Medication Use to Reduce Risk of Breast Cancer US Preventive Services Task Force Recommendation Statement

被引:137
作者
Owens, Douglas K. [1 ,2 ]
Davidson, Karina W. [3 ]
Krist, Alex H. [4 ,5 ]
Barry, Michael J. [6 ]
Cabana, Michael [7 ]
Caughey, Aaron B. [8 ]
Doubeni, Chyke A. [9 ]
Epling, John W., Jr. [10 ]
Kubik, Martha [11 ]
Landefeld, C. Seth [12 ]
Mangione, Carol M. [13 ]
Pbert, Lori [14 ]
Silverstein, Michael [15 ]
Tseng, Chien-Wen [16 ,17 ]
Wong, John B. [18 ]
机构
[1] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
[2] Stanford Univ, 616 Serra St,Encina Hall,Room C336, Stanford, CA 94305 USA
[3] Northwell Hlth, Feinstein Inst Med Res, Manhasset, NY USA
[4] Fairfax Family Practice Residency, Fairfax, VA USA
[5] Virginia Commonwealth Univ, Richmond, VA USA
[6] Harvard Med Sch, Boston, MA 02115 USA
[7] Univ Calif San Francisco, San Francisco, CA 94143 USA
[8] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[9] Mayo Clin, Rochester, NY USA
[10] Virginia Tech Carilion Sch Med, Roanoke, VA USA
[11] Temple Univ, Philadelphia, PA 19122 USA
[12] Univ Alabama Birmingham, Birmingham, AL USA
[13] Univ Calif Los Angeles, Los Angeles, CA USA
[14] Univ Massachusetts, Med Sch, Worcester, MA 01605 USA
[15] Boston Univ, Boston, MA 02215 USA
[16] Univ Hawaii, Honolulu, HI 96822 USA
[17] Pacific Hlth Res & Educ Inst, Honolulu, HI USA
[18] Tufts Univ, Sch Med, Boston, MA 02111 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2019年 / 322卷 / 09期
基金
美国医疗保健研究与质量局;
关键词
SURGICAL ADJUVANT BREAST; ITALIAN RANDOMIZED-TRIAL; VERTEBRAL FRACTURE RISK; QUALITY-OF-LIFE; POSTMENOPAUSAL WOMEN; MULTIPLE OUTCOMES; CARDIOVASCULAR EVENTS; RALOXIFENE EVALUATION; PREDICTION MODEL; BOWEL PROJECT;
D O I
10.1001/jama.2019.11885
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Breast cancer is the most common nonskin cancer among women in the United States and the second leading cause of cancer death. The median age at diagnosis is 62 years, and an estimated 1 in 8 women will develop breast cancer at some point in their lifetime. African American women are more likely to die of breast cancer compared with women of other races. OBJECTIVE To update the 2013 US Preventive Services Task Force (USPSTF) recommendation on medications for risk reduction of primary breast cancer. EVIDENCE REVIEW The USPSTF reviewed evidence on the accuracy of risk assessment methods to identify women who could benefit from risk-reducing medications for breast cancer, as well as evidence on the effectiveness, adverse effects, and subgroup variations of these medications. The USPSTF reviewed evidence from randomized trials, observational studies, and diagnostic accuracy studies of risk stratification models in women without preexisting breast cancer or ductal carcinoma in situ. FINDINGS The USPSTF found convincing evidence that risk assessment tools can predict the number of cases of breast cancer expected to develop in a population. However, these risk assessment tools perform modestly at best in discriminating between individual women who will or will not develop breast cancer. The USPSTF found convincing evidence that risk-reducing medications (tamoxifen, raloxifene, or aromatase inhibitors) provide at least a moderate benefit in reducing risk for invasive estrogen receptor-positive breast cancer in postmenopausal women at increased risk for breast cancer. The USPSTF found that the benefits of taking tamoxifen, raloxifene, and aromatase inhibitors to reduce risk for breast cancer are no greater than small in women not at increased risk for the disease. The USPSTF found convincing evidence that tamoxifen and raloxifene and adequate evidence that aromatase inhibitors are associated with small to moderate harms. Overall, the USPSTF determined that the net benefit of taking medications to reduce risk of breast cancer is larger in women who have a greater risk for developing breast cancer. CONCLUSIONS AND RECOMMENDATION The USPSTF recommends that clinicians offer to prescribe risk-reducing medications, such as tamoxifen, raloxifene, or aromatase inhibitors, to women who are at increased risk for breast cancer and at low risk for adverse medication effects. (B recommendation) The USPSTF recommends against the routine use of risk-reducing medications, such as tamoxifen, raloxifene, or aromatase inhibitors, in women who are not at increased risk for breast cancer. (D recommendation) This recommendation applies to asymptomatic women 35 years and older, including women with previous benign breast lesions on biopsy (such as atypical ductal or lobular hyperplasia and lobular carcinoma in situ). This recommendation does not apply to women who have a current or previous diagnosis of breast cancer or ductal carcinoma in situ.
引用
收藏
页码:857 / 867
页数:11
相关论文
共 94 条
[1]  
Adams-Campbell LL, 2007, BREAST J, V13, P332, DOI 10.1111/j.1524-4741.2007.00439.x
[2]  
American Academy of Family Physicians (AAFP), CLIN PREV SERV REC M
[3]   Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programme [J].
Amir, E ;
Evans, DG ;
Shenton, A ;
Lalloo, F ;
Moran, A ;
Boggis, C ;
Wilson, M ;
Howell, A .
JOURNAL OF MEDICAL GENETICS, 2003, 40 (11) :807-814
[4]  
[Anonymous], 2014, Obstet Gynecol, V123, P1394, DOI 10.1097/01.AOG.0000450757.18294.cf
[5]  
[Anonymous], 2017, Obstet Gynecol, V130, pe110, DOI 10.1097/AOG.0000000000002296
[6]  
[Anonymous], 2017, Breast cancer facts and figures 2017-2018
[7]  
[Anonymous], 2018, CANC FACTS FIG 2018
[8]  
[Anonymous], 2021, PLYMOUTH M
[9]   Prescription of tamoxifen for breast cancer prevention by primary care physicians [J].
Armstrong, Katrina ;
Quistberg, D. Alex ;
Micco, Ellyn ;
Domchek, Susan ;
Guerra, Carmen .
ARCHIVES OF INTERNAL MEDICINE, 2006, 166 (20) :2260-2265
[10]   Prospective breast cancer risk prediction model for women undergoing screening mammography [J].
Barlow, William E. ;
White, Emily ;
Ballard-Barbash, Rachel ;
Vacek, Pamela M. ;
Titus-Ernstoff, Linda ;
Carney, Patricia A. ;
Tice, Jeffrey A. ;
Buist, Diana S. M. ;
Geller, Berta M. ;
Rosenberg, Robert ;
Yankaskas, Bonnie C. ;
Kerlikowske, Karla .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (17) :1204-1214