Background:
Few studies have examined the comparative effectiveness of digital versus film-screen mammography in U.S. community practice.
Objective:
To determine whether the interpretive performance of digital and film-screen mammography differs.
Design:
Prospective cohort study.
Setting:
Mammography facilities in the Breast Cancer Surveillance Consortium.
Participants:
329 261 women aged 40 to 79 years underwent 869 286 mammograms (231 034 digital; 638 252 film-screen).
Measurements:
Invasive cancer or ductal carcinoma in situ diagnosed within 12 months of a digital or film-screen examination and calculation of mammography sensitivity, specificity, cancer detection rates, and tumor outcomes.
Results:
Overall, cancer detection rates and tumor characteristics were similar for digital and film-screen mammography, but the sensitivity and specificity of each modality varied by age, tumor characteristics, breast density, and menopausal status. Compared with film-screen mammography, the sensitivity of digital mammography was significantly higher for women aged 60 to 69 years (89.9% vs. 83.0%; P = 0.014) and those with estrogen receptor–negative cancer (78.5% vs. 65.8%; P = 0.016); borderline significantly higher for women aged 40 to 49 years (82.4% vs. 75.6%; P = 0.071), those with extremely dense breasts (83.6% vs. 68.1%; P = 0.051), and pre- or perimenopausal women (87.1% vs. 81.7%; P = 0.057); and borderline significantly lower for women aged 50 to 59 years (80.5% vs. 85.1%; P = 0.097). The specificity of digital and film-screen mammography was similar by decade of age, except for women aged 40 to 49 years (88.0% vs. 89.7%; P < 0.001).
Limitation:
Statistical power for subgroup analyses was limited.
Conclusion:
Overall, cancer detection with digital or film-screen mammography is similar in U.S. women aged 50 to 79 years undergoing screening mammography. Women aged 40 to 49 years are more likely to have extremely dense breasts and estrogen receptor–negative tumors; if they are offered mammography screening, they may choose to undergo digital mammography to optimize cancer detection.
Primary Funding Source:
National Cancer Institute.
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Author, Article and Disclosure Information
From University of California, San Francisco, and San Francisco Veterans Affairs Medical Center, San Francisco, California; Group Health Research Institute, Group Health Cooperative, University of Washington School of Public Health and Community Medicine, and University of Washington School of Medicine, Seattle, Washington; Health Promotion Research, University of Vermont, College of Medicine, Burlington, Vermont; University of North Carolina at Chapel Hill, Chapel Hill, North Carolina;
and Applied Research Program, National Cancer Institute, Rockville, Maryland.
Acknowledgment: The authors thank the participating women, mammography facilities, and radiologists for the data they have provided for this study. A list of BCSC investigators and procedures for requesting BCSC data for research purposes can be found at breastscreening.cancer.gov/.
Grant Support: By the National Cancer Institute–funded BCSC cooperative agreement (grants U01CA63740, U01CA86076, U01CA86082, U01CA63736, U01CA70013, U01CA69976, U01CA63731, and U01CA70040) and National Cancer Institute grants R03CA150007 and RC2CA148577. The collection of cancer data used in this study was supported in part by several state public health departments and cancer registries throughout the United States; for a full description of these sources, see breastscreening.cancer.gov/work/acknowledgement.html.
Disclosures: Disclosures can be viewed at www.acponline.org/authors/icmje/ConflictOfInterestForms.do?msNum=M10-2769.
Reproducible Research Statement:Study protocol: Available from Dr. Kerlikowske (e-mail, Karla.
Corresponding Author: Karla Kerlikowske, MD, San Francisco Veterans Affairs Medical Center, General Internal Medicine Section, 111A1, 4150 Clement Street, San Francisco, CA 94121; e-mail, Karla.
Current Author Addresses: Dr. Kerlikowske: San Francisco Veterans Affairs Medical Center, General Internal Medicine Section, 111A1, 4150 Clement Street, San Francisco, CA 94121.
Drs. Hubbard and Miglioretti: Group Health Research Institute, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101-1448.
Dr. Geller: Health Promotion Research, University of Vermont, 429AR4, One South Prospect Street, Elevator C-4426, Burlington, VT 05401-3444.
Dr. Yankaskas: Department of Radiology, CB #7515, MRI, University of North Carolina, 106 Mason Farm Road, Chapel Hill, NC 27599-7515.
Dr. Lehman: Seattle Cancer Care Alliance, 825 Eastlake Avenue East, G2-600, Seattle, WA 98109.
Dr. Taplin: National Cancer Institute, 6130 Executive Boulevard, Rockville, MD 20852-7344.
Dr. Sickles: Department of Radiology, Box 1667, UCSF Medical Center, San Francisco, CA 94143-1667.
Author Contributions: Conception and design: K. Kerlikowske, R.A. Hubbard, D.L. Miglioretti, B.M. Geller, B.C. Yankaskas, S. Taplin.
Analysis and interpretation of the data: K. Kerlikowske, R.A. Hubbard, D.L. Miglioretti, B.M. Geller, B.C. Yankaskas, E.A. Sickles.
Drafting of the article: K. Kerlikowske, R.A. Hubbard, B.M. Geller, B.C. Yankaskas, C.D. Lehman, S. Taplin.
Critical revision of the article for important intellectual content: K. Kerlikowske, R.A. Hubbard, B.M. Geller, B.C. Yankaskas, C.D. Lehman, S. Taplin, E.A. Sickles.
Final approval of the article: K. Kerlikowske, R.A. Hubbard, D.L. Miglioretti, B.M. Geller, B.C. Yankaskas, C.D. Lehman, S. Taplin, E.A. Sickles.
Statistical expertise: R.A. Hubbard, D.L. Miglioretti.
Obtaining of funding: K. Kerlikowske, D.L. Miglioretti, B.C. Yankaskas, S. Taplin.
Collection and assembly of data: K. Kerlikowske, R.A. Hubbard, D.L. Miglioretti, B.M. Geller, B.C. Yankaskas.

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