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Spots Global Cancer Trial Database for Digital Mammography Screening Trial (ACRIN6652)

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Trial Identification

Brief Title: Digital Mammography Screening Trial (ACRIN6652)

Official Title: Screening and Diagnostic Trial to Compare the Effectiveness of Two Types of Mammography in Detecting Breast Cancer in Women

Study ID: NCT00008346

Conditions

Breast Cancer

Study Description

Brief Summary: RATIONALE: Screening tests may help doctors detect cancer cells early and plan more effective treatment for cancer. It is not yet known which type of mammography is more effective in detecting breast cancer. PURPOSE: Screening and diagnostic trial to compare the effectiveness of two types of mammography in detecting breast cancer in women.

Detailed Description: OBJECTIVES: * Compare the diagnostic performance of digital mammography vs screen-film mammography, as measured by the area under the Receiver Operating Characteristic (ROC) curve, sensitivity, specificity, and positive and negative predictive values, in the detection of breast cancer in women. * Compare the diagnostic accuracy of the digital mammogram obtained using each of the individual manufacturer's digital units vs screen-film mammography through retrospective reader studies. * Determine the effects of patient characteristics, including age, lesion type, pathologic diagnosis, menopausal and hormonal status, breast density, and family history, on diagnostic accuracy of digital mammography. * Determine the effects of technical parameters, including display type, machine type, and detector spatial and contrast resolution, on diagnostic accuracy of digital mammography. * Determine the effect of reduced false-positive mammograms that are expected with digital mammography on the health-related quality of life and personal anxiety of women undergoing this screening experience. * Compare the diagnostic performance of digital mammography with the rate of cancer in a set of cases through a retrospective reader study. * Compare the effect of softcopy vs printed film display on the diagnostic performance of digital mammography through a retrospective reader study. * Compare the effect of breast density on the diagnostic accuracy of digital mammography vs screen-film mammography through a retrospective reader study. * Compare the image quality and breast radiation dose in digital vs screen-film mammography in these participants. * Determine the temporal variations in image quality, breast radiation dose, and other quality control parameters in the participating study centers. OUTLINE: This is a randomized, multicenter study. Participants with postitive screening results are stratified according to age (under 50 vs 50-59 vs 60-70 vs over 70). Participants are randomized to one of two treatment arms. * Arm I: Participants undergo a two-view screen-film mammogram followed by a two-view digital mammogram of each breast. * Arm II: Participants undergo a two-view digital mammogram followed by a two-view screen-film mammogram of each breast. Quality of life is assessed before the screening mammogram in the first 800 women enrolled. In an additional 1,200 participants (600 with positive screening results and 600 with negative screening results), quality of life is assessed shortly after the screening mammogram and at 1 year. Participants are followed at 1 year with a repeat screen-film or digital mammogram. PROJECTED ACCRUAL: A total of 49,500 participants (24,750 per arm) will be accrued for this study within 18 months.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California, United States

University of California Davis Cancer Center, Sacramento, California, United States

University of Colorado Cancer Center at University of Colorado Health Sciences Center, Aurora, Colorado, United States

Washington Radiology Associates, P.C., Washington, D.C., District of Columbia, United States

H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, United States

Emory Health Care Clinic, Atlanta, Georgia, United States

Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, United States

University of Chicago Cancer Research Center, Chicago, Illinois, United States

La Grange Memorial Hospital, La Grange, Illinois, United States

Holden Comprehensive Cancer Center at University of Iowa, Iowa City, Iowa, United States

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, United States

Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Lahey Clinic - Burlington, Burlington, Massachusetts, United States

William Beaumont Hospital, Royal Oak, Michigan, United States

Siteman Cancer Center, Saint Louis, Missouri, United States

Monmouth Medical Center, Long Branch, New Jersey, United States

Shore Memorial Hospital, Somers Point, New Jersey, United States

Memorial Sloan-Kettering Cancer Center, New York, New York, United States

Mount Sinai School of Medicine, New York, New York, United States

Herbert Irving Comprehensive Cancer Center at Columbia University, New York, New York, United States

Elizabeth Wende Breast Clinic, Rochester, New York, United States

Lineberger Comprehensive Cancer Center, UNC, Chapel Hill, North Carolina, United States

Charles M. Barrett Cancer Center at University Hospital, Cincinnati, Ohio, United States

Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania, United States

Kimmel Cancer Center of Thomas Jefferson University - Philadelphia, Philadelphia, Pennsylvania, United States

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States

Roger Williams Medical Center/BUSM, Providence, Rhode Island, United States

Simmons Cancer Center - Dallas, Dallas, Texas, United States

Cancer Center at the University of Virginia, Charlottesville, Virginia, United States

University of Washington Medical Center, Seattle, Washington, United States

Sunnybrook and Women's College Health Sciences Centre, North York, Ontario, Canada

Contact Details

Name: Etta Pisano, MD

Affiliation: UNC Lineberger Comprehensive Cancer Center

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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