Simple Summary
This study summarizes the current landscape of breast cancer risk reduction strategies in East and Southeast Asia, especially in the context of the rising interest in risk-based screening. Clinical trial results and European guidelines may not always be directly applicable to Asian populations due to differences in healthcare systems, disease prevalence, lifestyle factors, and genetic predispositions. By focusing on regional evidence, we can potentially identify gaps and areas where Asian populations may benefit from new or modified approaches. Asian evidence can inform more relevant and effective local practices.
Abstract
Breast cancer (BC) screening enables early detection and timely treatment of cancer. Improving the effectiveness of BC screening can be accomplished by personalizing screening schedules according to each woman’s specific risk level. However, when informing women about their risk classification, especially those at high risk, it is important to give clear recommendations on how to lower their risk. BC risk reduction comprises lifestyle modifications, preventive surgery, and chemoprevention, with the latter two being particularly applicable to high-risk individuals. Public health guidance on risk-reducing interventions is heterogeneous and context-dependent. We conducted a scoping review on BC surgical interventions and chemoprevention in East and Southeast Asia in publications between 2010 and 2024. We searched two databases and identified 23 publications relevant for inclusion. The highest number of publications came from South Korea (n = 9). More publications discussed surgical interventions compared to pharmacological interventions. The studies were largely observational and utilized data from medical records. Most studies defined high-risk individuals as BRCA carriers, many of whom previously had cancer. The field would benefit from randomized studies of BC prevention strategies focusing on Asian populations. Future research could explore women’s sentiments towards chemoprevention compared to prophylactic surgery and could extend the definition of high-risk individuals beyond BRCA carriers.
1. Introduction
Breast cancer is a global public health issue, responsible for approximately 25% of all cancer diagnoses among women [1]. Despite the advancements in cancer therapies, the burden of breast cancer is expected to increase in the coming years due to the rising life expectancy worldwide [2]. Prevention and early detection have thus become pillars of cancer management, with many countries having national breast cancer screening programs. Most programs involve regular mammograms for women who have passed a specific age threshold, a practice supported by randomized controlled trials (RCTs) [3,4,5,6]. However, these programs have been criticized for failing to acknowledge the individual differences in cancer risk, as it has been well established that factors such as family history, genetic mutations, estrogen exposure, BMI, physical activity, and substance use affect one’s likelihood of developing cancer [5,7,8,9,10,11,12,13,14].
In response to those critiques, there has been a growing interest in shifting from age-based to personalized screening approaches [15,16,17]. For example, many countries have been trialing screening programs that utilize genetic, medical, and lifestyle data in risk prediction models to segment women into distinct risk categories [7,12,14,18,19,20,21]. In this way, those categorized as high risk could start attending mammograms earlier or screen more frequently than those whose risk of breast cancer is low [22,23]. Although risk-based screening might be more efficient, there are ethical implications of making women aware of their risk. The knowledge of risk classification might evoke psychological distress and a desire to act on the results, so the ethical permissibility of informing one of having a high risk of cancer without explaining how to lower it might be questioned [24,25,26,27,28].
The interventions for breast cancer risk reduction are usually split into three areas: chemoprevention, prophylactic surgery, and lifestyle modifications [29]. Chemoprevention refers to the use of pharmaceuticals to mitigate cancer occurrence; for breast cancer, selective estrogen receptor modulators (e.g., tamoxifen, raloxifene) and aromatase inhibitors (e.g., anastrozole, exemestane) have been the most promising [30,31,32,33,34]. According to the UK’s National Institute for Health and Care Excellence (NICE) eligibility criteria and assuming a 25% uptake rate, it is estimated that offering risk-reducing medication to women over 50 could prevent 11 cases of breast cancer per 1000 women [17,35]. The surgical approaches to breast cancer prevention include the prophylactic removal of entire breasts (risk-reducing mastectomy, RRM) and of ovaries and fallopian tubes (risk-reducing salpingo-oophorectomy, RRSO) [36]. RRM is reported to reduce breast cancer risk by at least 95% among women with a disease-causing BRCA mutation, while RRSO is estimated to reduce breast cancer risk by approximately 50% [37,38,39,40]. When it comes to lifestyle, typical recommendations include maintaining a healthy body mass index (BMI), limiting alcohol consumption, and engaging in regular physical activity [41,42]. However, despite their proven benefits [43], lifestyle modifications may not provide sufficient reassurance to high-risk individuals, especially those whose risks are primarily driven by genetic factors, and who might therefore prefer more targeted approaches [44].
So far, most studies on chemopreventive agents for breast cancer have been conducted in Europe and the United States, making their generalizability to Asian populations uncertain [45]. For example, recent reviews on anti-cancer drugs have highlighted that the tolerance and efficacy of some chemotherapeutic drugs might differ between populations of different ancestries [46]. Additionally, there are notable differences in the presentation of breast cancer cases in Asia compared to Western countries [47]. One of the most striking discrepancies is in the age of disease onset, given that the incidence of breast cancer in Asia seems to peak when women are in their forties and fifties, compared to the sixties and seventies in the West [6,48]. This might impact the appropriateness of surgical interventions. For example, age affects how patients view the relevance of surgical interventions. Younger women may be more concerned with physical appearance and the psychological effects of surgery, whereas older women may prioritize other quality-of-life factors after the procedure [49,50,51,52]. Furthermore, differences in cultural beliefs and system-level issues, such as infrastructure and access, might affect the acceptability and availability of preventive interventions [53,54,55,56]. For example, access rates to radiotherapy are approximately 4.7% in Cambodia, 7.9% in Myanmar, and 8.7% in Indonesia [57,58,59]. This is compounded by challenges in cancer data collection systems, poor data quality, inadequate infrastructure, and limited reporting in some countries [60,61]. As a result, these countries may prioritize immediate treatment over long-term prevention strategies because they lack the reliable data needed to guide comprehensive prevention efforts.
A scoping review of literature from East and Southeast Asia on primary breast cancer prevention helps to identify region-specific gaps in research and practice. This region has unique genetic, cultural, and healthcare factors that influence prevention strategies, yet much of the current evidence is based on Western populations. The aims of this scoping review are to (1) map the nature of East and Southeast Asian publications on chemoprevention and risk-reducing surgery for breast cancer, and (2) identify potential gaps in the literature in this context, thus providing insights relevant for stakeholders involved in breast cancer screening and prevention.
2. Methods
Due to the complex and multifaceted nature of the topic, we conducted a scoping review of the literature on pharmacological and surgical interventions for reducing the risk of breast cancer in East and Southeast Asia. This approach allows us to capture the variety of study designs and disciplinary perspectives within the field, as well as to identify key concepts and gaps [62]. The review was guided by the Arksey and O’Malley framework for scoping studies, which comprises five stages: (1) identifying the research question, (2) identifying the relevant studies, (3) study selection, (4) charting the data, and (5) collating, summarizing, and reporting the results [63]. We reported this study following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) extension for scoping reviews checklist [64].
2.1. Search Strategy
The search was performed in two online databases, PubMed and Web of Science Core Collection, on 11 July 2024. PubMed provides a comprehensive coverage of medical literature, including clinical trials and observational studies. PubMed also offers advanced filtering options, making it ideal for navigating its structured database for precise queries [65]. Web of Science provides broader multidisciplinary research coverage, including both clinical and policy-based breast cancer prevention strategies [66]. We restricted the search to articles published in English since 2010 to increase the relevance of our findings [67]. The full search strategy for both databases is available in Supplementary Tables S1 and S2.
2.2. Eligibility and Study Selection
To be included in this review, studies needed to meet the following inclusion criteria: (1) be based in an East or Southeast Asian country, (2) discuss chemoprevention and/or risk-reducing surgery for breast cancer, and (3) report strategies that show potential for lowering breast cancer risk. We excluded studies that recruited only women who already had cancer, studies that paid limited or no attention to breast cancer, and those for which the full text was unavailable. The rationale for not including articles that studied only breast cancer patients was to make our findings more relevant for risk management in the context of breast cancer screening programs, which target healthy individuals. There was no restriction on the type of study design eligible for inclusion.
We exported all search results into EndNote (v 21.2 bld 19537) to remove duplicates. The unique records were then transferred to Rayyan, a web-based systematic review software, for article screening [68]. In the first round of screening, all titles and abstracts were blindly reviewed by two authors (F.A. and C.K.Y.L.). Any conflicts were resolved in a team discussion before progressing to the second round of screening. In this round, the two authors independently assessed the full texts of the remaining studies against the inclusion criteria. The authors subsequently compared their decisions and agreed on which studies aligned with the scope of this review, and noted the specific reasons for article exclusions. The screening processes were graphically summarized using a PRISMA flow diagram [69].
2.3. Data Extraction and Analysis
From the included articles, we extracted information on the title, authors, year of publication, location, aims, methods, number and characteristics of participants, risk-reduction method, and main findings. The data were charted into an extraction table in MS Excel. Having collated all the relevant information from the studies, we summarized the key findings using two approaches. First, we graphically presented the overarching features of the included studies, focusing on their geographical distribution, publication date, and type of intervention discussed. Second, we thematically grouped the studies based on the risk-reduction strategies they covered (risk-reducing surgery, chemoprevention, or both surgery and chemoprevention). We then produced a narrative account of the key messages from each group. Organizing the data this way enabled us to gauge the dominant sources of knowledge in the field, perform intra- and inter-group comparisons, and observe what evidence might be missing.
3. Results
3.1. Scope of Studies
Our search resulted in 5083 records, of which 3471 remained after de-duplication (Figure 1). Following the title and abstract screening, we assessed the full text of 52 studies for eligibility. During the first round of screening, we noted that most studies on risk reduction of breast cancer in Asia focused on dietary patterns—particularly, consumption of soy. In the second round of screening, the most common reason for the exclusion of records was a lack of focus on breast cancer (n = 9). At the end of the screening process, 23 publications were included in this review (Figure 2 and Table 1).
