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Open Access Highly Accessed Research article

Risk-reducing strategies for women carrying brca1/2 mutations with a focus on prophylactic surgery

Mohamed Salhab1, Selina Bismohun1 and Kefah Mokbel2*

Author Affiliations

1 St. George's University of London, London, UK

2 London Breast Institute, The Princess Grace Hospital, 45 Nottingham Place, London, W1U 5NY, UK

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BMC Women's Health 2010, 10:28  doi:10.1186/1472-6874-10-28


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1472-6874/10/28


Received:8 April 2010
Accepted:20 October 2010
Published:20 October 2010

© 2010 Salhab et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Women who have inherited mutations in the BRCA1 or BRCA2 genes have substantially elevated risks of breast and ovarian cancer. Mutation carriers have various options, including extensive and regular surveillance, chemoprevention and risk-reducing surgery. The aim of this review is to provide an up-to-date analysis and to subsequently summarise the available literature in relation to risk-reducing strategies, with a keen focus on prophylactic surgery.

Methods

The literature review is facilitated by Medline and PubMed databases. The cross-referencing of the obtained articles was used to identify other relevant studies.

Results

Prophylactic surgery (bilateral mastectomy, bilateral salpingo-oophorectomy or a combination of both procedures) has proved to be the most effective risk-reducing strategy. There are no randomised controlled trials able to demonstrate the potential benefits or harms of prophylactic surgery; therefore, the evidence has been derived from retrospective and short follow-up prospective studies, in addition to hypothetical mathematical models.

Based on the current knowledge, it is reasonable to recommend prophylactic oophorectomy for BRCA1 or BRCA2 mutation carriers when childbearing is completed in order to reduce the risk of developing breast and ovarian cancer. In addition, women should be offered the options of rigorous breast surveillance, chemoprevention with anti-oestrogens--especially for carriers of BRCA2--or bilateral prophylactic mastectomy.

Conclusion

The selection of the most appropriate risk-reducing strategy is not a straightforward task. The impact of risk-reducing strategies on cancer risk, survival, and overall quality of life are the key criteria considered for decision-making. Notably, various other factors should be taken into consideration when evaluating individual mutation carriers' individual circumstances, namely woman's age, morbidity, type of mutation, and individual preferences and expectations.

Although prospective randomised controlled trials concerned with examining the various interventions in relation to the woman's age and type of mutation are needed, randomisation is extremely difficult and rather deemed unethical given the current available evidence from retrospective studies.

Background

Breast cancer remains the leading cause of death in women aged 40-55 years[1]. Sporadic breast cancer accounts for 70-80% of all cases [2]. It is estimated that 5-10% of all breast cancers and 25%-40% of breast cancers affecting women younger than 35 years of age are attributable to hereditary causes[2]. Furthermore 60%-70% of hereditary breast cancers seem to arise secondary to germline mutations in the BRCA1 and BRCA2 genes[3,4]. Notably, ovarian cancer is a relatively rare disease: it affects one in eighty women at some point during their life time[5]. Hereditary or familial ovarian cancer is linked to many germline mutations, such as PTEN (Cowden syndrome), TP53 (Li-Fraumeni Syndrome) and ATM (ataxia-teleangiectatica-mutated gene)[6]. However, BRCA1 and BRCA2 gene mutations are found to cause the majority of autosomal-dominant inherited ovarian cancer[6].

Histologically, BRCA1-related breast cancers are predominantly of the basal subtype, with predominant lymphocytic infiltration, and are often more aggressive and associated with negative prognostic factors, as characterised by numerous mitoses, pleomorphic pattern, poor differentiation and higher proliferation rates [7-11], as well as a negative oestrogen and progesterone receptors status [8,10,12]. Moreover, a lack of HER-2 expression was observed in breast cancer tumours of BRCA1 carriers[13]. On the other hand, tumours associated with BRCA2 mutations are of a luminal subtype, and tend to be of a positive oestrogen and progesterone receptors-status; negative HER-2, on the other hand, do not markedly differ from other hereditary or sporadic breast cancers[14]. DCIS is found to be equally as prevalent in patients who carry deleterious BRCA mutations as in high familial-risk women who are non-carriers, but ultimately occurs at an earlier age. Interestingly, BRCA mutations were found in a significant portion of women with DCIS who were presented for a hereditary risk assessment[15]. Notably, high-grade DCIS is also more common in BRCA1 mutation carriers than in those patients without any mutation[16]. Accordingly, it has been suggested that BRCA1/2-associated breast cancers progress through the same intermediate steps as sporadic breast cancers, and that DCIS should be considered as a part of the BRCA1/2 tumour spectrum[17].

Clinically, breast cancer is believed to begin at an earlier age in BRCA1 and BRCA2 gene mutation carriers compared with sporadic cases. The median age of breast cancer onset ranges from 40-50 years in BRCA1 and BRCA2 carriers compared with 60-70 years in sporadic cases[18,19]. Furthermore, breast tumours in BRCA1/2 carriers are more likely to be bilateral and affect the contra lateral breast at a later stage [8,12,19]. Furthermore, BRCA1/2 mutation carriers also have a higher rate of pregnancy-associated breast cancer before the age of 50[20,21].

Several studies have suggested no significant differences between BRCA-associated breast cancer and non-BRCA associated breast cancer in relapse-free, event-free, and overall survival [22-24]. On the other hand, other studies indicate that BRCA-associated breast cancer presents worse survival rates and overall prognosis [14,25-28]. Inconsistencies in previous studies may be due to limitations in study design: in particular, the studies contain small numbers of BRCA cases. Additionally, due to the onset occurring at an extremely early age of those patients with BRCA mutations, it was not always possible to obtain controls which were considered adequately matched for age. In addition, inconsistencies in previous studies were due to the examination of both BRCA1 and BRCA2 mutation groups together. Lee et al., for example, recently conducted a meta-analysis of 11 previously published articles [29]. The analysis shows that the BRCA1 mutation carriers have worse predicted overall survival rates (approximately 5 years) than non-carriers (HR = 1.94, 95% CI, 1.45-2.53). Furthermore, long-term overall survival (10 years or greater) was found to be worse in BRCA1 mutation carriers compared with non-carriers (HR = 1.33, 95% CI, 1.12-1.58). However, they indicate that there has been no significant heterogeneity observed across the studies.

Moreover, Lee et al. observes that short-term progression-free survival in BRCA1 carriers was worse than in non-BRCA carriers (HR = 1.54). Such observations were not witnessed in long-term progression survival. In addition, BRCA2 mutation was not observed to affect either short- or long-term survival rates, which may be attributed to the different carcinogenic pathways for BRCA1 and BRCA2 [29].

Most ovarian cancers associated with germ line BRCA mutations are diagnosed at a younger age and are ultimately determined as high-grade and advanced-stage serous carcinomas[30]. They have surgical and pathological characteristics similar to those of sporadic cancers. BRCA mutations do not seem to play a significant role in the development of mucinous or borderline ovarian tumours[21]. Moreover, BRCA1 germline mutation carriers are not only at risk of ovarian cancer, but also fallopian tube carcinoma and peritoneal papillary serous carcinoma[31]. Olivier et al. suggest that peritoneal papillary serous carcinoma risk amongst BRCA2 carriers is lower than amongst BRCA1 carriers[31]. Furthermore, hereditary ovarian cancer has a distinctly better clinical outcome with a longer overall survival and recurrence-free interval after chemotherapy than sporadic cancers[21]. Notably, it has been observed that BRCA-positive Epithelial Ovarian Cancer patients have better outcomes than non-hereditary epithelial ovarian cancer patients [32], and advanced-stage hereditary cancer patients survive longer than nonhereditary cancer patients[33].

