showed that breast cancer deaths in the
screened group were decreased, but that decrease did not reach statistical
signicance (relative risk, 0.83; 95% condence interval [CI], 0.661.04).
Although mammography screening seems to be ecacious in the general
population, its impact on mutation carriers is not known. Some investigators have suggested that, because the BRCA1 and BRCA2 genes code for
proteins involved in DNA repair, low-dose radiation from mammography
might be particularly detrimental in mutation carriers, potentially increasing
their risk for breast cancer [39]. Additional data are needed to determine if
this concern is valid, but recent studies seem to indicate that it is not [40,41].
To date, no randomized, controlled trials have compared CBE screening
alone with no screening, although four of the nine mammography screening
trials (HIP, Edinburgh, CNBSS I, CNBSS II) also included CBE as a screening modality [31]. The results of these four trials suggest that screening CBE
can detect cancers eectively, and Barton and colleagues [42] estimate that
screening CBE has a sensitivity of approximately 54% and a specicity of
about 94%. Additionally, two randomized, controlled trials have examined
the eect of screening BSE alone on breast cancer mortality in the general
population [34,35]. The rst of these trials conducted by the World Health
Organization recruited women between the years 1985 and 1989 in

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St. Petersburg, Russia. The other was initiated between the years 1989 and
1991 in Shanghai, China. In the control and study arms of these trials,
breast cancer detection and mortality rates were nearly identical, but the
number of breast biopsies performed was nearly twofold higher in the
screened group. Thus, false-positive results are common with BSE screening
and may lead to unnecessary biopsies.
At least six prospective, nonrandomized studies have evaluated annual
MRI screening (in conjunction with mammography) in women at increased
risk for developing breast cancer (Fig. 2) [36]. These studies were conducted
in the United States, the Netherlands, Canada, the United Kingdom, Germany, and Italy, and participants either were documented BRCA1 or
BRCA2 mutation carriers or had a very strong family history of breast cancer. In some of these studies, ultrasound and/or CBE also were used as
screening modalities. The sensitivity of MRI ranged from 77% to 100%,
whereas the sensitivity of mammography or ultrasound was only 16% to
40%. There are, however, no data from randomized prospective trials to indicate whether the improved detection rates associated with MRI screening
translate to a reduction in breast cancer mortality. Although MRI is more
sensitive than mammography, its specicity is lower. Kriege and colleagues
[43] found that the specicity of MRI was 88%, compared with 95% for
mammography. The lower specicity of MRI leads to higher recall and
false-positive rates. The danger of false-positive screening results is unnecessary biopsies.
As mentioned earlier, evidence concerning the ecacy of breast cancer
screening is derived from trials undertaken in the general population. To
date, no randomized clinical trials have been designed to assess the benet

Fig. 2. Breast cancer (arrow) detected on screening MRI.