Figure 1.
Flowchart of included studies.
Figure 2.
Geographical distribution of articles included. The number of articles is denoted within parentheses.
Table 1.
Summary of included studies. Articles are ordered by author names. ID denotes the corresponding position of the article during the full-text screening process.
3.2. Geographical Distribution
The majority of publications were from South Korea (n = 9, IDs 4, 5, 24, 27, 30, 31, 38, 61, 63), Taiwan (n = 7, IDs 39, 53, 95, 96, 97, 111, 112), and Japan (n = 5, study IDs 28, 49, 59, 62, 110). The sample sizes reported in the included studies ranged from 1 (ID 49) to >400,000 (n = 3, IDs 95, 96, 97). All studies from Taiwan focused on women with type II diabetes and studied potential chemopreventive agents.
3.3. Study Designs and Methodologies
Most studies were retrospective cohort or case–control studies that analyzed information from existing databases (n = 16, IDs 12, 24, 27, 30, 31, 38, 39, 53, 59, 61, 62, 95, 96, 97, 111, 112). The remaining study types were cross-sectional studies (n = 4, IDs 4, 5, 37,63), a case report (ID 49), an economic evaluation (ID 110), and clinical practice guidelines (ID 28).
3.4. High-Risk Groups Targeted
Ten studies focused on cancer risk reduction among carriers of BRCA gene mutations (IDs 4, 24, 27, 30, 37, 38, 49, 59, 62, 110), and it was common for studies to compare risk-reducing behaviors of affected and unaffected BRCA carriers. Two studies included only individuals without a personal history of breast cancer (IDs 49, 63).
3.5. Prophylactic Surgery
More studies explored risk-reducing surgery as a method of prevention of breast cancer (n = 11, IDs 4, 5, 12, 24, 27, 30, 49, 59, 62, 63, 110) compared to chemoprevention (n = 9, IDs 31, 39, 53, 61, 95, 96, 97, 111, 112). Three publications discussed both approaches to risk reduction (IDs 28, 37, 38).
Studies have shown that women with a personal history of breast cancer have significantly different approaches to cancer risk reduction compared to those without (n = 5, IDs 12, 27, 30, 38, 62). In a study investigating trends in risk-reducing surgery in South Korea (ID 27), RRM was performed in 9.9% and RRSO was performed in 34.6% of affected BRCA carriers. In comparison, 1.2% and 11.9% of BRCA carriers without a history of breast cancer underwent RRM and RRSO, respectively. RRM seemed more common among younger women (IDs 37, 62, 63), while RRSO became more acceptable with increasing age (IDs 4, 30, 38). For example, study ID 4 involved 52 BRCA mutation carriers who were at least 35 years old and found that 57% opted for RRSO. Those who underwent RRSO were significantly older than those who did not. Another study (ID 12) assessed adherence to risk management recommendations among patients who received a genetic test result showing the presence of cancer-associated mutation. Adherence was defined as undergoing RRM or annual breast imaging. The study found 74% of patients to be fully adherent, but the adherence decreased with age. Similarly, ID 63 found that the intention to undergo RRM decreased with age among cancer-free Korean women carrying BRCA mutations (odds ratio [OR] 0.39; 95% CI, 0.20 to 0.74 and 0.30; 95% CI, 0.14 to 0.61, for 30–34-year-olds and 35–39-year-olds, respectively, compared to 20–24-year-olds). Study ID 5 surveyed a cohort comprising the public, cancer patients, researchers, and clinicians using hypothetical BRCA testing scenarios and reported that 36% expressed intent to undergo RRSO, while 27% expressed intent to undergo RRM. For both types of prophylactic surgery, the most common barrier to uptake was not having a personal history of breast cancer. In addition to one’s medical history, other factors that might influence the decision to undergo surgery include the perceived risk of cancer and education level (IDs 5, 24).
There have been several accounts of the rise in genetic testing and risk-reducing surgery for breast cancer, as well as changes in insurance coverage for these procedures (IDs 27, 38, 59). Risk-reducing surgeries were found to be cost-saving and more effective than surveillance among high-risk individuals (ID 110). In general, women seemed to be more open to risk-reducing surgery than chemoprevention when it came to managing their breast cancer risk (IDs 37, 38). For example, a Korean study (ID 38) involving 179 female BRCA carriers found that 10.1% received chemoprevention (olaparib, tamoxifen, or oral contraceptives), while 44.7% underwent risk-reducing surgery. However, it should be noted that tamoxifen may have limited efficacy in preventing ER-negative and triple-negative tumors, which are more common in BRCA-related cancers [91].
3.6. Chemopreventive Agents
Research on chemopreventive agents for breast cancer in Asian populations appears limited, with more observational data than randomized controlled studies. Observational evidence suggests potential risk-reducing properties for several agents, including tamoxifen (ID 31), aspirin (ID 111, 112), ACE inhibitors combined with aspirin or NSAIDs (ID 39), analgesics (ID 61), sitagliptin (ID 96), and metformin alone (ID 95) or with rosiglitazone (ID 97). The potential of statins to lower the risk of cancer was limited and the data were inconclusive (ID 53).
Out of the nine papers that studied chemoprevention, seven were based in Taiwan (IDs 39, 53, 95, 96, 97, 111, 112), and five of those included only patients with type II diabetes (IDs 95, 96, 97, 111, 112) listed in the National Health Insurance database. There was an apparent dose–response relationship between metformin use and breast cancer risk (IDs 95, 97). It is hypothesized that metformin may reduce breast cancer risk by lowering insulin levels or activating AMPK to inhibit cancer cell growth [92]. Although supported by some studies, this relationship is currently not well established, and it possibly differs based on tumor hormone receptor status and the patient’s metabolic profile [92,93]. Diabetic patients using aspirin appeared to have a decreased risk of hormone receptor-positive breast cancer (IDs 111, 112), which aligns with findings from a meta-analysis of observational studies on prophylactic aspirin intake and breast cancer risk [94]. Study ID 112 noted that a cumulative dose of more than 8600 mg of aspirin for a mean period of 8.5 years led to a reduction in the risk of HR+ cancer. Similar effects on HR– cancer were observed only if the cumulative dose of aspirin exceeded 88,900 mg.
Based on the data from 25,992 breast cancer patients and age-matched controls in Taiwan (ID 53), exposure to lovastatin, a lipophilic statin, within three years before the date of diagnosis was associated with lower odds of breast cancer (adjusted OR 0.596, 95% CI 0.497–0.714). However, no significant difference in odds ratios for breast cancer was observed for users of non-lipophilic statins such as simvastatin, pravastatin, fluvastatin, and atorvastatin.
ID 61 found an association between regular analgesic use and a lower risk of breast cancer compared with never using analgesics (hazard ratio [HR] 0.748, 95% CI: 0.614–0.912) in a sample of 6735 Korean cancer patients and cancer-free controls of working age. Chemoprevention with tamoxifen was explored in a study (ID 31) that estimated the risks and benefits of using the drug based on information from Korean medical databases. The study found that, at an average risk of breast cancer, the risk–benefit index of tamoxifen was positive only for women younger than 40.
ACE inhibitors may aid in cancer prevention by lowering angiotensin II levels, which are associated with tumor growth and angiogenesis [95]. A nation-wide Taiwanese study (ID 39) found that ACE inhibitors alone were not significantly associated with breast cancer risk. However, when combined with NSAIDs, women who were exposed to the highest cumulative doses of both drugs (more than 365 cumulative defined daily doses within their respective study period) had a lower risk of breast cancer (adjusted OR 0.60, 95% CI 0.52–0.70). Similarly, a significant reduction in breast cancer risk was observed among women exposed to the highest cumulative doses of ACE inhibitors combined with aspirin.
A commonly reported limitation of the included studies was a small sample size (n = 7, IDs 4, 12, 24, 30, 37, 49, 59). The studies that analyzed health records highlighted issues such as imprecision of record data (e.g., uncertainty around adherence to prescriptions) and a lack of information on factors that could act as confounders for the development of breast cancer, such as BMI, age of menarche, and perceived risk.
4. Discussion
The review identified 5083 studies related to breast cancer risk reduction. However, the final analysis included only 23 publications on surgical and pharmacological interventions for reducing breast cancer risk in East and Southeast Asia. Most studies were observational and retrospective, defined high-risk individuals as BRCA mutation carriers, and were more often on surgical interventions compared to chemopreventive ones. During the screening process, we excluded a substantial number of Asian publications on breast cancer prevention through dietary modification. The apparent scholarly interest in this area might be present due to the high soy consumption in Asia, which has shown protective effects against breast cancer [96]. The effect of diet on breast cancer risk has been summarized in other studies and was beyond the scope of this review [97,98].
4.1. Prevalence of Surgical Risk Reduction over Chemoprevention
Our search captured more literature on surgical than pharmaceutical breast cancer risk reduction in East and Southeast Asia. This may be due to events occurring within the publication timeframe applied to this review (years 2010–2024) that increased awareness of primary cancer prevention with surgery. For example, some papers (ID 38, 63) mentioned Angelina Jolie’s prophylactic mastectomy in 2013 and her influence on individuals with elevated risk, sometimes referred to as “the Angelina Jolie effect” [99,100,101]. Such celebrity endorsement might have contributed to prophylactic surgery becoming more well known, subsequently increasing the demand [102,103]. Insurance coverage for BRCA testing and preventive surgeries might have also contributed to increased patient and research interests in surgery. For example, study ID 59 highlighted that the uptake rate of RRSO in Japan increased up to threefold after the national insurance system covered the RRSO and RRM procedures for breast cancer patients with BRCA pathological variants in April 2020. Study ID 38 showed a similar pattern in Korea after the National Health Insurance System (NHIS) subsidized RRSO for BRCA pathogenic carriers in 2013. They also noted that insurance reimbursement of RRM for breast cancer patients with a BRCA mutation was introduced in 2017, which could incentivize uptake. The increased uptake of risk-reducing surgery has also been observed outside the Asian context, and the cost-effectiveness of such surgeries for women with an increased risk of breast cancer has been reported previously [99,104,105].