The identification of BRCA1 and BRCA2 genes in 1994 and 1995 respectively[34,35] has had a great impact on the understanding and management of sporadic and hereditary breast and ovarian cancers. Whilst the risk of breast and ovarian cancer in the general population is 10%-13% and 1.7%, respectively, studies indicate that a woman with mutations in either BRCA1 or BRCA2 carries a lifetime breast cancer risk of 80% and 20%-60% for developing breast cancer and ovarian cancer respectively[3,36]. In the case of BRCA1 gene mutation carriers, the cumulative risk of cancer by the age of 70 years ranges between 51% and 95% for breast cancer, and between 22% and 60% for ovarian cancer. Similar trends are also observed in BRCA2 carriers, as the risk ranges between 33% and 95% for breast cancer, and between 4% and 47% for ovarian cancer[37].

Women who have an increased risk of breast and ovarian cancer are advised to consider risk-reducing strategies; however, such methods vary in their effectiveness. These strategies include surveillance (breast self-examination, clinical breast examination, screening using mammography and breast magnetic resonance imaging (MRI), trans-vaginal ultrasound scanning and serum (CA125), chemoprevention and prophylactic surgery (salpingo-oophorectomy and/or mastectomy)[38,39]. Risk-reducing strategies have been shown to have associations with a gain in life expectancy in BRCA1/2 carriers. Moreover, extended life expectancy can range from between a few months to a few years, although this is ultimately dependent on the prophylactic intervention (Table 1).

Table 1. Life expectancy gains from cancer prevention strategies for BRCA1/2 positive women

The aim of this review is to provide an up-to-date analysis and to subsequently summarise the available literature in relation to risk-reducing strategies, with a keen focus on prophylactic surgery.

Methods

MEDLINE and PubMed were used to search for relative articles. Articles identified using the key words "breast cancer", "BRCA1", "BRCA2", "ovarian cancer", "risk reducing", "prophylactic", "mastectomy", "oophorectomy" and "life expectancy". Cross referencing was performed to identify other articles not identified at the initial search.

Results

Surveillance

The efficacy of surveillance in BRCA1/2 mutation carriers is difficult to determine. Importantly, it has been suggested that some BRCA1/2 carriers will not develop cancer during their lifetime[40], although the identification of such individuals is currently impossible. The concept of surveillance is based on early detection of cancer rather than cancer prevention. It is suggested that women at a high risk of developing breast cancer should perform a monthly breast self-examination, and also undergo bi-annual clinical examination[41,42] and annual digital mammography. Owing to the fact that the sensitivity of mammography is significantly reduced in younger women because of their dense breast tissue and rapid development of breast cancer in BRCA1/2 mutations, the use of alternative and more sensitive imaging modalities, such as MRI at shorter intervals, has been recommended[42-44]. However, the malignant lesions in BRCA mutation carriers frequently have morphological characteristics which are commonly seen in benign lesions, such as a rounded shape or sharp margins. With this in mind, MRI has the ability to evaluate the enhancement pattern and kinetics, and hence enables the detection of characteristics suggestive of a malignancy[45]. The use of MRI in addition to digital mammography for surveillance in BRCA mutation carriers is considered to be essential in such women--even if their breast density is low[46]. Undoubtedly, surveillance is the least invasive option; however, such a method is associated with various negative consequences, such as increased anxiety, false reassurance, and unnecessary biopsies[47,48]. Although MRI is an effective surveillance modality in BRCA mutation carriers--especially in younger women--a significant proportion of women are still found to have node positive breast cancer at the time of diagnosis[49]. Furthermore, whilst regular surveillance in women at an increased familial risk of breast cancer is associated with a good clinical outcome if they carry BRCA2 mutations or no detectable mutation, the outcome in carriers of BRCA1 mutations is significantly worse, even in the instance that their tumours are diagnosed at an apparently early stage[27]. The impact of regular breast screening in this context on overall survival ultimately remains unclear, and further research is required in order to evaluate the effect of different breast-screening strategies according to the mutation type, type and frequency of screening modality, and age.

Importantly, annual ovarian surveillance--conducted by pelvic examination, trans-vaginal ultrasound scanning and serum CA125 measurement--in women at increased familial risk of ovarian cancer is found to be ineffective in detecting tumours at a sufficiently early stage, which substantially influences survival in BRCA1/2 mutation carriers[50-52]. Serum proteomics technology is currently being evaluated in the context of ovarian cancer detection and seems to be promising.

Chemoprevention

It is well recognised that oestrogen plays an essential role in mammary carcinogenesis by exerting a carcinogenic effect (through metabolites) on cellular DNA and thereby promoting the growth of ER positive breast cancer[53]. Therefore, chemo-prevention strategies aim to target the oestrogen receptor signalling pathway or oestrogen synthesis. Selective oestrogen receptor modulators (SERMs) have been suggested as chemo-preventative agents in BRCA mutation carriers. In a subgroup analysis of the National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) trial [54], Tamoxifen was found to reduce the incidence of breast cancer in healthy BRCA2 mutation carriers but not in BRCA1 carriers when started at the age 35 years or older[55]. These findings are not surprising given the fact that BRCA2-related breast cancers are largely ER-positive tumours, whilst BRCA1-related breast cancers are predominantly ER-negative[14,56,57]. Furthermore, in BRCA1 or BRCA2 carriers with breast cancer, Tamoxifen use was associated with the prevention of secondary and contra lateral breast cancer[58,59].

Prophylaxis with SERMs was estimated to prolong survival by 1.6 to 2.2 years in BRCA gene mutation carriers[60]. The ablation of the endometrial lining can be considered in BRCA mutation carriers who opt for chemoprevention with Tamoxifen in order to reduce the risk of endometrial tumours.

Targeting oestrogen synthesis is considered to be an alternative to SERMs as a chemo-preventative risk-reducing strategy in high-risk women. Aromatase inhibitors (AIs) have been shown to be superior to Tamoxifen in the treatment of ER-positive breast cancer and the prevention of contralateral breast cancer in postmenopausal women with fewer side effects. It is likely that AIs will have a prophylactic role to play in BRCA gene carriers who opt to have prophylactic oophorectomy (PO) and breast surveillance. However, this potential role requires further evaluation through prospective controlled trials, with the inclusion of quality of life issues and skeletal complications as secondary endpoints.

Based on the knowledge that the risk of ovarian cancer and mortality is reduced by 50% and 80% respectively in long-term users of oral contraceptive pills (OCPs)[61,62], OCPs are considered as potential preventative measures for women at high risk of developing ovarian cancer. The use of OCPs was associated with significant ovarian cancer risk reduction in a case control study when used for a period of 6 or more years by BRCA1/2 carriers[63]. However further research is required in order to assess the chemo-preventative role of OCP amongst high-risk subjects. Furthermore, their use is known to be associated with an increased risk of breast cancer[64]; hence, their use should be considered in carefully selected candidates.

