reast cancer is the second leading cause of cancer-related deaths and the most commonly diagnosed cancer in women across the world (1). Digital mammography (DM) is the primary imaging modality of breast cancer screening in women who are asymptomatic. In a diagnostic workup setting (2), DM has been shown to reduce breast cancer mortality (3). In standard clinical practice, a radiologist reads mammograms and classifies the findings according to the American College of Radiology (4) Breast Imaging Reporting and Data System (BI-RADS) lexicon. An abnormal finding depicted at DM typically requires a diagnostic workup, which may include additional mammographic views or possibly additional imaging modalities. If a lesion is suspicious for cancer, further evaluation with a biopsy is recommended. Analyzing these images is challenging because of the subtle differences between lesions and background fibroglandular tissue, different lesion types, the nonrigid nature of the breast, and the relatively small proportion of cancers in a screening population of women at average risk (2). This leads to substantial intraobserver and interobserver variability (5). The average performance measures for screening mammography by a radiologist was reported by Lehman et al (6) to be 86.9% sensitivity and 88.9% specificity. Breast cancer risk prediction models on the basis of clinical features can help physicians estimate the probability of an individual or population to develop breast cancer within certain time frames. As a result, they are often used to recommend an individual screening plan. In a systematic survey of risk prediction models, Meads et al (7) reported a limited performance when applied to general populations (area under the receiver operating characteristic curve [AUC], 0.67; 95% confidence interval [CI]: 0.65, 0.68), and showed improved results when applied to high-risk populations (AUC, 0.76; 95% CI: 0.70, 0.82).