Chemopreventive clinical trials appear to be more common in Europe than in Asia, indicating a divergence in research priorities and drug development across these regions. Raloxifene, a selective estrogen receptor modulator (SERM), has been widely studied in Europe for both breast cancer prevention and osteoporosis treatment. Since 1999, trials in European countries have examined raloxifene’s impact on breast cancer cell markers like Ki67 and apoptosis [106]. In contrast, clinical trials investigating raloxifene in Asia remain sparse. A nationwide study in Korea found limited evidence supporting raloxifene’s efficacy in reducing breast cancer risk and emphasized the need for more research in Asian populations [107].
Beyond raloxifene, Europe has a broader spectrum of breast cancer chemoprevention trials, including IBIS-I (tamoxifen), IBIS-II (anastrozole), MAP.3 (exemestane), and LIBER (letrozole for BRCA mutation carriers) [108,109,110,111]. In contrast, the adoption of chemoprevention is less common in Asia, where there is greater reluctance to use preventive medications [112]. While there are some efforts, such as a tamoxifen trial in Japan and China (NCT03423199), many other drugs remain underexplored. More clinical trials and RCTs are urgently needed to strengthen chemopreventive options for high-risk populations in East and Southeast Asia.
4.2. Factors Influencing Uptake of Risk-Reducing Surgery Versus Chemoprevention
A common finding within the surgery-centered studies was that increased age was positively associated with RRSO uptake and inversely associated with RRM uptake among BRCA carriers, which is consistent with existing literature [113]. This might be partially explained by the differences in the age of onset of breast and ovarian cancer, respectively, with ovarian cancer usually being diagnosed in older patient groups [114]. Although countries covered in this review primarily base their guidance on RRSO and RRM on one’s genetic risk, there are some age-related considerations. Surgery is usually recommended for carriers of BRCA pathogenic variants who are in their late 30s and mid-40s and have completed childbearing [78]. Nonetheless, RRSO may be delayed until a woman turns 40 if she is known to carry the BRCA2 mutation and not the BRCA1 mutation, as is the case in Japan (ID 59). The included studies also confirmed that sentiments towards risk-reducing surgery differed between affected and unaffected BRCA carriers (IDs 12, 27, 30, 38, 62) and that they might be influenced by factors such as family history of cancer, cancer-related worry, and education level [115,116]. Studies that assessed both surgical prevention and chemoprevention found that surgeries and surveillance seemed to be better accepted than medication such as tamoxifen (ID 37, 38). Although randomized trials have shown that tamoxifen reduces breast cancer risk among healthy high-risk women, hesitation towards its use has been reported, partially due to its association with serious adverse events such as endometrial cancer [117,118,119,120,121,122,123,124,125]. In addition, endocrine-targeted agents are observed to reduce hormone-positive cancers but not breast cancer deaths, prompting a reassessment of current risk reduction strategies [126].
A lack of awareness might also be contributing to the suboptimal uptake of tamoxifen [127]. A UK-based multi-center survey of healthy women considering breast cancer primary prevention found that only one out of six women understood the potential benefits and harms of tamoxifen [128]. The only study in our review that focused specifically on chemoprevention with tamoxifen attempted to calculate the risk–benefit of using the drug in Korea (ID 31). The authors concluded that tamoxifen is beneficial for Korean women younger than 40, while the standard clinical guidance is to prescribe tamoxifen to women older than 35 [76,129,130]. However, the study was limited by having to rely on efficacy data of tamoxifen in the US population due to the lack of clinical trials in Korea. In addition, while tamoxifen does not appear to directly impair ovarian function, its prolonged use can delay pregnancy plans and negatively impact fertility, especially for older reproductive-aged women. Addressing fertility concerns may improve adherence to this important breast cancer treatment. The uptake and implementation of risk reduction strategies for breast cancer in East and Southeast Asia might also be shaped by sociocultural factors. Perceptions of cancer in this region are influenced by religious heterogeneity and underlying values of conservativism and collectivism [131]. For instance, a study from Malaysia found that women’s strong trust in alternative medicine and traditional healers might lead to reservations towards Western medicine, and that cultural norms of appreciating bodily integrity might discourage them from invasive procedures such as surgery [55]. Some of the additional barriers to breast-related care include fear of pain and social judgment, feeling embarrassed, beliefs that diseases such as breast cancer are predetermined and inevitable, and a lack of support from friends and family [6].
4.3. Differences in the Definition of High Risk
Coupled with the relative lack of chemoprevention efficacy data in East and Southeast Asia compared to in America and Europe, studies focusing on high-risk individuals in these regions tend to have a narrower definition of risk. Many Asian studies focus on BRCA carriers as high-risk individuals, when in fact, the risk of breast cancer is contributed to by many other attributes [132,133]. In contrast, European studies also look at other factors, such as the diagnoses of atypical ductal hyperplasia (ADH) and atypical lobular hyperplasia (ALH) [134,135]. Some studies also include healthy individuals identified to be at high risk from genetic and non-genetic risk predictors, which Asian studies often do not focus on [136,137].
4.4. Gaps and Opportunities for Research
Based on the review of the identified studies, we noted several potential gaps in the literature. Geographically, there was limited representation outside East Asia—specifically, beyond South Korea, Taiwan, and Japan. Regarding study design, experimental studies are absent, particularly RCTs on chemopreventive agents for breast cancer in Asian populations. The studies are mainly observational and retrospective (16 out of 23), limiting the ability to infer causality. Most studies focused on BRCA gene mutations. There are other definitions of high risk, such as healthy individuals classified as high risk based on non-genetic risk factors or patients diagnosed with DCIS and atypical lesions, who may also benefit from risk-reduction interventions. It is also important to acknowledge that BRCA-negative, high-risk women might have different sentiments toward the pharmaceutical and surgical prevention strategies discussed here. Regarding prophylactic interventions, while some agents like tamoxifen, aspirin, and metformin were explored, there is a lack of studies investigating newer or less commonly used chemopreventive agents, such as raloxifene, aromatase inhibitors, selective progesterone receptor modulators (SPRMs), and other nonsteroidal anti-inflammatory drugs (NSAIDs) [138,139,140,141,142,143]. There is also limited research on how different breast cancer prevention strategies impact patient quality of life, satisfaction, and overall well-being. For example, effects on body image and psyche are often overlooked and not discussed [144]. In addition, it is important to note the uncertainty surrounding the optimal duration of treatment. The long-term administration of chemopreventive agents such as anti-inflammatories, statins, or tamoxifen, particularly in high-risk, young patients, poses challenges due to potential side effects and cumulative harm. Moreover, the lack of clarity on what happens when treatment is discontinued, especially when breast cancer risk continues to increase over time, highlights the need for further investigation into the appropriate length of treatment and follow-up for these interventions.
4.5. Strengths and Limitations
Asian populations are often underrepresented in global breast cancer research. To our knowledge, this scoping review of a broad spectrum of relevant studies is the first to map the literature on surgical and pharmaceutical prevention of breast cancer in East and Southeast Asia. The review also provides an overview of various chemopreventive agents studied, or lack thereof, in Asian populations. However, the review has some limitations. Despite searching two large databases and following a standardized methodological framework, we might have missed relevant studies published elsewhere or used terminology that deviated from our search. It is also possible that some studies from East and Southeast Asia are not published in English-language journals. Several studies included in the review had small sample sizes, which can lead to reduced statistical power and may limit the generalizability of the findings. Small studies are also more prone to bias and may not adequately capture the variability in outcomes. Additionally, all included studies were observational, which should be kept in mind when interpreting the results. Worthy of note is that this study design is insufficient to prove causality between an intervention and breast cancer risk reduction.
5. Conclusions
By focusing on East and Southeast Asia, the review helps identify gaps in the research and highlights the need for randomized controlled l studies tailored to Asian populations. While such research is important for advancing long-term prevention efforts, from a primary care perspective, recommending more frequent or earlier screening for high-risk individuals is a practical approach to breast cancer risk management. Early detection, particularly when cancers are identified at an early stage, can improve treatment outcomes and may reduce the need for more aggressive therapies, such as chemotherapy or radiotherapy. Lifestyle modifications, including weight management and dietary adjustments, are also appropriate preventive measures. However, more invasive interventions, such as prophylactic chemoprevention or surgery, should be considered primarily for individuals at very high risk. There is also a need for better data quality, comprehensive reporting standards, and inclusion of underrepresented populations across the region. To advance these efforts, we recommend prioritizing well-designed randomized controlled studies that actively involve patient participants and incorporate input from healthcare professionals. Enhancing data collection methods and fostering cross-disciplinary collaborations will be essential to developing effective, evidence-based prevention strategies tailored to diverse populations.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cancers17020168/s1, Table S1: Search terms for Pubmed. Table S2: Search terms for Web of Science.
Author Contributions
Conceptualization and supervision: J.L.; methodology, literature search, screening and selection of studies, data extraction, original draft preparation: F.A. and C.K.Y.L.; clinical input: Q.Z., S.S.N.G. and M.H.; manuscript review and editing: all. All authors have read and agreed to the published version of the manuscript.
Funding
This study is funded by the Agency of Science, Technology and Research (A*STAR) and the Precision Health Research, Singapore (PRECISE), Clinical Implementation Project (BREATHE CIP).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
No dataset was used for this scoping review. All information used from published sources is listed in Table 1.