The non-specific action of existing DNA damage reagents poses a problem regarding chemoprevention in BRCA women. Such agents have been found to cause a similar extent of damage in both BRCA1 mutant and wild-type cells. The recent discovery that PARP-1 inhibitors kill BRCA1/2 deficient cells with a high level of specificity subsequently opens up a potential therapy which looks very hopeful for BRCA1 cancer patients. A number of studies have illustrated that BRCA1/2 pre-cancerous cells are very sensitive to PARP inhibition, whilst cancer cells exhibit different responses to PARP inhibition under a variety of different conditions. Furthermore, it has been suggested that these differences in PARP sensitivity can be attributed to distinct phases in BRCA associated tumorigenesis. Work conducted by De Soto & Deng[65] demonstrates that, during the early stages of tumorigenesis, there is a clear sensitivity of BRCA mutant cells to PARP inhibition. This has led to the inference that BRCA-deficient cells in this early pre-cancerous state receive a permissive mutation which is sensitive to PARP-1 inhibitors. Such agents may prove effective in reducing breast cancer risk amongst BRCA1 and 2 carriers.

Prophylactic Surgery

Risk-reducing surgery in BRCA1/2 gene mutation carriers includes prophylactic bilateral salpingo-oophorectomy (PBSO) and/or prophylactic bilateral mastectomy (PBM). The aim of surgery is to reduce the risk of cancer development and to reduce mortality.

Notably, extensive counselling should be offered to all women who consider prophylactic surgery, including a detailed explanation of the cancer risk, complications associated with surgery, aesthetic outcome, quality of life issues, and potential life expectancy gain. The decision to proceed with prophylactic surgery is largely patient-driven depending on whether the patient feels comfortable living with the estimated risk and how she values the psychosexual function of the breast and ovaries. It is observed that many women who undergo BRCA testing use these results to make clinical decisions; those who choose risk-reducing surgeries typically do so within months of receiving BRCA-positive results. Predictors of risk-reducing surgery uptake include age below 60 years, prior breast cancer, and utilisation of another risk-reducing surgery.

Since the establishment of the link between breast and ovarian cancers and BRCA1/2 genes mutations, in addition to the increasing availability of genetic testing, research groups were faced with many questions concerning the efficacy and usefulness of risk-reducing surgery. Earlier studies have more keenly focused on decisions concerning whether or when to undergo prophylactic surgery. The magnitude of the potential benefit fundamentally depends on the risk of cancer associated with specific mutations, the prognosis of the tumours in carriers of the mutations, and the extent to which relief of anxiety could result from surgical prophylaxis. These benefits were to be weighed against an array of potential costs, including surgical complications and the potential impacts of mastectomy or oophorectomy on a woman's self-image, as well as on their sexual and reproductive function[66].

Prophylactic bilateral mastectomy (PBM)

There are no randomised controlled trials which have previously examined the potential impacts of PBM on survival; therefore, evidence has been derived from retrospective and short follow-up prospective studies in addition to hypothetical mathematical models with variable estimates.

Earlier studies have utilised the Markov model[60], which was developed with the objective to determine the survival benefits in BRCA1/2 carriers who undergo different types of prophylactic surgery. In studies performed by Grann et al., it was concluded that a 30-year-old BRCA1/2 positive woman could prolong her survival by 0.9 years (95% probability interval, 0.4-1.2 years) by having bilateral oophorectomy, 3.4 years (2.7-3.7 years) by having bilateral mastectomy, and 4.3 years (3.6-4.6 years) by having both procedures compared with surveillance alone. Chemoprevention with Tamoxifen and raloxifene was estimated to increase survival by 1.6 years (1.0-2.1 years) and 2.2 years (1.3-2.8 years), respectively. These findings suggest that prophylactic surgery is associated with substantial survival benefits[67,68]. Other authors show that, compared with breast and ovarian screening, the average gain in life expectancy for 30-year-old carriers in the high- and medium-risk categories was 11.7 and 6.6 years respectively for combined prophylactic mastectomy and oophorectomy, 9.5 and 5.3 years respectively for breast-screening and prophylactic oophorectomy, and 4.9 and 4.4 years respectively for prophylactic mastectomy with ovarian screening. This indicates that combined prophylactic mastectomy and oophorectomy is the most effective strategy for prolonging life[69]. Furthermore, PO seems to be superior to BPM in terms of prolonging survival. Similar findings were reported by Schrag et al. [70]; however, the authors suggest that gains in life expectancy decline with age at the time of prophylactic surgery, and are minimal for 60-year-old women. Also, amongst 30-year-old women, oophorectomy may be delayed by 10 years with little loss of life expectancy.

Furthermore, in the case of carriers of BRCA1/2 mutations who subsequently developed breast cancer, it was found that, with the use of the Markov model and depending on the assumed penetrance of the BRCA mutation, probabilities associated with developing contra lateral breast cancer and ovarian cancer, dying from these cancers, dying from primary breast cancer, and the reduction in cancer incidence and mortality due to prophylactic surgeries and compared with surveillance alone, 30-year-old early-stage breast cancer patients with BRCA mutations showed a gain in life expectancy of approximately 0.4 to 1.3 years from Tamoxifen therapy, 0.2 to 1.8 years from PO, and 0.6 to 2.1 years from prophylactic contralateral mastectomy (PCM). The magnitude of these gains is believed to be least for those women with low-penetrance mutations (assumed contra lateral breast cancer risk of 24% and ovarian cancer risk of 6%) and greatest for those with high-penetrance mutations (assumed contra lateral breast cancer risk of 65% and ovarian cancer risk of 40%). Notably, older age and poorer prognosis from primary breast cancer further attenuate such gains [71]. Undoubtedly, estimates of life expectancy gain may help women and their physicians consider the uncertainties, risks, and advantages of such interventions, and may accordingly lead to more informed choices concerning cancer prevention strategies[71].

In recent years, a few cohort and case control studies have considered the effectiveness of prophylactic surgery. However, it is of great importance to mention that they differ in quality, with some having significant methodological flaws--mainly owing to selection bias and retrospective study design.

Prophylactic bilateral mastectomy reduces the risk of breast cancer in BRCA mutation carriers by 85%-100%[72-74]. In a report published by Rebbeck et al., 483 women with BRCA1/2 mutations were studied. After a mean follow-up of 6.4 years, breast cancer was diagnosed in two (1.9%) of 105 women who had bilateral prophylactic mastectomy, and in 184 (48.7%) of 378 matched controls who did not have the procedure. The group therefore subsequently concludes that BPM reduces the risk of breast cancer in women with BRCA1/2 mutations by approximately 90%[74]. Furthermore, in a prospective study of 139 women with BRCA1 or BRCA2 mutations, after a mean follow-up of 3 years, breast cancer developed in 8 of 63 women who had elected surveillance, but in none of the 76 BRCA mutations carriers who had undergone prophylactic surgery[73]. Similarly, a report on an extended series with a longer follow-up of women with BRCA1/2 mutation having undergone PBM at the Rotterdam Family Cancer Clinic found that no primary breast cancer occurred after PBM after a median follow-up of 4.5 years, with one woman presenting metastatic breast cancer almost four years after her PBM where no primary was found[75].

