Collaborative Modeling of the Benefits and Harms Associated With Different US Breast Cancer Screening Strategies

被引:207
|
作者
Mandelblatt, Jeanne S. [1 ]
Stout, Natasha K. [2 ,3 ]
Schechter, Clyde B. [4 ]
van den Broek, Jeroen J. [5 ]
Miglioretti, Diana L. [6 ]
Krapcho, Martin [7 ]
Trentham-Dietz, Amy [8 ]
Munoz, Diego [9 ]
Lee, Sandra J. [10 ]
Berry, Donald A. [11 ]
van Ravesteyn, Nicolien T. [5 ]
Alagoz, Oguzhan [12 ]
Kerlikowske, Karla [13 ]
Tosteson, Anna N. A. [14 ]
Near, Aimee M. [15 ]
Hoeffken, Amanda
Chang, Yaojen [15 ]
Heijnsdijk, Eveline A. [5 ]
Chisholm, Gary [16 ]
Huang, Xuelin [17 ]
Huang, Hui [18 ]
Ergun, Mehmet Ali [19 ]
Gangnon, Ronald [20 ]
Sprague, Brian L. [21 ]
Plevritis, Sylvia [22 ]
Feuer, Eric [23 ]
de Koning, Harry J. [5 ]
Cronin, Kathleen A. [23 ]
机构
[1] Lombardi Comprehens Canc Ctr, 3300 Whitehaven St,NW,Suite 4100, Washington, DC 20007 USA
[2] Harvard Univ, Sch Med, Dept Populat Med, 133 Brookline Ave,6th Floor, Boston, MA 02215 USA
[3] Harvard Pilgrim Hlth Care Inst, 133 Brookline Ave,6th Floor, Boston, MA 02215 USA
[4] Albert Einstein Coll Med, Dept Family & Social Med, 1300 Morris Pk Ave,Black Bldg 406, Bronx, NY 10461 USA
[5] Univ Med Ctr Rotterdam, Erasmus MC, POB 2040, NL-3000 CA Rotterdam, Netherlands
[6] Univ Calif Davis, Sch Med, Dept Publ Hlth Sci, One Shields Ave,Med Sci 1C,Room 145, Davis, CA 95616 USA
[7] Information Management Serv Inc, 3901 Calverton Blvd,Suite 200, Calverton, MD 20705 USA
[8] Univ Wisconsin, Carbone Canc Ctr, 610 Walnut St,WARE Room 307, Madison, WI 53726 USA
[9] Stanford Univ, 318 Campus Dr,Room S255, Stanford, CA 94305 USA
[10] Harvard Univ, Sch Med, Dana Farber Canc Inst, Mailstop CLS11007,450 Brookline Ave, Boston, MA 02215 USA
[11] Univ Texas MD Anderson Canc Ctr, Dept Biostat, 1400 Pressler St,4-5062 Pickens Acad Tower, Houston, TX 77030 USA
[12] Univ Wisconsin, 1513 Univ Ave, Madison, WI 53706 USA
[13] Vet Affairs Med Ctr 111A1, 4150 Clement St, San Francisco, CA 94121 USA
[14] Geisel Sch Med Dartmouth, One Med Ctr Dr HB7505, Lebanon, NH 03756 USA
[15] Georgetown Univ, Lombardi Comprehens Canc Ctr, 3300 Whitehaven St NW,Suite 4100, Washington, DC 20007 USA
[16] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol & Reprod Med, Unit 1362,POB 301439, Houston, TX 77230 USA
[17] Univ Texas MD Anderson Canc Ctr, 1400 Pressler St,Unit 1411,POB 301402, Houston, TX 77230 USA
[18] Dana Farber Canc Inst, Dept Biostat & Computat Biol, 450 Brookline Ave, Boston, MA 02215 USA
[19] Univ Wisconsin, 3233 Mech Engn Bldg,1513 Univ Ave, Madison, WI 53706 USA
[20] Univ Wisconsin, Dept Populat Hlth Sci, 610 Walnut St, Madison, WI 53726 USA
[21] Univ Vermont, Off Hlth Promot Res, 1 South Prospect St, Burlington, VT 05401 USA
[22] Stanford Univ, James H Clark Ctr, Dept Radiol, Room S255,MC 5442,318 Campus Dr, Stanford, CA 94305 USA
[23] NCI, Div Canc Control & Populat Sci, 9609 Med Ctr Dr,MSC 9765,Room 4E534, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
AGE; 40; YEARS; COST-EFFECTIVENESS; UNITED-STATES; COMMUNITY PRACTICE; MENOPAUSAL STATUS; FOLLOW-UP; MAMMOGRAPHY; MORTALITY; RISK; POPULATION;
D O I
10.7326/M15-1536
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Controversy persists about optimal mammography screening strategies. Objective: To evaluate screening outcomes, taking into account advances in mammography and treatment of breast cancer. Design: Collaboration of 6 simulation models using national data on incidence, digital mammography performance, treatment effects, and other-cause mortality. Setting: United States. Patients: Average-risk U.S. female population and subgroups with varying risk, breast density, or comorbidity. Intervention: Eight strategies differing by age at which screening starts (40, 45, or 50 years) and screening interval (annual, biennial, and hybrid [annual for women in their 40s and biennial thereafter]). All strategies assumed 100% adherence and stopped at age 74 years. Measurements: Benefits (breast cancer-specific mortality reduction, breast cancer deaths averted, life-years, and quality adjusted life-years); number of mammograms used; harms (false-positive results, benign biopsies, and overdiagnosis); and ratios of harms (or use) and benefits (efficiency) per 1000 screens. Results: Biennial strategies were consistently the most efficient for average-risk women. Biennial screening from age 50 to 74 years avoided a median of 7 breast cancer deaths versus no screening; annual screening from age 40 to 74 years avoided an additional 3 deaths, but yielded 1988 more false-positive results and 11 more overdiagnoses per 1000 women screened. Annual screening from age 50 to 74 years was inefficient (similar benefits, but more harms than other strategies). For groups with a 2 to 4-fold increased risk, annual screening from age 40 years had similar harms and benefits as screening average-risk women biennially from 50 to 74 years. For groups with moderate or severe comorbidity, screening could stop at age 66 to 68 years. Limitation: Other imaging technologies, polygenic risk, and nonadherence were not considered. Conclusion: Biennial screening for breast cancer is efficient for average-risk populations. Decisions about starting ages and intervals will depend on population characteristics and the decision makers' weight given to the harms and benefits of screening.
引用
收藏
页码:215 / +
页数:16
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