Acknowledgments
During the preparation of this work, the authors used Grammarly and ChatGPT for language editing purposes. After using this tool, the authors reviewed and edited the content as needed and take full responsibility for the content of the publication.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Lei, S.; Zheng, R.; Zhang, S.; Wang, S.; Chen, R.; Sun, K.; Zeng, H.; Zhou, J.; Wei, W. Global patterns of breast cancer incidence and mortality: A population-based cancer registry data analysis from 2000 to 2020. Cancer Commun. 2021, 41, 1183–1194. [Google Scholar] [CrossRef] [PubMed]
- Wilkinson, L.; Gathani, T. Understanding breast cancer as a global health concern. Br. J. Radiol. 2022, 95, 20211033. [Google Scholar] [CrossRef] [PubMed]
- Nelson, H.D.; Fu, R.; Cantor, A.; Pappas, M.; Daeges, M.; Humphrey, L. Effectiveness of Breast Cancer Screening: Systematic Review and Meta-analysis to Update the 2009 U.S. Preventive Services Task Force Recommendation. Ann. Intern. Med. 2016, 164, 244–255. [Google Scholar] [CrossRef] [PubMed]
- Harvey, J.A. Randomized Controlled Mammography Screening Trials Revisited. J. Breast Imaging 2022, 4, 105–107. [Google Scholar] [CrossRef] [PubMed]
- Allweis, T.M.; Hermann, N.; Berenstein-Molho, R.; Guindy, M. Personalized Screening for Breast Cancer: Rationale, Present Practices, and Future Directions. Ann. Surg. Oncol. 2021, 28, 4306–4317. [Google Scholar] [CrossRef]
- Lim, Y.X.; Lim, Z.L.; Ho, P.J.; Li, J. Breast Cancer in Asia: Incidence, Mortality, Early Detection, Mammography Programs, and Risk-Based Screening Initiatives. Cancers 2022, 14, 4218. [Google Scholar] [CrossRef]
- Clift, A.K.; Dodwell, D.; Lord, S.; Petrou, S.; Brady, S.M.; Collins, G.S.; Hippisley-Cox, J. The current status of risk-stratified breast screening. Br. J. Cancer 2022, 126, 533–550. [Google Scholar] [CrossRef] [PubMed]
- Smolarz, B.; Nowak, A.Z.; Romanowicz, H. Breast Cancer-Epidemiology, Classification, Pathogenesis and Treatment (Review of Literature). Cancers 2022, 14, 2569. [Google Scholar] [CrossRef]
- Grimm, L.J.; Avery, C.S.; Hendrick, E.; Baker, J.A. Benefits and Risks of Mammography Screening in Women Ages 40 to 49 Years. J. Prim. Care Community Health 2022, 13, 21501327211058322. [Google Scholar] [CrossRef] [PubMed]
- Paige, J.S.; Lee, C.I.; Wang, P.C.; Hsu, W.; Brentnall, A.R.; Hoyt, A.C.; Naeim, A.; Elmore, J.G. Variability Among Breast Cancer Risk Classification Models When Applied at the Level of the Individual Woman. J. Gen. Intern. Med. 2023, 38, 2584–2592. [Google Scholar] [CrossRef] [PubMed]
- Mavaddat, N.; Michailidou, K.; Dennis, J.; Lush, M.; Fachal, L.; Lee, A.; Tyrer, J.P.; Chen, T.H.; Wang, Q.; Bolla, M.K.; et al. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes. Am. J. Hum. Genet. 2019, 104, 21–34. [Google Scholar] [CrossRef] [PubMed]
- Gabrielson, M.; Eriksson, M.; Hammarstrom, M.; Borgquist, S.; Leifland, K.; Czene, K.; Hall, P. Cohort Profile: The Karolinska Mammography Project for Risk Prediction of Breast Cancer (KARMA). Int. J. Epidemiol. 2017, 46, 1740–1741g. [Google Scholar] [CrossRef] [PubMed]
- Mars, N.; Kerminen, S.; Tamlander, M.; Pirinen, M.; Jakkula, E.; Aaltonen, K.; Meretoja, T.; Heinavaara, S.; Widen, E.; Ripatti, S.; et al. Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women. J. Clin. Oncol. 2024, 42, 1477–1487. [Google Scholar] [CrossRef]
- Liu, J.; Ho, P.J.; Tan, T.H.L.; Yeoh, Y.S.; Chew, Y.J.; Mohamed Riza, N.K.; Khng, A.J.; Goh, S.A.; Wang, Y.; Oh, H.B.; et al. BREAst screening Tailored for HEr (BREATHE)-A study protocol on personalised risk-based breast cancer screening programme. PLoS ONE 2022, 17, e0265965. [Google Scholar] [CrossRef] [PubMed]
- Kerlikowske, K.; Bibbins-Domingo, K. Toward Risk-Based Breast Cancer Screening. Ann. Intern. Med. 2021, 174, 710–711. [Google Scholar] [CrossRef]
- Esserman, L.; Eklund, M.; Veer, L.V.; Shieh, Y.; Tice, J.; Ziv, E.; Blanco, A.; Kaplan, C.; Hiatt, R.; Fiscalini, A.S.; et al. The WISDOM study: A new approach to screening can and should be tested. Breast Cancer Res. Treat. 2021, 189, 593–598. [Google Scholar] [CrossRef]
- Usher-Smith, J.A.; Hindmarch, S.; French, D.P.; Tischkowitz, M.; Moorthie, S.; Walter, F.M.; Dennison, R.A.; Stutzin Donoso, F.; Archer, S.; Taylor, L.; et al. Proactive breast cancer risk assessment in primary care: A review based on the principles of screening. Br. J. Cancer 2023, 128, 1636–1646. [Google Scholar] [CrossRef]
- Esserman, L.J.; Study, W.; Athena, I. The WISDOM Study: Breaking the deadlock in the breast cancer screening debate. NPJ Breast Cancer 2017, 3, 34. [Google Scholar] [CrossRef] [PubMed]
- Shieh, Y.; Eklund, M.; Madlensky, L.; Sawyer, S.D.; Thompson, C.K.; Stover Fiscalini, A.; Ziv, E.; Van’t Veer, L.J.; Esserman, L.J.; Tice, J.A.; et al. Breast Cancer Screening in the Precision Medicine Era: Risk-Based Screening in a Population-Based Trial. J. Natl. Cancer Inst. 2017, 109, djw290. [Google Scholar] [CrossRef] [PubMed]
- Brooks, J.D.; Nabi, H.H.; Andrulis, I.L.; Antoniou, A.C.; Chiquette, J.; Despres, P.; Devilee, P.; Dorval, M.; Droit, A.; Easton, D.F.; et al. Personalized Risk Assessment for Prevention and Early Detection of Breast Cancer: Integration and Implementation (PERSPECTIVE I&I). J. Pers. Med. 2021, 11, 511. [Google Scholar] [CrossRef] [PubMed]
- Pace, L.E. Risk-Based Approaches to Breast Cancer Screening in China. JAMA Netw. Open 2022, 5, e2241448. [Google Scholar] [CrossRef]
- Bolze, A.; Cirulli, E.T.; Hajek, C.; Schnell Blitstein, J.M.; Grzymski, J.J. The Potential of Genetics in Identifying Women at Lower Risk of Breast Cancer. JAMA Oncol. 2024, 10, 236–239. [Google Scholar] [CrossRef] [PubMed]
- Bhatt, R.; van den Hout, A.; Antoniou, A.C.; Shah, M.; Ficorella, L.; Steggall, E.; Easton, D.F.; Pharoah, P.D.P.; Pashayan, N. Estimation of age of onset and progression of breast cancer by absolute risk dependent on polygenic risk score and other risk factors. Cancer 2024, 130, 1590–1599. [Google Scholar] [CrossRef]
- Kelley-Jones, C.; Scott, S.; Waller, J. UK Women’s Views of the Concepts of Personalised Breast Cancer Risk Assessment and Risk-Stratified Breast Screening: A Qualitative Interview Study. Cancers 2021, 13, 5813. [Google Scholar] [CrossRef]
- Liow, J.J.K.; Lim, Z.L.; Sim, T.M.Y.; Ho, P.J.; Goh, S.A.; Choy, S.D.; Chew, Y.J.; Tan, B.K.; Tan, V.K.M.; Hartman, M.; et al. “It Will Lead You to Make Better Decisions about Your Health”-A Focus Group and Survey Study on Women’s Attitudes towards Risk-Based Breast Cancer Screening and Personalised Risk Assessments. Curr. Oncol. 2022, 29, 9181–9198. [Google Scholar] [CrossRef] [PubMed]
- Rainey, L.; van der Waal, D.; Jervaeus, A.; Wengstrom, Y.; Evans, D.G.; Donnelly, L.S.; Broeders, M.J.M. Are we ready for the challenge of implementing risk-based breast cancer screening and primary prevention? Breast 2018, 39, 24–32. [Google Scholar] [CrossRef] [PubMed]
- Xie, Z.; Wenger, N.; Stanton, A.L.; Sepucha, K.; Kaplan, C.; Madlensky, L.; Elashoff, D.; Trent, J.; Petruse, A.; Johansen, L.; et al. Risk estimation, anxiety, and breast cancer worry in women at risk for breast cancer: A single-arm trial of personalized risk communication. Psychooncology 2019, 28, 2226–2232. [Google Scholar] [CrossRef] [PubMed]
- Lee, J.M.; Lowry, K.P.; Cott Chubiz, J.E.; Swan, J.S.; Motazedi, T.; Halpern, E.F.; Tosteson, A.N.A.; Gazelle, G.S.; Donelan, K. Breast cancer risk, worry, and anxiety: Effect on patient perceptions of false-positive screening results. Breast 2020, 50, 104–112. [Google Scholar] [CrossRef]