It is accepted that no surgical technique for prophylactic mastectomy removes all breast epithelium; simple mastectomy removes approximately 95%-99% of breast glandular tissue; however, it causes a significant deformity, changes in body image and sexuality, as well as adverse effects on the psychosocial status of the affected woman, but not quality of life[76]. Moreover, it has been observed that most women opting for prophylactic mastectomy experienced significantly higher distress levels than mutation carriers who opted for surveillance as well as non-mutation carriers. This difference in levels of distress was found to be highest during pre- and post-test stages, and had almost disappeared during the one-year follow-up. Moreover, mutation carriers opting for prophylactic mastectomy are more often in their thirties, more often have young children, and also have a greater awareness of the genetic nature of cancer in the family than those opting for regular surveillance. Interestingly, their distress levels seem to significantly decrease 6 months or longer following surgery, possibly due to the significant risk reduction of developing breast cancer[77]. Furthermore, those undergoing mastectomy with delayed reconstruction report a lower impact on their self-esteem and sexual life versus those who only had the mastectomy[78].

Skin sparing mastectomy and immediate breast reconstruction (SSM & IMR) has been proved to be oncologically safe, and is associated with high satisfaction rate and low morbidity[79,80]. More recently, there has been increasing interest in offering BRCA1/2 carriers SSM and IBR, either by using an autologous flap, implant or both. On the other hand, SSM and IBR have many aesthetic advantages[81], and so it is fundamental to recognise that 5%-10% of breast tissue can be left in the subcutaneous flaps. This residual breast tissue may be a focus for breast cancer development in high-risk women with BRCA mutations; therefore, SSM or nipple-sparing mastectomy in risk-reducing surgery setting is feasible in most patients at an increased risk; however, it should be the subject of further prospective evaluations in order to ascertain its long-term oncological safety[82].

Prophylactic bilateral salpingo-oophorectomy (PBSO)

Since breast tumours are largely oestrogen-driven, it has been suggested that the hormonal blockade by oophorectomy inhibits the development of breast tumours[83]. Importantly, prophylactic oophorectomy has the advantage of preventing ovarian cancer as well as breast cancer. Prophylactic salpingo-oophorectomy, and the sectioning of both tubes and ovaries, is recommended in order to ensure occult carcinomas are not missed. Furthermore, since BRCA mutation carriers develop fallopian tube carcinoma and peritoneal papillary serous carcinoma, PBSO and sectioning both tubes and ovaries is therefore recommended in order to ensure occult carcinomas are not missed[31]. The demonstrated efficacy of oophorectomy in the case of BRCA mutation carriers is interesting, simply because most BRCA1-related breast tumours are negative for oestrogen receptors[9-11]. This observation can be attributed to the carcinogenic effect of oestrogen metabolites-DNA adducts[84].

In a large, retrospective analysis of 551 BRCA carriers, BSO was found to have reduced the risk of ovarian cancer by 96% and breast cancer by 53% at a mean follow-up of 9 years[85]. Similar findings were observed in a prospective study of 170 BRCA carriers. During a mean follow-up of 2 years, the incidence of ovarian or peritoneal cancer and breast cancer was significantly greater amongst those women who selected surveillance than amongst those who chose to undergo PBSO[86]. In a multicentre prospective study, Kauff et al. found that, during a 3-year follow-up, BPSO was associated with 85% reduction in BRCA1-associated gynaecologic cancer risk and 72% reduction in BRCA2-associated breast cancer risk. Although protection against BRCA1-associated breast cancer and BRCA2-associated gynaecologic cancer was suggested, neither effect reached statistical significance. The authors postulate that the protection conferred by PBSO against breast and gynaecologic cancers may differ between the carriers of BRCA1 and BRCA2 mutations[87].

Although several studies demonstrate that PBSO decreased the risk of both breast and ovarian cancers in BRCA1/2 mutation carriers[85-94], these studies were nevertheless heterogeneous and used different designs: whilst some were retrospective case control studies, others used a prospective cohort design. Even amongst prospective studies, the inclusion criteria and the definitions of follow-up times differed. In some studies, only unaffected mutation-positive women were included and followed up; whilst in others--particularly when examining ovarian cancer risk--women with breast cancer were included. Such differences in study design can introduce biases (such as survival bias), and can consequently have an impact on risk-reduction estimates.

Recently, Rebbeck et al. carried out a meta-analysis of ten studies which investigated breast or gynaecologic cancer outcomes in BRCA1/2 mutation carriers who had undergone PBSO. The authors subsequently concluded that PBSO was associated with a statistically significant reduction in breast cancer risk amongst BRCA1/2 mutation carriers. Similar risk reductions were observed in BRCA1 mutation carriers and in BRCA2 mutation carriers. Furthermore, PBSO was associated with a statistically significant reduction in the risk of BRCA1/2-associated ovarian or fallopian tube cancer; however, data were deemed insufficient to obtain separate estimates for ovarian or fallopian tube cancer risk reduction. Moreover, PBSO was strongly associated with reductions in the risk of breast, ovarian, and fallopian tube cancers, and should provide guidance to women in planning cancer risk-reduction strategies[95].

Furthermore, in a prospective study with a short-term follow-up, PBSO was associated with a 90% reduction in breast cancer-specific mortality, a 95% reduction in gynaecologic cancer-specific mortality, and a 76% reduction in overall mortality [89]. Such data demonstrate the utility of BSO in this population of patients given the fact that the procedure can be performed laparoscopically with minimal invasiveness, high efficacy, and low morbidity[96]. Chemoprevention with anti-oestrogens--especially in BRCA2 carriers--and breast surveillance can be added to PBSO in order to enhance its effective prophylactic role with a limited impact on quality of life.

Limitations

This review paper provides an up-to-date analysis of our understanding of the advantages of risk-reducing strategies in BRCA carriers. Although the article summarises the evidence which suggests that different strategies are associated with varying degrees of cancer risk-reduction, such evidence is nevertheless derived from retrospective and short follow-up prospective studies in addition to hypothetical mathematical models. It is known that retrospective studies do not provide the highest level of evidence compared with randomised controlled studies; they are often less robust and usually carry a degree of bias. Furthermore, they tend not to be standardised in relation to confounding factors, such as patients' age, socio-economic class, and other factors.

Currently, there are no randomised controlled trials concerned with the demonstration of the potential benefits or harms of prophylactic surgery. This is due to different factors, such as the small number of BRCA mutation carriers, which necessitate multiple centres to participate. Conducting a randomised controlled trial in multiple centres poses potential problems, namely a lack of standardisation, which is the main issue as different surgeons have different surgical risk-reducing techniques. Furthermore, in light of the currently available evidence from retrospective studies, randomisation is deemed unethical, and women may therefore opt for risk-reducing surgery rather than observation.

Conclusions

Selecting the most appropriate risk-reducing strategy is not a straightforward task. The impact of risk-reducing strategies on cancer risk, survival, and overall quality of life are the key criteria considered for making a good decision. There is no sole risk-reducing strategy which is able to fully meet all expectations and requirements in an individual woman. On the one hand, non-surgical procedures provide a good body image and quality of life, but may be associated with increased risk of advanced-stage cancer and mortality; on the other hand, surgery ensures a very high protection from cancer but is associated with a number of disadvantages of invasiveness, non-reversibility and surgical morbidity.