GENETIC PREDISPOSITION FOR BREAST CANCER

853

of these screening modalities in mutation carriers. Nonetheless, several organizations have published screening guidelines for women who have a hereditary predisposition for breast cancer. The National Comprehensive Cancer
Network recommends monthly BSE starting at age 18 years, CBE every
6 months starting at age 25 years, annual mammography starting at age
25 years, and annual breast MRI starting at age 25 years [6]. The American
Cancer Society recommends annual BSE and annual breast MRI [44], beginning at age 30 years and continuing for as long as a woman is in good
health. The USPTF, however, maintains that there is insucient evidence
at the present time to recommend for or against breast cancer screening
in mutation carriers [26]. Given the uncertainty surrounding the ecacy
of breast cancer screening among mutation carriers, it seems prudent to discuss its potential for benet and harm with each patient.
BRCA mutation carriers also are at considerable risk for developing
ovarian cancer. As yet, no data from randomized clinical trials (either in
the general population or in high-risk women) indicate whether ovarian cancer screening reduces cancer-related mortality. Furthermore, there are no
reliable methods for detecting ovarian cancer early. Nonetheless, a number
of screening tests have been investigated for potential use, particularly the
serum marker CA-125 and transvaginal ultrasound [45]. CA-125 is a protein
produced by more than 90% of advanced epithelial ovarian cancers. Transvaginal ultrasound is the most promising imaging method for the early
detection of ovarian cancer. Combining transvaginal ultrasound and CA125 results in a higher sensitivity for ovarian cancer detection than either
method alone but increases false-positive rates. Although BRCA mutation
carriers generally have been urged to undergo screening with transvaginal
ultrasound and CA-125, a recent study suggests that this screening may
not detect tumors at a suciently early stage to inuence prognosis [46].
Prophylactic surgery
To reduce cancer risk, BRCA1 and BRCA2 mutation carriers may wish
to consider prophylactic surgery. These patients are at increased risk both
for breast and ovarian tumors and for tumors arising from the fallopian
tubes [47]. Thus, BRCA mutation carriers should consider prophylactic
mastectomy and prophylactic salpingo-oophorectomy (rather than
oophorectomy alone). Patients concerned about the potential impact of
prophylactic mastectomy on body image may elect to undergo salpingooophorectomy alone because it is a hidden procedure and may reduce
the risk of both ovarian and breast cancer risk. These patients generally
opt for continued surveillance of the breasts. Alternatively, nulliparous
women may consider prophylactic mastectomy initially and delay salpingo-oophorectomy until after childbearing. Again, no randomized, prospective trials have assessed the impact of these procedures, although the
results of several retrospective studies indicate that they dramatically reduce

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cancer risk. Patients should be made aware that these procedures do not
eliminate cancer risk entirely.
Hartmann and colleagues [48] conducted a retrospective analysis of
women who had a family history of breast cancer and who underwent
prophylactic mastectomy at the Mayo Clinic between 1960 and 1993. To estimate the number of breast cancers expected in the absence of prophylactic
mastectomy, the authors applied the Gail model for women at moderate
risk. For women at high risk, the authors compared those who underwent
prophylactic mastectomy with their sisters who did not. In this study, prophylactic mastectomy reduced the incidence of breast cancer by 90%, and
other studies have shown similar results [4951].
Three procedures are used commonly for prophylactic mastectomy: total,
skin-sparing, and subcutaneous (nipple-sparing) mastectomy (Table 1) [47].
Total mastectomy involves removal of the breast tissue, nipple, areola, and
much of the skin overlying the breast. In contrast, skin-sparing mastectomy
involves removal of the breast tissue, nipple, and areola, but preserves skin
overlying the breast. Skin-sparing mastectomy facilitates breast reconstruction and results in a better cosmetic outcome than total mastectomy [52].
The reduction in breast cancer risk seems to be similar for total mastectomy
and skin-sparing mastectomy. Subcutaneous mastectomy, which involves
removal of the breast tissue but leaves the nipple and areola intact, seems
to be less eective [47].
Breast reconstruction usually is undertaken at the time of prophylactic
mastectomy. Reconstruction is feasible with either prostheses alone or autogenous tissue (with or without prostheses) [53]. If a patient opts for prosthesis alone, the prosthesis generally is placed below the pectoralis major
muscle at the time of mastectomy. Alternatively, an expander can be placed
and inated gradually over a period of several weeks by injecting solution
through a port. This process creates a ptosis, and the injectable port and
expander subsequently are removed and replaced with a permanent prosthesis. In some instances, the expander is left in place as the permanent prosthesis. If the patient chooses reconstruction with autogenous tissue, then either
a latissimus dorsi ap or the transverse rectus abdominis muscle (TRAM)
ap might be considered [54]. The latissimus dorsi ap does not provide sufcient tissue bulk, and a prosthesis usually is placed beneath the ap. The

Table 1
Types of prophylactic mastectomy
Procedure

Description of procedure

Recommendation

Skin-sparing mastectomy
Total mastectomy

Removal of breast, nipple, areola

Removal of breast, nipple, areola,
and skin overlying breast
Removal of breast; preserves
nipple and areola