- Britt, K.L.; Cuzick, J.; Phillips, K.A. Key steps for effective breast cancer prevention. Nat. Rev. Cancer 2020, 20, 417–436. [Google Scholar] [CrossRef] [PubMed]
- Cuzick, J.; Sestak, I.; Bonanni, B.; Costantino, J.P.; Cummings, S.; DeCensi, A.; Dowsett, M.; Forbes, J.F.; Ford, L.; LaCroix, A.Z.; et al. Selective oestrogen receptor modulators in prevention of breast cancer: An updated meta-analysis of individual participant data. Lancet 2013, 381, 1827–1834. [Google Scholar] [CrossRef] [PubMed]
- Nelson, H.D.; Fu, R.; Griffin, J.C.; Nygren, P.; Smith, M.E.; Humphrey, L. Systematic review: Comparative effectiveness of medications to reduce risk for primary breast cancer. Ann. Intern. Med. 2009, 151, 703–715. [Google Scholar] [CrossRef] [PubMed]
- Laws, A.; Punglia, R.S. Endocrine Therapy for Primary and Secondary Prevention After Diagnosis of High-Risk Breast Lesions or Preinvasive Breast Cancer. J. Clin. Oncol. 2023, 41, 3092–3099. [Google Scholar] [CrossRef]
- Cuzick, J. Preventive therapy for cancer. Lancet Oncol. 2017, 18, e472–e482. [Google Scholar] [CrossRef]
- Hammarstrom, M.; Gabrielson, M.; Crippa, A.; Discacciati, A.; Eklund, M.; Lundholm, C.; Backlund, M.; Wengstrom, Y.; Borgquist, S.; Bergqvist, J.; et al. Side effects of low-dose tamoxifen: Results from a six-armed randomised controlled trial in healthy women. Br. J. Cancer 2023, 129, 61–71. [Google Scholar] [CrossRef] [PubMed]
- Lazzeroni, M.; Puntoni, M.; Provinciali, N.; Webber, T.B.; Briata, I.M.; D’Amico, M.; Giuliano, S.; Siri, G.; Cagnacci, S.; DeCensi, A. Estimating the magnitude of clinical benefit of systemic therapy in patients with DCIS or pre-invasive disease of the breast. Breast 2019, 48 (Suppl. S1), S39–S43. [Google Scholar] [CrossRef] [PubMed]
- Costa, M.; Saldanha, P. Risk Reduction Strategies in Breast Cancer Prevention. Eur. J. Breast Health 2017, 13, 103–112. [Google Scholar] [CrossRef] [PubMed]
- Ludwig, K.K.; Neuner, J.; Butler, A.; Geurts, J.L.; Kong, A.L. Risk reduction and survival benefit of prophylactic surgery in BRCA mutation carriers, a systematic review. Am. J. Surg. 2016, 212, 660–669. [Google Scholar] [CrossRef] [PubMed]
- Carbine, N.E.; Lostumbo, L.; Wallace, J.; Ko, H. Risk-reducing mastectomy for the prevention of primary breast cancer. Cochrane Database Syst. Rev. 2018, 4, CD002748. [Google Scholar] [CrossRef] [PubMed]
- Domchek, S.M.; Friebel, T.M.; Singer, C.F.; Evans, D.G.; Lynch, H.T.; Isaacs, C.; Garber, J.E.; Neuhausen, S.L.; Matloff, E.; Eeles, R.; et al. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality. JAMA 2010, 304, 967–975. [Google Scholar] [CrossRef] [PubMed]
- Norquist, B.M.; Swisher, E.M.; Yung, R.L. Preventing Breast Cancer in High-Risk Women: Is There Still a Role for Oophorectomy? JNCI Cancer Spectr. 2020, 4, pkz076. [Google Scholar] [CrossRef] [PubMed]
- Daly, A.A.; Rolph, R.; Cutress, R.I.; Copson, E.R. A Review of Modifiable Risk Factors in Young Women for the Prevention of Breast Cancer. Breast Cancer 2021, 13, 241–257. [Google Scholar] [CrossRef] [PubMed]
- Alsayer, R.M.; De Vol, E.B.; Almeharish, A.; Alfattani, A.; Alghamdi, A.J.; AlBehlal, L.B.; Alhaddab, S.; Altwaijri, Y. Ranking of Modifiable Lifestyle Risk Factors for Breast Cancer in Saudi Women: Population Attributable Risk and Nomogram. Breast Cancer 2024, 16, 545–554. [Google Scholar] [CrossRef]
- Neirich, L.; Yahiaoui-Doktor, M.; Lammert, J.; Basrai, M.; Seethaler, B.; Berling-Ernst, A.; Ramser, J.; Quante, A.S.; Schmidt, T.; Niederberger, U.; et al. Physical activity and Mediterranean diet as potential modulators of osteoprotegerin and soluble RANKL in gBRCA1/2 mutation carriers: Results of the lifestyle intervention pilot study LIBRE-1. Breast Cancer Res. Treat. 2021, 190, 463–475. [Google Scholar] [CrossRef]
- Cohen, S.Y.; Stoll, C.R.; Anandarajah, A.; Doering, M.; Colditz, G.A. Modifiable risk factors in women at high risk of breast cancer: A systematic review. Breast Cancer Res. 2023, 25, 45. [Google Scholar] [CrossRef] [PubMed]
- Sun, R.; Chu, Y.; Gao, Y.; Cheng, W.; Gao, S. Efficacy and safety of endocrine therapy for breast-cancer prevention in high-risk premenopausal or postmenopausal women: A Bayesian network meta-analysis of nine randomized controlled trials. Menopause 2021, 28, 589–600. [Google Scholar] [CrossRef] [PubMed]
- Ma, B.B.; Hui, E.P.; Mok, T.S. Population-based differences in treatment outcome following anticancer drug therapies. Lancet Oncol. 2010, 11, 75–84. [Google Scholar] [CrossRef]
- Yap, Y.S.; Lu, Y.S.; Tamura, K.; Lee, J.E.; Ko, E.Y.; Park, Y.H.; Cao, A.Y.; Lin, C.H.; Toi, M.; Wu, J.; et al. Insights Into Breast Cancer in the East vs the West: A Review. JAMA Oncol. 2019, 5, 1489–1496. [Google Scholar] [CrossRef]
- Leong, S.P.; Shen, Z.Z.; Liu, T.J.; Agarwal, G.; Tajima, T.; Paik, N.S.; Sandelin, K.; Derossis, A.; Cody, H.; Foulkes, W.D. Is breast cancer the same disease in Asian and Western countries? World J. Surg. 2010, 34, 2308–2324. [Google Scholar] [CrossRef] [PubMed]
- Wong, F.Y.; Tham, W.Y.; Nei, W.L.; Lim, C.; Miao, H. Age exerts a continuous effect in the outcomes of Asian breast cancer patients treated with breast-conserving therapy. Cancer Commun. 2018, 38, 39. [Google Scholar] [CrossRef]
- August, D.A.; Rea, T.; Sondak, V.K. Age-related differences in breast cancer treatment. Ann. Surg. Oncol. 1994, 1, 45–52. [Google Scholar] [CrossRef] [PubMed][Green Version]
- Ritter, M.; Ling, B.M.; Oberhauser, I.; Montagna, G.; Zehnpfennig, L.; Levy, J.; Soysal, S.D.; Castrezana, L.L.; Muller, M.; Schwab, F.D.; et al. The impact of age on patient-reported outcomes after oncoplastic versus conventional breast cancer surgery. Breast Cancer Res. Treat. 2021, 187, 437–446. [Google Scholar] [CrossRef] [PubMed]
- Vuong, B.; Jacinto, A.I.; Chang, S.B.; Kuehner, G.E.; Savitz, A.C. Contemporary Review of the Management and Treatment of Young Breast Cancer Patients. Clin. Breast Cancer 2024, 24, 663–675. [Google Scholar] [CrossRef] [PubMed]
- Murray, A.; Francks, L.; Hassanein, Z.M.; Lee, R.; Wilson, E. Breast cancer surgical decision-making. Experiences of Non-Caucasian women globally. A qualitative systematic review. Eur. J. Surg. Oncol. 2023, 49, 107109. [Google Scholar] [CrossRef] [PubMed]
- Pons-Vigues, M.; Puigpinos-Riera, R.; Rodriguez, D.; Fernandez de Sanmamed, M.J.; Pasarin, M.I.; Perez, G.; Borrell, C.; Casamitjana, M.; Benet, J. Country of origin and prevention of breast cancer: Beliefs, knowledge and barriers. Health Place 2012, 18, 1270–1281. [Google Scholar] [CrossRef]
- Abdullah, N.; Mohamed, N. Influence of cultural practices on breast cancer risks, stage at presentation and outcome in a multi-ethnic developing country. Oncol. Lett. 2021, 22, 806. [Google Scholar] [CrossRef] [PubMed]
- van Strien-Knippenberg, I.S.; Arjangi-Babetti, H.; Timmermans, D.R.M.; Schrauwen, L.; Fransen, M.P.; Melles, M.; Damman, O.C. Communicating the results of risk-based breast cancer screening through visualizations of risk: A participatory design approach. BMC Med. Inform. Decis. Mak. 2024, 24, 78. [Google Scholar] [CrossRef] [PubMed]
- Nomura, H.; Abe, A.; Fusegi, A.; Yoshimitsu, T.; Misaka, S.; Murakami, A.; Matsumoto, T.; Tsumura, S.; Kanno, M.; Aoki, Y.; et al. Impact of the coverage of risk-reducing salpingo-oophorectomy by the national insurance system for women with BRCA pathogenic variants in Japan. Sci. Rep. 2023, 13, 1018. [Google Scholar] [CrossRef] [PubMed]