Based on the available literature, it is deemed appropriate to acknowledge that the clinical management of cancer risk in BRCA1 and BRCA2 mutation carriers is a rather complex and stressful task, which should consider individual patients' expectations and preferences. Such preferences can be informed by accurate knowledge of the risks and benefits of the interventions considered. Available studies confirm the essential role of PBSO in reducing the risk of both breast and ovarian cancer. Furthermore, other options for risk reduction should be considered, such as chemoprevention and risk-reducing mastectomy[74]. Although coordinated, PBM and PBSO are feasible procedures with acceptable morbidity in selected high-risk patients[97]; the timing of prophylactic surgery is still a matter of paramount importance to both patients and clinicians to consider during the counselling process.

It is recommended that prophylactic surgery should be performed as soon as possible, simply because of the early development of cancer in BRCA mutation carriers. Although ovarian cancer rarely occurs in premenopausal women, it is advised that BRCA mutation carriers should undergo PBSO immediately after childbearing is complete in order to reduce the risk of early breast cancer development.

Prospective randomised controlled trials examining the various interventions in relation to the woman's age and type of mutation are needed. However, the randomisation of BRCA carriers to different arms of trials is an extremely difficult and rather impossible process given the current available evidence.

Abbreviations

DCIS: Ductal carcinoma in-situ; MRI: Magnetic resonance imaging; SERMs: Selective oestrogen receptor modulators; AIs: Aromatase inhibitors; PO: Prophylactic oophorectomy; OCPs: Oral contraceptive pills; PBSO: Prophylactic bilateral salpingo-oophorectomy; PBM: Prophylactic bilateral mastectomy; PCM: Prophylactic contralateral mastectomy; SSM: Skin sparing mastectomy; IBR: Immediate breast reconstruction

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MS performed literature search/review and manuscript writing. SB: helped in manuscript writing, KM involved in the concept, manuscript revision and writing. All authors read and approved the final manuscript.

Acknowledgements

We are grateful to Breast Cancer Hope Charity (Reg: 1110926) for funding and supporting the production of this article.

References

  1. Bailar JC III, Gornik HL: Cancer undefeated.

    N Engl J Med 1997, 336:1569-1574. PubMed Abstract | Publisher Full Text OpenURL

  2. Goldberg JI, Borgen PI: Breast cancer susceptibility testing: past, present and future.

    Expert Rev Anticancer Ther 2006, 6:1205-1214. PubMed Abstract | Publisher Full Text OpenURL

  3. Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, et al.: Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.

    Am J Hum Genet 2003, 72:1117-1130. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  4. Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, et al.: Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.

    Am J Hum Genet 1998, 62:676-689. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  5. Bray F, Loos AH, Tognazzo S, La Vecchia C: Ovarian cancer in Europe: Cross-sectional trends in incidence and mortality in 28 countries, 1953-2000.

    Int J Cancer 2005, 113:977-990. PubMed Abstract | Publisher Full Text OpenURL

  6. Fearon ER: Human cancer syndromes: clues to the origin and nature of cancer.

    Science 1997, 278:1043-1050. PubMed Abstract | Publisher Full Text OpenURL

  7. Eisinger F, Jacquemier J, Charpin C, Stoppa-Lyonnet D, Bressac-de Paillerets B, Peyrat JP, et al.: Mutations at BRCA1: the medullary breast carcinoma revisited.

    Cancer Res 1998, 58:1588-1592. PubMed Abstract | Publisher Full Text OpenURL

  8. Johannsson OT, Idvall I, Anderson C, Borg A, Barkardottir RB, Egilsson V, et al.: Tumour biological features of BRCA1-induced breast and ovarian cancer.

    Eur J Cancer 1997, 33:362-371. PubMed Abstract | Publisher Full Text OpenURL

  9. Lakhani SR, Jacquemier J, Sloane JP, Gusterson BA, Anderson TJ, van de Vijver MJ, et al.: Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations.

    J Natl Cancer Inst 1998, 90:1138-1145. PubMed Abstract | Publisher Full Text OpenURL

  10. Robson M, Gilewski T, Haas B, Levin D, Borgen P, Rajan P, et al.: BRCA-associated breast cancer in young women.

    J Clin Oncol 1998, 16:1642-1649. PubMed Abstract | Publisher Full Text OpenURL

  11. Veronesi A, de Giacomi C, Magri MD, Lombardi D, Zanetti M, Scuderi C, et al.: Familial breast cancer: characteristics and outcome of BRCA 1-2 positive and negative cases.

    BMC Cancer 2005, 5:70. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

  12. Ansquer Y, Gautier C, Fourquet A, Asselain B, Stoppa-Lyonnet D: Survival in early-onset BRCA1 breast-cancer patients. Institut Curie Breast Cancer Group.

    Lancet 1998, 352:541. PubMed Abstract | Publisher Full Text OpenURL

  13. Petersson C, Pandis N, Mertens F, Adeyinka A, Ingvar C, Ringberg A, et al.: Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families.

    Genes Chromosomes Cancer 1996, 16:185-188. PubMed Abstract | Publisher Full Text OpenURL

  14. Brekelmans CT, Tilanus-Linthorst MM, Seynaeve C, vd OA, Menke-Pluymers MB, Bartels CC, et al.: Tumour characteristics, survival and prognostic factors of hereditary breast cancer from BRCA2-, B.

    Eur J Cancer 2007, 43:867-876. PubMed Abstract | Publisher Full Text OpenURL

  15. Smith KL, Adank M, Kauff N, Lafaro K, Boyd J, Lee JB, et al.: BRCA mutations in women with ductal carcinoma in situ.

    Clin Cancer Res 2007, 13:4306-4310. PubMed Abstract | Publisher Full Text OpenURL

  16. Hwang ES, McLennan JL, Moore DH, Crawford BB, Esserman LJ, Ziegler JL: Ductal carcinoma in situ in BRCA mutation carriers.

    J Clin Oncol 2007, 25:642-647. PubMed Abstract | Publisher Full Text OpenURL

  17. Arun B, Vogel KJ, Lopez A, Hernandez M, Atchley D, Broglio KR, et al.: High prevalence of preinvasive lesions adjacent to BRCA1/2-associated breast cancers.

    Cancer Prev Res (Phila Pa) 2009, 2:122-127. OpenURL

  18. Gaffney DK, Brohet RM, Lewis CM, Holden JA, Buys SS, Neuhausen SL, et al.: Response to radiation therapy and prognosis in breast cancer patients with BRCA1 and BRCA2 mutations.

    Radiother Oncol 1998, 47:129-136. PubMed Abstract | Publisher Full Text OpenURL

  19. Verhoog LC, Brekelmans CT, Seynaeve C, van den Bosch LM, Dahmen G, van Geel AN, et al.: Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1.

    Lancet 1998, 351:316-321. PubMed Abstract | Publisher Full Text OpenURL

  20. Cullinane CA, Lubinski J, Neuhausen SL, Ghadirian P, Lynch HT, Isaacs C, et al.: Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers.

    Int J Cancer 2005, 117:988-991. PubMed Abstract | Publisher Full Text OpenURL

  21. Jernstrom H, Lerman C, Ghadirian P, Lynch HT, Weber B, Garber J, et al.: Pregnancy and risk of early breast cancer in carriers of BRCA1 and BRCA2.