Preferred
Acceptable

Subcutaneous mastectomy

Not recommended

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855

TRAM ap provides considerable tissue bulk, and a prosthesis usually is

not required. Although it might result in an aesthetically more appealing
outcome, the TRAM procedure is technically more challenging and carries
a greater risk of complications.
Among BRCA mutation carriers, the risk of ovarian cancer is considerably less than that of breast cancer. There are, however, no reliable means
of detecting ovarian cancer early, and it is more lethal than breast cancer.
Thus, mutation carriers often are urged to undergo bilateral salpingooophorectomy after completion of childbearing. Kau and colleagues [55]
and Rebbeck and colleagues [28] reported that prophylactic surgery (either
salpingo-oophorectomy or oophorectomy) reduces the risk of ovarian cancer by about 90% in mutation carriers. Additionally, premenopausal
oophorectomy in mutation carriers was associated with about a 50% reduction in breast cancer risk [28,55]. After removal of the ovaries, BRCA
mutation carriers still are at small risk for developing papillary serous carcinoma of the peritoneum, so continued surveillance is warranted.
Chemoprevention
Tamoxifen is a selective estrogen-receptor modulator widely used in the
treatment of estrogen receptorpositive breast cancers [56]. More than
20 years ago, Cuzick and Baum [57] reviewed the results of women who
received tamoxifen following surgery for breast cancer and found that it reduced the risk of contralateral breast cancer. This observation led to the
hypothesis that tamoxifen could prevent breast cancer, and four randomized, prospective trials were initiated to test this hypothesis. These trials
were the Royal Marsden trial [58], the National Surgical Adjuvant Breast
and Bowel Project (NSABP) P-1 trial [59], the Italian trial [60], and the International Breast Intervention Study-1 trial [61], all of which assigned
women randomly to receive either tamoxifen (20 mg daily) or placebo for
at least 5 years. An overview of these trials showed that the administration
of tamoxifen reduced the risk of invasive breast cancer by about 38% (95%
CI, 28%46%; P ! .0001) [62]. Tamoxifen now is approved as a chemopreventive agent for women at high risk for breast cancer.
No randomized, prospective trial has tested the impact of tamoxifen
specically in BRCA mutation carriers, although each of the four trials mentioned earlier undoubtedly included women who had BRCA mutations. A
subgroup analysis of the NSABP P-1 trial failed to show a signicant benet
of tamoxifen in preventing breast cancers in BRCA mutation carriers, but
such a benet could not be excluded completely [63]. A case-control study,
however, did nd that tamoxifen was eective in preventing breast cancer in
BRCA mutation carriers. In that study, Narod and colleagues [64] compared
BRCA mutation carriers who had bilateral breast cancer with those who
had unilateral disease. Women were interviewed or given a self-administered
questionnaire to ascertain whether they had been treated with tamoxifen

