Brandt Kathleen R, Scott Christopher G, Ma Lin, Mahmoudzadeh Amir P, Jensen Matthew R, Whaley Dana H, Wu Fang Fang, Malkov Serghei, Hruska Carrie B, Norman Aaron D, Heine John, Shepherd John, Pankratz V Shane, Kerlikowske Karla, Vachon Celine M
From the Departments of Radiology (K.R.B., D.H.W., C.B.H.) and Health Sciences Research (C.G.S., M.R.J., F.F.W., A.D.N., C.M.V.), Mayo Clinic, 200 First St SW, Rochester, MN 55905; Department of Medicine (L.M.), Department of Radiology and Biomedical Imaging (A.P.M., J.S.), Department of Radiology (S.M.), Departments of Medicine and Epidemiology and Biostatistics, Division of General Internal Medicine, Department of Medicine (K.K.), University of California, San Francisco, San Francisco, Calif; Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center, Tampa, Fla (J.H.); and Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, NM (V.S.P.).
Radiology. 2016 Jun;279(3):710-9. doi: 10.1148/radiol.2015151261. Epub 2015 Dec 22.
Purpose To compare the classification of breast density with two automated methods, Volpara (version 1.5.0; Matakina Technology, Wellington, New Zealand) and Quantra (version 2.0; Hologic, Bedford, Mass), with clinical Breast Imaging Reporting and Data System (BI-RADS) density classifications and to examine associations of these measures with breast cancer risk. Materials and Methods In this study, 1911 patients with breast cancer and 4170 control subjects matched for age, race, examination date, and mammography machine were evaluated. Participants underwent mammography at Mayo Clinic or one of four sites within the San Francisco Mammography Registry between 2006 and 2012 and provided informed consent or a waiver for research, in compliance with HIPAA regulations and institutional review board approval. Digital mammograms were retrieved a mean of 2.1 years (range, 6 months to 6 years) before cancer diagnosis, with the corresponding clinical BI-RADS density classifications, and Volpara and Quantra density estimates were generated. Agreement was assessed with weighted κ statistics among control subjects. Breast cancer associations were evaluated with conditional logistic regression, adjusted for age and body mass index. Odds ratios, C statistics, and 95% confidence intervals (CIs) were estimated. Results Agreement between clinical BI-RADS density classifications and Volpara and Quantra BI-RADS estimates was moderate, with κ values of 0.57 (95% CI: 0.55, 0.59) and 0.46 (95% CI: 0.44, 0.47), respectively. Differences of up to 14% in dense tissue classification were found, with Volpara classifying 51% of women as having dense breasts, Quantra classifying 37%, and clinical BI-RADS assessment used to classify 43%. Clinical and automated measures showed similar breast cancer associations; odds ratios for extremely dense breasts versus scattered fibroglandular densities were 1.8 (95% CI: 1.5, 2.2), 1.9 (95% CI: 1.5, 2.5), and 2.3 (95% CI: 1.9, 2.8) for Volpara, Quantra, and BI-RADS classifications, respectively. Clinical BI-RADS assessment showed better discrimination of case status (C = 0.60; 95% CI: 0.58, 0.61) than did Volpara (C = 0.58; 95% CI: 0.56, 0.59) and Quantra (C = 0.56; 95% CI: 0.54, 0.58) BI-RADS classifications. Conclusion Automated and clinical assessments of breast density are similarly associated with breast cancer risk but differ up to 14% in the classification of women with dense breasts. This could have substantial effects on clinical practice patterns. (©) RSNA, 2015 Online supplemental material is available for this article.
目的 比较两种自动方法Volpara(1.5.0版本;Matakina Technology,惠灵顿,新西兰)和Quantra(2.0版本;Hologic,贝德福德,马萨诸塞州)对乳腺密度的分类与临床乳腺影像报告和数据系统(BI-RADS)密度分类,并研究这些测量值与乳腺癌风险的关联。材料与方法 在本研究中,对1911例乳腺癌患者和4170名年龄、种族、检查日期及乳腺X线摄影设备相匹配的对照者进行了评估。参与者于2006年至2012年期间在梅奥诊所或旧金山乳腺X线摄影登记处的四个地点之一接受了乳腺X线摄影,并根据健康保险流通与责任法案(HIPAA)规定和机构审查委员会批准,提供了知情同意书或研究豁免同意书。在癌症诊断前平均2.1年(范围6个月至6年)获取数字化乳腺X线摄影图像,同时获取相应的临床BI-RADS密度分类,并生成Volpara和Quantra密度估计值。采用加权κ统计量评估对照者之间的一致性。采用条件逻辑回归评估乳腺癌关联,对年龄和体重指数进行校正。估计比值比、C统计量和95%置信区间(CI)。结果 临床BI-RADS密度分类与Volpara和Quantra的BI-RADS估计值之间的一致性为中等,κ值分别为0.57(95%CI:0.55,0.59)和0.46(95%CI:0.44,0.47)。发现致密组织分类差异高达14%,Volpara将51%的女性分类为乳腺致密,Quantra分类为37%,临床BI-RADS评估分类为43%。临床和自动测量显示出相似的乳腺癌关联;对于Volpara、Quantra和BI-RADS分类,极度致密乳腺与散在纤维腺体型乳腺的比值比分别为1.8(95%CI:1.5,2.2)、1.9(95%CI:1.5,2.5)和2.3(95%CI:1.9,2.8)。临床BI-RADS评估对病例状态的鉴别能力(C = 0.60;95%CI:0.58, 0.61)优于Volpara(C = 0.58;95%CI:0.56, 0.59)和Quantra(C = 0.56;95%CI:0.54, 0.58)的BI-RADS分类。结论 乳腺密度的自动评估和临床评估与乳腺癌风险的关联相似,但在乳腺致密女性的分类上差异高达14%。这可能对临床实践模式产生重大影响。(©)RSNA,2015 本文提供在线补充材料。