    Lancet 1999, 354:1846-1850. PubMed Abstract | Publisher Full Text OpenURL

  22. Brekelmans CT, Seynaeve C, Menke-Pluymers M, Bruggenwirth HT, Tilanus-Linthorst MM, Bartels CC, et al.: Survival and prognostic factors in BRCA1-associated breast cancer.

    Ann Oncol 2006, 17:391-400. PubMed Abstract | Publisher Full Text OpenURL

  23. El Tamer M, Russo D, Troxel A, Bernardino LP, Mazziotta R, Estabrook A, et al.: Survival and recurrence after breast cancer in BRCA1/2 mutation carriers.

    Ann Surg Oncol 2004, 11:157-164. PubMed Abstract | Publisher Full Text OpenURL

  24. Musolino A, Bella MA, Bortesi B, Michiara M, Naldi N, Zanelli P, et al.: BRCA mutations, molecular markers, and clinical variables in early-onset breast cancer: a population-based study.

    Breast 2007, 16:280-292. PubMed Abstract | Publisher Full Text OpenURL

  25. Stoppa-Lyonnet D, Ansquer Y, Dreyfus H, Gautier C, Gauthier-Villars M, Bourstyn E, et al.: Familial invasive breast cancers: worse outcome related to BRCA1 mutations.

    J Clin Oncol 2000, 18:4053-4059. PubMed Abstract | Publisher Full Text OpenURL

  26. Moller P, Borg A, Evans DG, Haites N, Reis MM, Vasen H, et al.: Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy.

    Int J Cancer 2002, 101:555-559. PubMed Abstract | Publisher Full Text OpenURL

  27. Moller P, Evans DG, Reis MM, Gregory H, Anderson E, Maehle L, et al.: Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation status.

    Int J Cancer 2007, 121:1017-1020. PubMed Abstract | Publisher Full Text OpenURL

  28. Foulkes WD, Chappuis PO, Wong N, Brunet JS, Vesprini D, Rozen F, et al.: Primary node negative breast cancer in BRCA1 mutation carriers has a poor outcome.

    Ann Oncol 2000, 11:307-313. PubMed Abstract | Publisher Full Text OpenURL

  29. Lee EH, Park SK, Park B, Kim SW, Lee MH, Ahn SH, et al.: Effect of BRCA1/2 mutation on short-term and long-term breast cancer survival: a systematic review and meta-analysis.

    Breast Cancer Res Treat 2010, 122:11-25. PubMed Abstract | Publisher Full Text OpenURL

  30. Prat J, Ribe A, Gallardo A: Hereditary ovarian cancer.

    Hum Pathol 2005, 36:861-870. PubMed Abstract | Publisher Full Text OpenURL

  31. Olivier RI, van Beurden M, Lubsen MA, Rookus MA, Mooij TM, van de Vijver MJ, et al.: Clinical outcome of prophylactic oophorectomy in BRCA1/BRCA2 mutation carriers and events during follow-up.

    Br J Cancer 2004, 90:1492-1497. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  32. Tan DS, Rothermundt C, Thomas K, Bancroft E, Eeles R, Shanley S, et al.: "BRCAness" syndrome in ovarian cancer: a case-control study describing the clinical features and outcome of patients with epithelial ovarian cancer associated with BRCA1 and BRCA2 mutations.

    J Clin Oncol 2008, 26:5530-5536. PubMed Abstract | Publisher Full Text OpenURL

  33. Boyd J, Sonoda Y, Federici MG, Bogomolniy F, Rhei E, Maresco DL, et al.: Clinicopathologic features of BRCA-linked and sporadic ovarian cancer.

    JAMA 2000, 283:2260-2265. PubMed Abstract | Publisher Full Text OpenURL

  34. Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, et al.: A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.

    Science 1994, 266:66-71. PubMed Abstract | Publisher Full Text OpenURL

  35. Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, et al.: Identification of the breast cancer susceptibility gene BRCA2.

    Nature 1995, 378:789-792. PubMed Abstract | Publisher Full Text OpenURL

  36. Nelson HD, Huffman LH, Fu R, Harris EL: Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force.

    Ann Intern Med 2005, 143:362-379. PubMed Abstract OpenURL

  37. Tranchemontagne BLBIJ: Contribution of BRCA1/2 mutation testing to risk assessment for susceptibility to breast and ovarian cancer.

    Summary report Montreal: Agence d'Evaluation des Technologies et des Modes d'Intervention en Sante (AETMIS) 2006, 259. OpenURL

  38. Fatouros M, Baltoyiannis G, Roukos DH: The predominant role of surgery in the prevention and new trends in the surgical treatment of women with BRCA1/2 mutations.

    Ann Surg Oncol 2008, 15:21-33. PubMed Abstract | Publisher Full Text OpenURL

  39. Jatoi I, Anderson WF: Management of women who have a genetic predisposition for breast cancer.

    Surg Clin North Am 2008, 88:845-viii. PubMed Abstract | Publisher Full Text OpenURL

  40. Brose MS, Rebbeck TR, Calzone KA, Stopfer JE, Nathanson KL, Weber BL: Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program.

    J Natl Cancer Inst 2002, 94:1365-1372. PubMed Abstract | Publisher Full Text OpenURL

  41. Pichert G, Bolliger B, Buser K, Pagani O: Evidence-based management options for women at increased breast/ovarian cancer risk.

    Ann Oncol 2003, 14:9-19. PubMed Abstract | Publisher Full Text OpenURL

  42. Smith RA, Saslow D, Sawyer KA, Burke W, Costanza ME, Evans WP III, et al.: American Cancer Society guidelines for breast cancer screening: update 2003.

    CA Cancer J Clin 2003, 53:141-169. PubMed Abstract | Publisher Full Text OpenURL

  43. Granader EJ, Dwamena B, Carlos RC: MRI and mammography surveillance of women at increased risk for breast cancer: recommendations using an evidence-based approach.

    Acad Radiol 2008, 15:1590-1595. PubMed Abstract | Publisher Full Text OpenURL

  44. Komenaka IK, Ditkoff BA, Joseph KA, Russo D, Gorroochurn P, Ward M, et al.: The development of interval breast malignancies in patients with BRCA mutations.

    Cancer 2004, 100:2079-2083. PubMed Abstract | Publisher Full Text OpenURL

  45. Veltman J, Mann R, Kok T, Obdeijn IM, Hoogerbrugge N, Blickman JG, et al.: Breast tumor characteristics of BRCA1 and BRCA2 gene mutation carriers on MRI.

    Eur Radiol 2008, 18:931-938. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  46. Bigenwald RZ, Warner E, Gunasekara A, Hill KA, Causer PA, Messner SJ, et al.: Is mammography adequate for screening women with inherited BRCA mutations and low breast density?

    Cancer Epidemiol Biomarkers Prev 2008, 17:706-711. PubMed Abstract | Publisher Full Text OpenURL

  47. Rijnsburger AJ, Essink-Bot ML, van Dooren S, Borsboom GJ, Seynaeve C, Bartels CC, et al.: Impact of screening for breast cancer in high-risk women on health-related quality of life.