- Jung, S.M.; Ryu, J.M.; Park, H.S.; Park, J.S.; Kang, E.; Lee, S.; Lee, H.B.; Youn, H.J.; Yoo, T.K.; Kim, J.; et al. Trends in Risk-Reducing Mastectomy and Risk-Reducing Salpingo-Oophorectomy in Korean Carriers of the BRCA1/2 Mutation. J. Breast Cancer 2020, 23, 647–655. [Google Scholar] [CrossRef]
- Datta, N.R.; Samiei, M.; Bodis, S. Radiation therapy infrastructure and human resources in low- and middle-income countries: Present status and projections for 2020. Int. J. Radiat. Oncol. Biol. Phys. 2014, 89, 448–457. [Google Scholar] [CrossRef] [PubMed]
- Sobue, T.; Inoue, M.; Tanaka, H. Cancer Registry and Epidemiological Study Working Group report. Jpn. J. Clin. Oncol. 2010, 40 (Suppl. S1), i76–i81. [Google Scholar] [CrossRef]
- Lim, J.F.Y.; Zafra, M.; Mocanu, J.D.; Umareddy, I.; de Lima Lopes, G.; Foo, R.; Jha, A.; Hickinbotham, L. Preparing health systems in Southeast and East Asia for new paradigms of care/personalized medicine in cancers: Are health systems ready for evolving cancer management? J. Asian Public Policy 2016, 10, 268–286. [Google Scholar] [CrossRef]
- Munn, Z.; Peters, M.D.J.; Stern, C.; Tufanaru, C.; McArthur, A.; Aromataris, E. Systematic review or scoping review? Guidance for authors when choosing between a systematic or scoping review approach. BMC Med. Res. Methodol. 2018, 18, 143. [Google Scholar] [CrossRef] [PubMed]
- Arksey, H.; O’Malley, L. Scoping studies: Towards a methodological framework. Int. J. Soc. Res. Methodol. 2005, 8, 19–32. [Google Scholar] [CrossRef]
- Tricco, A.C.; Lillie, E.; Zarin, W.; O’Brien, K.K.; Colquhoun, H.; Levac, D.; Moher, D.; Peters, M.D.J.; Horsley, T.; Weeks, L.; et al. PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation. Ann. Intern. Med. 2018, 169, 467–473. [Google Scholar] [CrossRef] [PubMed]
- Gusenbauer, M.; Haddaway, N.R. Which academic search systems are suitable for systematic reviews or meta-analyses? Evaluating retrieval qualities of Google Scholar, PubMed, and 26 other resources. Res. Synth. Methods 2020, 11, 181–217. [Google Scholar] [CrossRef] [PubMed]
- Momani, S.M.; Malkawi, L.W.; AlRyalat, S.A.S. Comparing Bibliometric Analysis Using PubMed, Scopus, and Web of Science Databases. J. Vis. Exp. 2019, 152, e58494. [Google Scholar] [CrossRef]
- Helbach, J.; Pieper, D.; Mathes, T.; Rombey, T.; Zeeb, H.; Allers, K.; Hoffmann, F. Restrictions and their reporting in systematic reviews of effectiveness: An observational study. BMC Med. Res. Methodol. 2022, 22, 230. [Google Scholar] [CrossRef] [PubMed]
- Valizadeh, A.; Moassefi, M.; Nakhostin-Ansari, A.; Hosseini Asl, S.H.; Saghab Torbati, M.; Aghajani, R.; Maleki Ghorbani, Z.; Faghani, S. Abstract screening using the automated tool Rayyan: Results of effectiveness in three diagnostic test accuracy systematic reviews. BMC Med. Res. Methodol. 2022, 22, 160. [Google Scholar] [CrossRef]
- Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
- Chae, S.; Kim, E.-K.; Jang, Y.R.; Lee, A.S.; Kim, S.K.; Suh, D.H.; Kim, K.; No, J.H.; Kim, Y.-B.; Kim, S.-W.; et al. Effect of risk-reducing salpingo-oophorectomy on the quality of life in Korean BRCA mutation carriers. Asian J. Surg. 2021, 44, 1056–1062. [Google Scholar] [CrossRef]
- Chang, Y.J.; Cho, S.; Joo, J.; Ryu, K.H.; Lee, S.; Cho, J.; Lim, M.C.; Jung, S.-Y.; Han, J.H.; Lee, E.S.; et al. Differences in Willingness to Undergo BRCA1/2 Testing and Risk Reducing Surgery among the General Public, Cancer Patients, and Healthcare Professionals: A Large Population-Based Survey. J. Pers. Med. 2022, 12, 818. [Google Scholar] [CrossRef]
- Courtney, E.; Chin, X.W.; Yuen, J.; Li, S.-T.; Chen, Y.; Allen, J.C.; Tan, V.; Lim, G.H.; Ngeow, J. Risk management adherence following genetic testing for hereditary cancer syndromes: A Singaporean experience. Fam. Cancer 2018, 17, 621–626. [Google Scholar] [CrossRef]
- Jeon, H.J.; Park, H.S.; Park, J.S.; Nam, E.J.; Lee, S.-T.; Han, J. Trends in contralateral prophylactic mastectomy rate according to clinicopathologic and socioeconomic status. Ann. Surg. Treat. Res. 2019, 97. [Google Scholar] [CrossRef] [PubMed]
- Kawai, M.; Ohtani, S.; Iwasaki, M.; Yamamoto, S.; Takamatsu, K.; Okamura, H.; Arai, M.; Nomura, T.; Ozaki, S.; Shibata, K.-i.; et al. The Japanese Breast Cancer Society clinical practice guidelines for epidemiology and prevention of breast cancer, 2022 edition. Breast Cancer 2023, 31, 166–178. [Google Scholar] [CrossRef]
- Kim, D.; Kang, E.; Hwang, E.; Sun, Y.; Hwang, Y.; Yom, C.K.; Kim, K.; No, J.H.; Kim, Y.-B.; Kim, S.-W. Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation. Fam. Cancer 2013, 12, 621–628. [Google Scholar] [CrossRef]
- Kim, D.U.; Min, J.W.; Kim, Y.M.; Chang, M.C. Estimating the risks and benefits of tamoxifen for prophylactic breast cancer chemoprevention in Korea. J. Breast Cancer 2012, 15, 51–56. [Google Scholar] [CrossRef]
- Kwong, A.; Wong, C.H.N.; Shea, C.; Suen, D.T.K.; Choi, C.L.Y. Choice of Management of Southern Chinese BRCA Mutation Carriers. World J. Surg. 2010, 34, 1416–1426. [Google Scholar] [CrossRef] [PubMed]
- Lee, E.-G.; Kang, H.J.; Lim, M.C.; Park, B.; Park, S.J.; Jung, S.-Y.; Lee, S.; Kang, H.-S.; Park, S.-Y.; Park, B.; et al. Different Patterns of Risk Reducing Decisions in Affected or Unaffected BRCA Pathogenic Variant Carriers. Cancer Res. Treat. 2019, 51, 280–288. [Google Scholar] [CrossRef] [PubMed]
- Lee, H.-H.; Tsan, Y.-T.; Ho, W.-C.; Lin, M.-H.; Lee, C.-H.; Tseng, C.-D.; Guo, Y.-L.; Wang, J.-D.; Chen, P.-C. Angiotensin-converting enzyme inhibitors enhance the effect of cyclooxygenase inhibitors on breast cancer. J. Hypertens. 2012, 30, 2432–2439. [Google Scholar] [CrossRef] [PubMed]
- Maeshima, Y.; Oseto, K.; Katsuragi, R.; Yoshimoto, Y.; Takahara, S.; Yamauchi, A. Experience with Bilateral Risk-Reducing Mastectomy for an Unaffected BRCA Mutation Carrier. J. Breast Cancer 2016, 19. [Google Scholar] [CrossRef] [PubMed]
- Murakami, R.; Chen, C.; Lyu, S.-Y.; Lin, C.-E.; Tzeng, P.-C.; Wang, T.-F.; Chang, J.-C.; Shieh, Y.-H.; Chen, I.F.; Huang, S.K.; et al. Lovastatin lowers the risk of breast cancer: A population-based study using logistic regression with a random effects model. SpringerPlus 2016, 5, 1932. [Google Scholar] [CrossRef] [PubMed]
- Oh, H.S.; Seo, H.J. Association between WHO First-Step Analgesic Use and Risk of Breast Cancer in Women of Working Age. Pharm. 2023, 16, 323. [Google Scholar] [CrossRef] [PubMed]
- Ohsumi, S.; Nakamura, S.; Miyata, H.; Watanabe, C.; Den, H.; Arai, M. Risk-reducing mastectomy for women with hereditary breast and ovarian cancer (HBOC): Analytical results of data from the Japanese Organization of HBOC. Jpn. J. Clin. Oncol. 2022. [Google Scholar] [CrossRef] [PubMed]
- Park, B.; Kim, D.; Kim, J.; Lee, B.Y.; Yoon, J.; Kim, S.-W. Attitudes toward Risk-Reducing Mastectomy and Risk-Reducing Salpingo-oophorectomy among Young, Unmarried, Healthy Women in Korea. Cancer Res. Treat. 2022, 54, 375–382. [Google Scholar] [CrossRef] [PubMed]
- Tseng, C.-H. Metformin may reduce breast cancer risk in Taiwanese women with type 2 diabetes. Breast Cancer Res. Treat. 2014, 145, 785–790. [Google Scholar] [CrossRef]
- Tseng, C.-H. Sitagliptin May Reduce Breast Cancer Risk in Women With Type 2 Diabetes. Clin. Breast Cancer 2017, 17, 211–218. [Google Scholar] [CrossRef] [PubMed]
- Tseng, C.-H. Rosiglitazone reduces breast cancer risk in Taiwanese female patients with type 2 diabetes mellitus. Oncotarget 2016, 8, 3042–3048. [Google Scholar] [CrossRef] [PubMed][Green Version]
