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CME/CE

Drugs to Reduce Breast Cancer Risk: Updated Guidelines

  • Authors: News Author: Zosia Chustecka
    CME Author: Charles P. Vega, MD, FAAFP
  • CME/CE Released: 10/21/2013
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 10/21/2014
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Target Audience and Goal Statement

This article is intended for primary care clinicians, obstetrician-gynecologists, oncologists, and other specialists who care for women at risk for breast cancer.

The goal of this activity is to provide medical news to primary care clinicians and other healthcare professionals in order to enhance patient care.

Upon completion of this activity, participants will be able to:

  1. Describe the epidemiology and mortality outcomes of breast cancer.
  2. Distinguish current recommendations regarding the use of medications to prevent primary breast cancer among women.


Disclosures

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Medscape, LLC, encourages Authors to identify investigational products or off-label uses of products regulated by the US Food and Drug Administration, at first mention and where appropriate in the content.


Author(s)

  • Zosia Chustecka

    Zosia Chustecka is the News Editor for Medscape Oncology. A pharmacology graduate based in London, UK, she has edited and written extensively for publications aimed at clinician audiences. Winner of a 2011 Award for Excellence in Urology Health Reporting for an article on prostate cancer, her work also has been recognized by the British Medical Journalists Association, and recently she was awarded a Harvard University Fellowship on Cancer Genetics (May 2011) as well as a US National Press Foundation Cancer Issues Fellowship (October 2010). She can be reached at [email protected]

    Disclosures

    Disclosure: Zosia Chustecka has disclosed no relevant financial relationships.

Editor(s)

  • Amy Nadel

    Disclosures

    Disclosure: Amy Nadel has disclosed no relevant financial relationships.

CME Author(s)

  • Charles P. Vega, MD, FAAFP

    Associate Professor and Residency Director, Department of Family Medicine, University of California-Irvine, Irvine

    Disclosures

    Disclosure: Charles P. Vega, MD, FAAFP, has disclosed no relevant financial relationships.

CME Reviewer(s)

  • Yullee C. Chui

    Program Manager, Medscape, LLC

    Disclosures

    Disclosure: Yullee C. Chui has disclosed no relevant financial relationships.


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CME/CE

Drugs to Reduce Breast Cancer Risk: Updated Guidelines

Authors: News Author: Zosia Chustecka CME Author: Charles P. Vega, MD, FAAFPFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME/CE Released: 10/21/2013

Valid for credit through: 10/21/2014

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Clinical Context

Breast cancer is the most common nonskin cancer among women in the United States. According to the authors of the current guidelines, the lifetime prevalence of breast cancer among women is a striking 12.4%, with the median age at the time of diagnosis being 61 years.

The age-adjusted mortality rate associated with breast cancer is 23.0 deaths per 100,000 women per year. However, multiple factors influence the mortality risk associated with breast cancer, including race. African American women are at particularly high risk for breast cancer mortality.

Primary prevention with either tamoxifen or raloxifene is an option for the small fraction of women at very elevated risk for breast cancer. The US Preventive Services Task Force (USPSTF) critically evaluates this approach in its current guidelines.

Study Synopsis and Perspective

The USPSTF has now issued final recommendations on chemoprevention for women at high risk for breast cancer in a report published online September 24 in the Annals of Internal Medicine.

This final version follows an earlier draft of these recommendations, published in April alongside a systematic review of the literature, which found a "broad benefit" from prophylactic use of tamoxifen or raloxifene in women who had never had breast cancer.

Data from clinical trials showed that tamoxifen reduced the incidence of invasive breast cancer by 7 cases in 1000 women during 5 years, compared with placebo, and that raloxifene reduced the incidence by 9 cases. Both drugs also reduced the incidence of fractures, but both were associated with adverse events, including thromboembolic events, cataracts, and an increased risk for endometrial cancer.

The USPSTF recommends that clinicians "engage in shared, informed decision making for women who are at increased risk for breast cancer about medications to reduce their risk."

"For women who are at an increased risk of breast cancer and at low risk for adverse medication effects, clinicians should offer to prescribe risk-reducing medications, such as tamoxifen or raloxifene," the task force states. This is a grade B recommendation, which means there is "high certainty that the net benefit is moderate or there is moderate certainty that the next benefit is moderate to substantial."

However, routine use of these drugs in women who are not at increased risk for breast cancer is not recommended.

Recently, the American Society of Clinical Oncology also issued guidelines on chemoprevention for breast cancer, and recommended that tamoxifen and raloxifene "should be discussed as an option."

Also Recommended in Britain

Chemoprevention of breast cancer with tamoxifen and raloxifene is recommended for women in England and Wales who have a high risk for breast cancer in an updated guideline from the National Institute for Health and Care Excellence.

Putting the recommendations into practice is another story, however. So far, there has been little use of chemoprevention for breast cancer, with few women who could benefit from this intervention choosing to take these drugs.

Ann Intern Med. Published online September 24, 2013. Full text

Study Highlights

  • The recommendation applies to asymptomatic women 35 years or older without prior breast cancer or in situ breast cancer.
  • Women should undergo risk stratification for breast cancer, and there are several methods for assessing these risks. Risk models perform best among women older than 60 years who receive annual mammography, and they are most effective at predicting the risk for estrogen receptor–positive breast cancer.
  • A risk for incident breast cancer of 3% or more during 5 years was considered sufficiently high risk by the USPSTF to consider primary preventive medical therapy.
  • Nonetheless, most women with a high risk for breast cancer will not go on to have the disease, and most breast cancer cases do not occur among high-risk patients.
  • Both tamoxifen and raloxifene significantly reduce the risk for estrogen receptor–positive breast cancer only, with an effect of 7 to 9 fewer invasive cancers per 1000 women treated for 5 years.
  • Tamoxifen is more effective than raloxifene, reducing the relative number of invasive breast cancer events by 5 per 1000 women during 5 years of therapy.
  • Neither tamoxifen nor raloxifene is effective at reducing the risks for noninvasive breast cancer or overall mortality.
  • However, tamoxifen and raloxifene can increase the risk for venous thromboembolism by 4 to 7 events per 1000 women during 5 years. The risk for venous thromboembolism is higher with tamoxifen vs raloxifene.
  • Tamoxifen, but not raloxifene, increases the risk for endometrial cancer among women (4 more cases per 1000 women treated for 5 years).
  • Tamoxifen is associated with fewer nonvertebral fractures vs placebo, whereas raloxifene reduces the risk for vertebral fractures.
  • The usual dose of tamoxifen is 20 mg daily, and the usual dose of raloxifene is 60 mg daily. The typical treatment period is 5 years.
  • Tamoxifen is approved for breast cancer prevention among women 35 years and older. Raloxifene is indicated for postmenopausal women.
  • Overall, the USPSTF recommends that women at high risk for breast cancer participate in shared decision making regarding the use of medications to reduce their risk for this disease. These women may be treated with tamoxifen or raloxifene (B recommendation: There is high certainty that the net benefit is moderate, or there is moderate certainty that the net benefit is moderate to substantial).
  • Women with a low or average risk for breast cancer should not receive primary medical prevention therapy.

Clinical Implications

  • Breast cancer is the most common nonskin cancer among women in the United States, with a lifetime prevalence of 12.4%. The median age at the time of diagnosis of breast cancer is 61 years, and African American women are at particularly high risk for breast cancer mortality.
  • The USPSTF recommends consideration of primary preventive therapy with raloxifene or tamoxifen for women at high risk for breast cancer.

CME Test

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