    Br J Cancer 2004, 91:69-76. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  48. Rimer BK, Bluman LG: The psychosocial consequences of mammography.

    J Natl Cancer Inst Monogr 1997, 131-138. PubMed Abstract OpenURL

  49. Kriege M, Brekelmans CT, Boetes C, Besnard PE, Zonderland HM, Obdeijn IM, et al.: Efficacy of MRI and mammography for breast-cancer screening in women with a familial or genetic predisposition.

    N Engl J Med 2004, 351:427-437. PubMed Abstract | Publisher Full Text OpenURL

  50. Evans GR, Gaarenstroom KN, Stirling D, Shenton A, Maehle L, Dorum A, et al.: Screening for Familial Ovarian Cancer: Poor survival of BRCA1/2 related cancers.

    J Med Genet 2009, 46:593-597. PubMed Abstract | Publisher Full Text OpenURL

  51. Stirling D, Evans DG, Pichert G, Shenton A, Kirk EN, Rimmer S, et al.: Screening for familial ovarian cancer: failure of current protocols to detect ovarian cancer at an early stage according to the international Federation of gynecology and obstetrics system.

    J Clin Oncol 2005, 23:5588-5596. PubMed Abstract | Publisher Full Text OpenURL

  52. van der Velde NM, Mourits MJ, Arts HJ, de Vries J, Leegte BK, Dijkhuis G, et al.: Time to stop ovarian cancer screening in BRCA1/2 mutation carriers?

    Int J Cancer 2009, 124:919-923. PubMed Abstract | Publisher Full Text OpenURL

  53. Subramanian A, Salhab M, Mokbel K: Oestrogen producing enzymes and mammary carcinogenesis: a review.

    Breast Cancer Res Treat 2008, 111:191-202. PubMed Abstract | Publisher Full Text OpenURL

  54. Fisher B, Costantino JP, Wickerham DL, Cecchini RS, Cronin WM, Robidoux A, et al.: Tamoxifen for the prevention of breast cancer: current status of the National Surgical Adjuvant Breast and Bowel Project P-1 study.

    J Natl Cancer Inst 2005, 97:1652-1662. PubMed Abstract | Publisher Full Text OpenURL

  55. King MC, Wieand S, Hale K, Lee M, Walsh T, Owens K, et al.: Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.

    JAMA 2001, 286:2251-2256. PubMed Abstract | Publisher Full Text OpenURL

  56. Bramley M, Clarke RB, Howell A, Evans DG, Armer T, Baildam AD, et al.: Effects of oestrogens and anti-oestrogens on normal breast tissue from women bearing BRCA1 and BRCA2 mutations.

    Br J Cancer 2006, 94:1021-1028. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  57. Kote-Jarai Z, Powles TJ, Mitchell G, Tidy A, Ashley S, Easton D, et al.: BRCA1/BRCA2 mutation status and analysis of cancer family history in participants of the Royal Marsden Hospital tamoxifen chemoprevention trial.

    Cancer Lett 2007, 247:259-265. PubMed Abstract | Publisher Full Text OpenURL

  58. Calderon-Margalit R, Paltiel O: Prevention of breast cancer in women who carry BRCA1 or BRCA2 mutations: a critical review of the literature.

    Int J Cancer 2004, 112:357-364. PubMed Abstract | Publisher Full Text OpenURL

  59. Metcalfe K, Lynch HT, Ghadirian P, Tung N, Olivotto I, Warner E, et al.: Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers.

    J Clin Oncol 2004, 22:2328-2335. PubMed Abstract | Publisher Full Text OpenURL

  60. Sonnenberg FA, Beck JR: Markov models in medical decision making: a practical guide.

    Med Decis Making 1993, 13:322-338. PubMed Abstract | Publisher Full Text OpenURL

  61. Beral V, Hermon C, Kay C, Hannaford P, Darby S, Reeves G: Mortality associated with oral contraceptive use: 25 year follow up of cohort of 46 000 women from Royal College of General Practitioners' oral contraception study.

    BMJ 1999, 318:96-100. PubMed Abstract | PubMed Central Full Text OpenURL

  62. Whittemore AS, Harris R, Itnyre J: Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. II. Invasive epithelial ovarian cancers in white women. Collaborative Ovarian Cancer Group.

    Am J Epidemiol 1992, 136:1184-1203. PubMed Abstract OpenURL

  63. Narod SA, Risch H, Moslehi R, Dorum A, Neuhausen S, Olsson H, et al.: Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group.

    N Engl J Med 1998, 339:424-428. PubMed Abstract | Publisher Full Text OpenURL

  64. Breast cancer and hormonal contraceptives: collaborative reanalysis of individual data on 53 297 women with breast cancer and 100 239 women without breast cancer from 54 epidemiological studies. Collaborative Group on Hormonal Factors in Breast Cancer

    Lancet 1996, 347:1713-1727. PubMed Abstract | Publisher Full Text OpenURL

  65. De Soto JA, Deng CX: PARP-1 inhibitors: are they the long-sought genetically specific drugs for BRCA1/2-associated breast cancers?

    Int J Med Sci 2006, 3:117-123. PubMed Abstract | PubMed Central Full Text OpenURL

  66. Lerman C, Narod S, Schulman K, Hughes C, Gomez-Caminero A, Bonney G, et al.: BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.

    JAMA 1996, 275:1885-1892. PubMed Abstract | Publisher Full Text OpenURL

  67. Grann VR, Panageas KS, Whang W, Antman KH, Neugut AI: Decision analysis of prophylactic mastectomy and oophorectomy in BRCA1-positive or BRCA2-positive patients.

    J Clin Oncol 1998, 16:979-985. PubMed Abstract | Publisher Full Text OpenURL

  68. Grann VR, Jacobson JS, Whang W, Hershman D, Heitjan DF, Antman KH, et al.: Prevention with tamoxifen or other hormones versus prophylactic surgery in BRCA1/2-positive women: a decision analysis.

    Cancer J Sci Am 2000, 6:13-20. PubMed Abstract OpenURL

  69. van Roosmalen MS, Verhoef LC, Stalmeier PF, Hoogerbrugge N, van Daal WA: Decision analysis of prophylactic surgery or screening for BRCA1 mutation carriers: a more prominent role for oophorectomy.

    J Clin Oncol 2002, 20:2092-2100. PubMed Abstract | Publisher Full Text OpenURL

  70. Schrag D, Kuntz KM, Garber JE, Weeks JC: Decision analysis--effects of prophylactic mastectomy and oophorectomy on life expectancy among women with BRCA1 or BRCA2 mutations.

    N Engl J Med 1997, 336:1465-1471. PubMed Abstract | Publisher Full Text OpenURL

  71. Schrag D, Kuntz KM, Garber JE, Weeks JC: Life expectancy gains from cancer prevention strategies for women with breast cancer and BRCA1 or BRCA2 mutations.

    JAMA 2000, 283:617-624. PubMed Abstract | Publisher Full Text OpenURL

  72. Hartmann LC, Sellers TA, Schaid DJ, Frank TS, Soderberg CL, Sitta DL, et al.: Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers.

    J Natl Cancer Inst 2001, 93:1633-1637. PubMed Abstract | Publisher Full Text OpenURL

  73. Meijers-Heijboer H, van Geel B, van Putten WL, Henzen-Logmans SC, Seynaeve C, Menke-Pluymers MB, et al.: Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation.