- Yamauchi, H.; Nakagawa, C.; Kobayashi, M.; Kobayashi, Y.; Mano, T.; Nakamura, S.; Arai, M. Cost-effectiveness of surveillance and prevention strategies in BRCA1/2 mutation carriers. Breast Cancer 2017, 25, 141–150. [Google Scholar] [CrossRef] [PubMed]
- Yang, Y.-S.; Kornelius, E.; Chiou, J.-Y.; Lai, Y.-R.; Lo, S.-C.; Peng, C.-H.; Huang, C.-N. Low-Dose Aspirin Reduces Breast Cancer Risk in Women with Diabetes: A Nationwide Retrospective Cohort Study in Taiwan. J. Women’s Health 2017, 26, 1278–1284. [Google Scholar] [CrossRef]
- Yang, Y.-S.; Kornelius, E.; Lo, S.-C.; Wang, Y.-H.; Huang, C.-N. Aspirin and Risk of Specific Breast Cancer Subtype in Women with Diabetes. J. Women’s Health 2023, 32, 341–346. [Google Scholar] [CrossRef] [PubMed]
- Campbell, A.M.; Morris, M.; Gallagher, R.; Boyd, R.; Carson, H.; Harkin, D.P.; Wielogorska, E.; Elliott, C.; Savage, K.I.; McIntosh, S.A. Chemoprevention in BRCA1 mutation carriers (CIBRAC): Protocol for an open allocation crossover feasibility trial assessing mechanisms of chemoprevention with goserelin and anastrozole versus tamoxifen and acceptability of treatment. BMJ Open 2018, 8, e023115. [Google Scholar] [CrossRef] [PubMed]
- Park, Y.M.; Bookwalter, D.B.; O’Brien, K.M.; Jackson, C.L.; Weinberg, C.R.; Sandler, D.P. A prospective study of type 2 diabetes, metformin use, and risk of breast cancer. Ann. Oncol. 2021, 32, 351–359. [Google Scholar] [CrossRef]
- Corleto, K.A.; Strandmo, J.L.; Giles, E.D. Metformin and Breast Cancer: Current Findings and Future Perspectives from Preclinical and Clinical Studies. Pharmaceuticals 2024, 17, 396. [Google Scholar] [CrossRef] [PubMed]
- Bakierzynska, M.; Cullinane, M.C.; Redmond, H.P.; Corrigan, M. Prophylactic aspirin intake and breast cancer risk; A systematic review and meta-analysis of observational cohort studies. Eur. J. Surg. Oncol. 2023, 49, 106940. [Google Scholar] [CrossRef] [PubMed]
- Rosenthal, T.; Gavras, I. Renin–Angiotensin Inhibition in Combating Malignancy: A Review. Anticancer Res. 2019, 39, 4597–4602. [Google Scholar] [CrossRef] [PubMed]
- Buja, A.; Pierbon, M.; Lago, L.; Grotto, G.; Baldo, V. Breast Cancer Primary Prevention and Diet: An Umbrella Review. Int. J. Environ. Res. Public Health 2020, 17, 4731. [Google Scholar] [CrossRef] [PubMed]
- Mourouti, N.; Kontogianni, M.D.; Papavagelis, C.; Panagiotakos, D.B. Diet and breast cancer: A systematic review. Int. J. Food Sci. Nutr. 2015, 66, 1–42. [Google Scholar] [CrossRef]
- De Cicco, P.; Catani, M.V.; Gasperi, V.; Sibilano, M.; Quaglietta, M.; Savini, I. Nutrition and Breast Cancer: A Literature Review on Prevention, Treatment and Recurrence. Nutrients 2019, 11, 1514. [Google Scholar] [CrossRef]
- Basu, N.N.; Hodson, J.; Chatterjee, S.; Gandhi, A.; Wisely, J.; Harvey, J.; Highton, L.; Murphy, J.; Barnes, N.; Johnson, R.; et al. The Angelina Jolie effect: Contralateral risk-reducing mastectomy trends in patients at increased risk of breast cancer. Sci. Rep. 2021, 11, 2847. [Google Scholar] [CrossRef]
- Grandjean, B.; Scherz, A.; Rabaglio, M. Eleven Years of Oncogenetic Consultations in a Swiss Center: Patient and Testing Characteristics. Appl. Clin. Genet. 2023, 16, 205–213. [Google Scholar] [CrossRef] [PubMed]
- Liede, A.; Cai, M.; Crouter, T.F.; Niepel, D.; Callaghan, F.; Evans, D.G. Risk-reducing mastectomy rates in the US: A closer examination of the Angelina Jolie effect. Breast Cancer Res. Treat. 2018, 171, 435–442. [Google Scholar] [CrossRef] [PubMed]
- Nagashima, M.; Ishikawa, T.; Asami, Y.; Hirose, Y.; Shimada, K.; Miyagami, S.; Mimura, T.; Miyamoto, S.; Onuki, M.; Morioka, M.; et al. Risk-reducing salpingo-oophorectomy for Japanese women with hereditary breast and ovarian cancer: A single-institution 10-year experience. Jpn. J. Clin. Oncol. 2023, 53, 472–479. [Google Scholar] [CrossRef]
- Arslan, B.; Tazeoglu, D.; Dag, A.; Berkesoglu, M.; Ozdemir, A.A. Is there an increasing trend of risk-reducing prophylactic mastectomy procedure in preventing breast cancer among women? Turk. J. Surg. 2021, 37, 347–354. [Google Scholar] [CrossRef] [PubMed]
- Robertson, S.A.; Summerhayes, C.M.; Laws, S.; Rainsbury, R.M. Resource implications of risk-reducing mastectomy and reconstruction. Eur. J. Surg. Oncol. 2016, 42, 45–50. [Google Scholar] [CrossRef] [PubMed]
- Wei, X.; Oxley, S.; Sideris, M.; Kalra, A.; Sun, L.; Yang, L.; Legood, R.; Manchanda, R. Cost-Effectiveness of Risk-Reducing Surgery for Breast and Ovarian Cancer Prevention: A Systematic Review. Cancers 2022, 14, 6117. [Google Scholar] [CrossRef]
- Dowsett, M.; Bundred, N.J.; Decensi, A.; Sainsbury, R.C.; Lu, Y.; Hills, M.J.; Cohen, F.J.; Veronesi, P.; O’Brien, M.E.; Scott, T.; et al. Effect of raloxifene on breast cancer cell Ki67 and apoptosis: A double-blind, placebo-controlled, randomized clinical trial in postmenopausal patients. Cancer Epidemiol. Biomark. Prev. 2001, 10, 961–966. [Google Scholar]
- Lee, J.; Lee, J.S.; Lee, J.E.; Kim, Z.; Han, S.W.; Hur, S.M.; Choi, Y.J.; Park, S. A Nationwide Study on the Incidence of Breast Cancer in Korean Women with Osteoporosis Receiving Raloxifene Treatment. J. Breast Cancer 2021, 24, 280–288. [Google Scholar] [CrossRef]
- Cuzick, J.; Forbes, J.; Edwards, R.; Baum, M.; Cawthorn, S.; Coates, A.; Hamed, A.; Howell, A.; Powles, T.; IBIS investigators. First results from the International Breast Cancer Intervention Study (IBIS-I): A randomised prevention trial. Lancet 2002, 360, 817–824. [Google Scholar] [CrossRef] [PubMed]
- Cuzick, J.; Sestak, I.; Forbes, J.F.; Dowsett, M.; Cawthorn, S.; Mansel, R.E.; Loibl, S.; Bonanni, B.; Evans, D.G.; Howell, A.; et al. Use of anastrozole for breast cancer prevention (IBIS-II): Long-term results of a randomised controlled trial. Lancet 2020, 395, 117–122. [Google Scholar] [CrossRef] [PubMed]
- Richardson, H.; Johnston, D.; Pater, J.; Goss, P. The National Cancer Institute of Canada Clinical Trials Group MAP.3 trial: An international breast cancer prevention trial. Curr. Oncol. 2007, 14, 89–96. [Google Scholar] [CrossRef] [PubMed]
- Pujol, P.; Lasset, C.; Berthet, P.; Dugast, C.; Delaloge, S.; Fricker, J.P.; Tennevet, I.; Chabbert-Buffet, N.; This, P.; Baudry, K.; et al. Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/2 mutations carriers: The LIBER trial. Fam. Cancer 2012, 11, 77–84. [Google Scholar] [CrossRef]
- Iwuji, C.; Howells, L.; Thomasset, S.; Brown, K.; Steward, W.; Barwell, J.; Thomas, A. Cancer chemoprevention: Factors influencing attitudes towards chemopreventive agents in high-risk populations. Eur. J. Cancer Prev. 2014, 23, 594–601. [Google Scholar] [CrossRef]
- Garcia, C.; Wendt, J.; Lyon, L.; Jones, J.; Littell, R.D.; Armstrong, M.A.; Raine-Bennett, T.; Powell, C.B. Risk management options elected by women after testing positive for a BRCA mutation. Gynecol. Oncol. 2014, 132, 428–433. [Google Scholar] [CrossRef]
- van der Kolk, D.M.; de Bock, G.H.; Leegte, B.K.; Schaapveld, M.; Mourits, M.J.E.; de Vries, J.; van der Hout, A.H.; Oosterwijk, J.C. Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: High cancer incidence at older age. Breast Cancer Res. Treat. 2010, 124, 643–651. [Google Scholar] [CrossRef] [PubMed]
- Wei, G.; Kumar, A.; Lee, M.C.; Wang, X. Influential Factors on Risk-reduction Mastectomy in a High-risk Breast Cancer Population With Genetic Predispositions. Clin. Breast Cancer 2021, 21, e427–e433. [Google Scholar] [CrossRef] [PubMed]
