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DOI: 10.1148/radiol.2393042007
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(Radiology 2006;239:677-685.)
© RSNA, 2006


Breast Imaging

Evaluation of a Prospective Scoring System Designed for a Multicenter Breast MR Imaging Screening Study1

Ruth M. L. Warren, MD, Deborah Thompson, PhD, Linda J. Pointon, MPhil, Rebecca Hoff, BSc, Fiona J. Gilbert, FRCR, Anwar R. Padhani, FRCR, Douglas F. Easton, PhD, Sunil R. Lakhani, MD, Martin O. Leach, PhD, Collaborators in the United Kingdom Medical Research Council Magnetic Resonance Imaging in Breast Screening (MARIBS) Study

1 From the Department of Radiology, Addenbrooke's Hospital, Cambridge, England (R.M.L.W.); Cancer Research-UK Genetic Epidemiology Unit, Cambridge, England (D.T., D.F.E.); Study Coordinating Office, Section of Magnetic Resonance, Institute of Cancer Research, Royal Marsden Hospital, Downs Rd, Sutton Surrey SM2 5PT, England (L.J.P., R.H., M.O.L.); Department of Radiology, University of Aberdeen, Aberdeen, Scotland (F.J.G.); Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Royal Marsden Hospital, London, England (S.R.L.); and Mount Vernon Hospital, Northwood, Middlesex, England (A.R.P.). The complete list of MARIBS group members and their affiliations is listed in Appendix E1 (radiology.rsnajnls.org/cgi/content/full/2393042007/DC1). Received November 25, 2004; revision requested January 27, 2005; revision received May 5; accepted June 3; final version accepted August 1. Supported by a project grant from the United Kingdom Medical Research Council. D.F.E. and D.T. supported by Cancer Research U.K. Genetic Epidemiology Unit. Address correspondence to M.O.L. (e-mail: martin{at}icr.ac.uk).

Purpose: To evaluate prospectively the accuracy of a lesion classification system designed for use in a magnetic resonance (MR) imaging high-breast-cancer-risk screening study.

Materials and Methods: All participating patients provided written informed consent. Ethics committee approval was obtained. The results of 1541 contrast material–enhanced breast MR imaging examinations were analyzed; 1441 screening examinations were performed in 638 women aged 24–51 years at high risk for breast cancer, and 100 examinations were performed in 100 women aged 23–81 years. Lesion analysis was performed in 991 breasts, which were divided into design (491 breasts) and testing (500 breasts) sets. The reference standard was histologic analysis of biopsy samples, fine-needle aspiration cytology, or minimal follow-up of 24 months. The scoring system involved the use of five features: morphology (MOR), pattern of enhancement (POE), percentage of maximal focal enhancement (PMFE), maximal signal intensity–time ratio (MITR), and pattern of contrast material washout (POCW). The system was evaluated by means of (a) assessment of interreader agreement, as expressed in {kappa} statistics, for 315 breasts in which both readers analyzed the same lesion, (b) assessment of the diagnostic accuracy of the scored components with receiver operating characteristic curve analysis, and (c) logistic regression analysis to determine which components of the scoring system were critical to the final score. A new simplified scoring system developed with the design set was applied to the testing set.

Results: There was moderate reader agreement regarding overall lesion outcome (ie, malignant, suspicious, or benign) ({kappa} = 0.58) and less agreement regarding the scored components. The area under the receiver operating characteristic curve (AUC) for the overall lesion score, 0.88, was higher than the AUC for any one component. The components MOR, POE, and POCW yielded the best overall result. PMFE and MITR did not contribute to diagnostic utility. Applying a simplified scoring system to the testing set yielded a nonsignificantly (P = .2) higher AUC than did applying the original scoring system (sensitivity, 84%; specificity, 86.0%).

Conclusion: Good diagnostic accuracy can be achieved by using simple qualitative descriptors of lesion enhancement, including POCW. In the context of screening, quantitative enhancement parameters appear to be less useful for lesion characterization.

Supplemental material: radiology.rsnajnls.org/cgi/content/full/2393042007/DC1

© RSNA, 2006




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