    N Engl J Med 2001, 345:159-164. PubMed Abstract | Publisher Full Text OpenURL

  74. Rebbeck TR, Friebel T, Lynch HT, Neuhausen SL, van ' V, Garber JE, et al.: Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group.

    J Clin Oncol 2004, 22:1055-1062. PubMed Abstract | Publisher Full Text OpenURL

  75. Heemskerk-Gerritsen BA, Brekelmans CT, Menke-Pluymers MB, van Geel AN, Tilanus-Linthorst MM, Bartels CC, et al.: Prophylactic mastectomy in BRCA1/2 mutation carriers and women at risk of hereditary breast cancer: long-term experiences at the Rotterdam Family Cancer Clinic.

    Ann Surg Oncol 2007, 14:3335-3344. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  76. Tercyak KP, Peshkin BN, Brogan BM, DeMarco T, Pennanen MF, Willey SC, et al.: Quality of life after contralateral prophylactic mastectomy in newly diagnosed high-risk breast cancer patients who underwent BRCA1/2 gene testing.

    J Clin Oncol 2007, 25:285-291. PubMed Abstract | Publisher Full Text OpenURL

  77. Lodder LN, Frets PG, Trijsburg RW, Meijers-Heijboer EJ, Klijn JG, Seynaeve C, et al.: One year follow-up of women opting for presymptomatic testing for BRCA1 and BRCA2: emotional impact of the test outcome and decisions on risk management (surveillance or prophylactic surgery).

    Breast Cancer Res Treat 2002, 73:97-112. PubMed Abstract | Publisher Full Text OpenURL

  78. Markopoulos C, Tsaroucha AK, Kouskos E, Mantas D, Antonopoulou Z, Karvelis S: Impact of breast cancer surgery on the self-esteem and sexual life of female patients.

    J Int Med Res 2009, 37:182-188. PubMed Abstract | Publisher Full Text OpenURL

  79. Gahm J, Jurell G, Edsander-Nord A, Wickman M: Patient satisfaction with aesthetic outcome after bilateral prophylactic mastectomy and immediate reconstruction with implants.

    J Plast Reconstr Aesthet Surg 2010, 63:332-338. PubMed Abstract | Publisher Full Text OpenURL

  80. Patani N, Devalia H, Anderson A, Mokbel K: Oncological safety and patient satisfaction with skin-sparing mastectomy and immediate breast reconstruction.

    Surg Oncol 2008, 17:97-105. PubMed Abstract | Publisher Full Text OpenURL

  81. Cordeiro PG: Breast reconstruction after surgery for breast cancer.

    N Engl J Med 2008, 359:1590-1601. PubMed Abstract | Publisher Full Text OpenURL

  82. Sacchini V, Pinotti JA, Barros AC, Luini A, Pluchinotta A, Pinotti M, et al.: Nipple-sparing mastectomy for breast cancer and risk reduction: oncologic or technical problem?

    J Am Coll Surg 2006, 203:704-714. PubMed Abstract | Publisher Full Text OpenURL

  83. Narod SA: Hormonal prevention of hereditary breast cancer.

    Ann N Y Acad Sci 2001, 952:36-43. PubMed Abstract | Publisher Full Text OpenURL

  84. Mitrunen K, Hirvonen A: Molecular epidemiology of sporadic breast cancer. The role of polymorphic genes involved in oestrogen biosynthesis and metabolism.

    Mutat Res 2003, 544:9-41. PubMed Abstract | Publisher Full Text OpenURL

  85. Rebbeck TR, Lynch HT, Neuhausen SL, Narod SA, Van't Veer L, Garber JE, et al.: Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations.

    N Engl J Med 2002, 346:1616-1622. PubMed Abstract | Publisher Full Text OpenURL

  86. Kauff ND, Satagopan JM, Robson ME, Scheuer L, Hensley M, Hudis CA, et al.: Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation.

    N Engl J Med 2002, 346:1609-1615. PubMed Abstract | Publisher Full Text OpenURL

  87. Kauff ND, Domchek SM, Friebel TM, Robson ME, Lee J, Garber JE, et al.: Risk-reducing salpingo-oophorectomy for the prevention of B.

    J Clin Oncol 2008, 26:1331-1337. PubMed Abstract | Publisher Full Text OpenURL

  88. Chang-Claude J, Andrieu N, Rookus M, Brohet R, Antoniou AC, Peock S, et al.: Age at menarche and menopause and breast cancer risk in the International BRCA1/2 Carrier Cohort Study.

    Cancer Epidemiol Biomarkers Prev 2007, 16:740-746. PubMed Abstract | Publisher Full Text OpenURL

  89. Domchek SM, Friebel TM, Neuhausen SL, Wagner T, Evans G, Isaacs C, et al.: Mortality after bilateral salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers: a prospective cohort study.

    Lancet Oncol 2006, 7:223-229. PubMed Abstract | Publisher Full Text OpenURL

  90. Eisen A, Lubinski J, Klijn J, Moller P, Lynch HT, Offit K, et al.: Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers: an international case-control study.

    J Clin Oncol 2005, 23:7491-7496. PubMed Abstract | Publisher Full Text OpenURL

  91. Finch A, Beiner M, Lubinski J, Lynch HT, Moller P, Rosen B, et al.: Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation.

    JAMA 2006, 296:185-192. PubMed Abstract | Publisher Full Text OpenURL

  92. Kramer JL, Velazquez IA, Chen BE, Rosenberg PS, Struewing JP, Greene MH: Prophylactic oophorectomy reduces breast cancer penetrance during prospective, long-term follow-up of BRCA1 mutation carriers.

    J Clin Oncol 2005, 23:8629-8635. PubMed Abstract | Publisher Full Text OpenURL

  93. Rebbeck TR, Levin AM, Eisen A, Snyder C, Watson P, Cannon-Albright L, et al.: Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers.

    J Natl Cancer Inst 1999, 91:1475-1479. PubMed Abstract | Publisher Full Text OpenURL

  94. Rutter JL, Wacholder S, Chetrit A, Lubin F, Menczer J, Ebbers S, et al.: Gynecologic surgeries and risk of ovarian cancer in women with BRCA1 and BRCA2 Ashkenazi founder mutations: an Israeli population-based case-control study.

    J Natl Cancer Inst 2003, 95:1072-1078. PubMed Abstract | Publisher Full Text OpenURL

  95. Rebbeck TR, Kauff ND, Domchek SM: Meta-analysis of risk reduction estimates associated with risk-reducing salpingo-oophorectomy in BRCA1 or BRCA2 mutation carriers.

    J Natl Cancer Inst 2009, 101:80-87. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  96. Willsher P, Ali A, Jackson L: Laparoscopic oophorectomy in the management of breast disease.

    ANZ J Surg 2008, 78:670-672. PubMed Abstract | Publisher Full Text OpenURL

  97. Batista LI, Lu KH, Beahm EK, Arun BK, Bodurka DC, Meric-Bernstam F: Coordinated prophylactic surgical management for women with hereditary breast-ovarian cancer syndrome.

    BMC Cancer 2008, 8:101. PubMed Abstract | BioMed Central Full Text | PubMed Central Full Text OpenURL

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