- Henry, D.A.; Lee, M.C.; Almanza, D.; Ahmed, K.A.; Sun, W.; Boulware, D.C.; Laronga, C. Trends in use of bilateral prophylactic mastectomy vs high-risk surveillance in unaffected carriers of inherited breast cancer syndromes in the Inherited Cancer Registry (ICARE). Breast Cancer Res. Treat. 2019, 174, 39–45. [Google Scholar] [CrossRef]
- Nazarali, S.A.; Narod, S.A. Tamoxifen for women at high risk of breast cancer. Breast Cancer 2014, 6, 29–36. [Google Scholar] [CrossRef]
- Brown, K. Breast cancer chemoprevention: Risk-benefit effects of the antioestrogen tamoxifen. Expert Opin. Drug Saf. 2002, 1, 253–267. [Google Scholar] [CrossRef] [PubMed]
- Fisher, B.; Costantino, J.P.; Wickerham, D.L.; Cecchini, R.S.; Cronin, W.M.; Robidoux, A.; Bevers, T.B.; Kavanah, M.T.; Atkins, J.N.; Margolese, R.G.; 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. [Google Scholar] [CrossRef]
- Nayfield, S.G.; Karp, J.E.; Ford, L.G.; Dorr, F.A.; Kramer, B.S. Potential role of tamoxifen in prevention of breast cancer. J. Natl. Cancer Inst. 1991, 83, 1450–1459. [Google Scholar] [CrossRef]
- Powles, T.J.; Ashley, S.; Tidy, A.; Smith, I.E.; Dowsett, M. Twenty-year follow-up of the Royal Marsden randomized, double-blinded tamoxifen breast cancer prevention trial. J. Natl. Cancer Inst. 2007, 99, 283–290. [Google Scholar] [CrossRef] [PubMed]
- Cuzick, J.; Forbes, J.F.; Sestak, I.; Cawthorn, S.; Hamed, H.; Holli, K.; Howell, A.; International Breast Cancer Intervention Study, I.I. Long-term results of tamoxifen prophylaxis for breast cancer--96-month follow-up of the randomized IBIS-I trial. J. Natl. Cancer Inst. 2007, 99, 272–282. [Google Scholar] [CrossRef] [PubMed]
- Veronesi, U.; Maisonneuve, P.; Rotmensz, N.; Bonanni, B.; Boyle, P.; Viale, G.; Costa, A.; Sacchini, V.; Travaglini, R.; D’Aiuto, G.; et al. Tamoxifen for the prevention of breast cancer: Late results of the Italian Randomized Tamoxifen Prevention Trial among women with hysterectomy. J. Natl. Cancer Inst. 2007, 99, 727–737. [Google Scholar] [CrossRef] [PubMed]
- Flippo-Morton, T.; Walsh, K.; Chambers, K.; Amacker-North, L.; White, B.; Sarantou, T.; Boselli, D.M.; White, R.L., Jr. Surgical Decision Making in the BRCA-Positive Population: Institutional Experience and Comparison with Recent Literature. Breast J. 2016, 22, 35–44. [Google Scholar] [CrossRef] [PubMed]
- Padamsee, T.J.; Hils, M.; Muraveva, A. Understanding low chemoprevention uptake by women at high risk of breast cancer: Findings from a qualitative inductive study of women’s risk-reduction experiences. BMC Womens Health 2021, 21, 157. [Google Scholar] [CrossRef]
- Chlebowski, R.T.; Aragaki, A.K.; Pan, K. Breast Cancer Prevention: Time for Change. JCO Oncol. Pract. 2021, 17, 709–716. [Google Scholar] [CrossRef] [PubMed]
- Thorneloe, R.J.; Hall, L.H.; Walter, F.M.; Side, L.; Lloyd, K.E.; Smith, S.G.; Investigators, E. Knowledge of Potential Harms and Benefits of Tamoxifen among Women Considering Breast Cancer Preventive Therapy. Cancer Prev. Res. 2020, 13, 411–422. [Google Scholar] [CrossRef]
- Lee, S.I.; Curtis, H.; Qureshi, S.; Dutton, B.; Qureshi, N. Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: A cross-sectional survey in England. J. Community Genet. 2021, 12, 111–120. [Google Scholar] [CrossRef] [PubMed]
- Nichols, H.B.; DeRoo, L.A.; Scharf, D.R.; Sandler, D.P. Risk-benefit profiles of women using tamoxifen for chemoprevention. J. Natl. Cancer Inst. 2015, 107, 354. [Google Scholar] [CrossRef]
- US Preventive Services Task Force Recommendation Statement; Owens, D.K.; Davidson, K.W.; Krist, A.H.; Barry, M.J.; Cabana, M.; Caughey, A.B.; Doubeni, C.A.; Epling, J.W., Jr.; Kubik, M.; et al. Medication Use to Reduce Risk of Breast Cancer: US Preventive Services Task Force Recommendation Statement. JAMA 2019, 322, 857–867. [Google Scholar] [CrossRef]
- Arevalo, M.V.P.N.; Maslog, E.A.S.; Manlongat, K.D.; Ornos, E.D.B.; Chitapanarux, I.; Eala, M.A.B.; Dee, E.C. Social determinants of sex disparities in cancer in Southeast Asia. iScience 2023, 26, 107110. [Google Scholar] [CrossRef]
- Yoon, S.Y.; Thong, M.K.; Taib, N.A.; Yip, C.H.; Teo, S.H. Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: An observational descriptive study. Fam. Cancer 2011, 10, 199–205. [Google Scholar] [CrossRef]
- Kwong, A. Genetic testing for hereditary breast cancer in Asia-moving forward. Chin. Clin. Oncol. 2016, 5, 47. [Google Scholar] [CrossRef] [PubMed]
- Nicosia, L.; Mariano, L.; Pellegrino, G.; Ferrari, F.; Pesapane, F.; Bozzini, A.C.; Frassoni, S.; Bagnardi, V.; Pupo, D.; Mazzarol, G.; et al. Atypical Ductal Hyperplasia and Lobular In Situ Neoplasm: High-Risk Lesions Challenging Breast Cancer Prevention. Cancers 2024, 16, 837. [Google Scholar] [CrossRef]
- Sanders, M.E.; Podoll, M.B. Atypical Ductal Hyperplasia-Ductal Carcinoma In Situ Spectrum: Diagnostic Considerations and Treatment Impact in the Era of Deescalation. Surg. Pathol. Clin. 2022, 15, 95–103. [Google Scholar] [CrossRef] [PubMed]
- Eriksson, M.; Czene, K.; Strand, F.; Zackrisson, S.; Lindholm, P.; Lang, K.; Fornvik, D.; Sartor, H.; Mavaddat, N.; Easton, D.; et al. Identification of Women at High Risk of Breast Cancer Who Need Supplemental Screening. Radiology 2020, 297, 327–333. [Google Scholar] [CrossRef] [PubMed]
- Hietala, M.; Olsson, H.; Jernstrom, H. Prolactin levels, breast-feeding and milk production in a cohort of young healthy women from high-risk breast cancer families: Implications for breast cancer risk. Fam. Cancer 2008, 7, 221–228. [Google Scholar] [CrossRef] [PubMed]
- Cummings, S.R.; Eckert, S.; Krueger, K.A.; Grady, D.; Powles, T.J.; Cauley, J.A.; Norton, L.; Nickelsen, T.; Bjarnason, N.H.; Morrow, M.; et al. The effect of raloxifene on risk of breast cancer in postmenopausal women: Results from the MORE randomized trial. Multiple Outcomes of Raloxifene Evaluation. JAMA 1999, 281, 2189–2197. [Google Scholar] [CrossRef]
- Cauley, J.A.; Norton, L.; Lippman, M.E.; Eckert, S.; Krueger, K.A.; Purdie, D.W.; Farrerons, J.; Karasik, A.; Mellstrom, D.; Ng, K.W.; et al. Continued breast cancer risk reduction in postmenopausal women treated with raloxifene: 4-year results from the MORE trial. Multiple outcomes of raloxifene evaluation. Breast Cancer Res. Treat. 2001, 65, 125–134. [Google Scholar] [CrossRef]
- Mocellin, S.; Goodwin, A.; Pasquali, S. Risk-reducing medications for primary breast cancer: A network meta-analysis. Cochrane Database Syst. Rev. 2019, 4, CD012191. [Google Scholar] [CrossRef]
- Serrano, D.; Gandini, S.; Thomas, P.; Crew, K.D.; Kumar, N.B.; Vornik, L.A.; Lee, J.J.; Veronesi, P.; Viale, G.; Guerrieri-Gonzaga, A.; et al. Efficacy of Alternative Dose Regimens of Exemestane in Postmenopausal Women With Stage 0 to II Estrogen Receptor-Positive Breast Cancer: A Randomized Clinical Trial. JAMA Oncol. 2023, 9, 664–672. [Google Scholar] [CrossRef] [PubMed]
- Islam, M.S.; Afrin, S.; Jones, S.I.; Segars, J. Selective Progesterone Receptor Modulators-Mechanisms and Therapeutic Utility. Endocr. Rev. 2020, 41, bnaa012. [Google Scholar] [CrossRef] [PubMed]
- Moris, D.; Kontos, M.; Spartalis, E.; Fentiman, I.S. The Role of NSAIDs in Breast Cancer Prevention and Relapse: Current Evidence and Future Perspectives. Breast Care 2016, 11, 339–344. [Google Scholar] [CrossRef] [PubMed]
- Nangia, J.R.; Rimawi, M.F. Breast Cancer Prevention: Where Are We? JCO Oncol. Pract. 2021, 17, 720–722. [Google Scholar] [CrossRef] [PubMed]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).