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after surgery for their rst breast cancer. In these mutation carriers the multivariate odds ratio for contralateral breast cancer associated with tamoxifen
use was 0.50 (95% CI, 0.280.89). Tamoxifen was associated with a lower
risk of contralateral breast cancer in BRCA1 mutation carriers (odds ratio,
0.38; 95% CI, 0.190.74) than in BRCA2 mutation carriers (odds ratio, 0.63;
95% CI, 0.201.50), even though BRCA1 mutation carriers are more likely
to develop estrogen receptornegative tumors (83% of the breast cancers developing in BRCA1 mutation carriers and 14% of those in BRCA2 mutation
carriers are estrogen receptornegative).
The dierential response rates among BRCA mutation carriers in the
NSABP P-1 trial [59] and in the case-control study of Narod and colleagues
[64] might be related to the timing of chemoprevention. Sixty percent of the
P-1 participants were 50 years old or older, whereas nearly 90% of the casecontrol participants were younger than 50 years. Given that premenopausal
oophorectomy is eective in preventing BRCA1 tumors [65], tamoxifen also
possibly should be administered before menopause.
Tamoxifen increases the risk of endometrial cancer and thromboembolism by twofold or more [66]. Raloxifene is a selective estrogen modulator
that seems to have a better safety prole (lower risk of uterine cancer and
thromboembolism) than tamoxifen [67]. A large, randomized, prospective
trial compared the impact of tamoxifen and raloxifene in lowering the
risk of breast cancer in postmenopausal women and found that the two
were equally ecacious [67]. Much less is known about the potential impact
of raloxifene in reducing breast cancer risk in BRCA mutation carriers,
however.
Thus, women who carry the BRCA mutations have three major options
to consider, with signicant trade-os. Screening is the most commonly used
option but frequently is associated with false-positive results that produce
needless anxiety. Additionally, cancers missed on screening (false-negative
results) might aect outcome adversely. Although prophylactic surgery
may reduce the risk of breast and ovarian cancer by 90%, mastectomy
may aect a womans perception of her body image, and oophorectomy prevents childbearing. Even though chemoprevention may reduce the risk of
breast cancer by as much as 50%, it increases the risk of endometrial cancer
and venous thromboembolism by more than twofold. Clinicians should
discuss the potential risks and benets of these options with BRCA mutation
carriers. Finally, the timing of intervention may be important, but this issue
is not well dened and could dier for BRCA1 and BRCA2 carriers [68].
Ultimately, the best choice is the one made by a fully informed patient.
Breast cancer treatment
If a BRCA mutation carrier develops breast cancer, options for local
therapy should be weighed carefully. Radiotherapy can be administered
safely after breast-conserving surgery in BRCA mutation carriers, although

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857

these patients are at increased risk for developing second primary cancers
(particularly contralateral breast cancers) [69]. Pierce and colleagues [70] followed 160 mutation carriers and 445 matched controls diagnosed with
breast cancer following breast-conserving surgery. Mutation carriers who
had not undergone oophorectomy had an increased risk of ipsilateral breast
tumor recurrence; those who had undergone oophorectomy did not. Many
women who have BRCA mutations opt for bilateral mastectomy, however.
A recent study of women who had BRCA1 or BRCA2 mutations who had
been diagnosed with unilateral breast cancer found that bilateral mastectomy was accepted more widely in North America than in Europe [71]. In
the United States, nearly half of all BRCA mutation carriers opted for bilateral mastectomy. At the time of mastectomy, a sentinel biopsy generally
should be performed in the axilla on the side aected by breast cancer. If
the sentinel node contains metastatic disease, a complete axillary dissection
is indicated. Patients who have signicant involvement of the axillary lymph
nodes (generally with four or more lymph nodes containing metastatic disease) should consider postmastectomy radiotherapy [72].
For BRCA mutation carriers who are diagnosed with breast cancer, the
choice of systemic therapy is determined by standard prognostic and predictive factors [69]. There are no treatments specically tailored for patients
who have BRCA mutations. Decisions concerning systemic therapy are
based both on nodal status and tumor size and, more importantly, on estrogen receptor status and HER-2 status of the tumor. Thus, BRCA mutation
carriers who are diagnosed with breast cancer should receive the same
systemic treatments as patients who have sporadic breast cancer, based on
standard prognostic and predictive factors.

Summary
Genetic testing now makes it possible to identify women who have
a greatly increased risk for developing breast cancer. Not all women who
have a family history of breast cancer are appropriate candidates for genetic
testing, however. Women must be informed about the potential risks and
benets of genetic testing, and those who are found to carry mutations in
the BRCA1 or BRCA2 genes should be advised of all management options.
Three strategies commonly are employed to manage BRCA mutation
carriers: screening, prophylactic surgery, and chemoprevention. No randomized prospective trials have addressed the impact of these interventions
in mutation carriers, however, and their potential risks and benets should
be discussed with each patient. Ultimately, many patients may elect more
than one option (eg, screening initially and then prophylactic surgery after
completing childbearing). Thus, physicians who manage patients who
have BRCA mutations should be prepared to follow these patients over
a span of many years.

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