George R Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2013 Jan 8;110(2):471-6. doi: 10.1073/pnas.1215473110. Epub 2012 Dec 24.
Microcalcifications geographically target the location of abnormalities within the breast and are of critical importance in breast cancer diagnosis. However, despite stereotactic guidance, core needle biopsy fails to retrieve microcalcifications in up to 15% of patients. Here, we introduce an approach based on diffuse reflectance spectroscopy for detection of microcalcifications that focuses on variations in optical absorption stemming from the calcified clusters and the associated cross-linking molecules. In this study, diffuse reflectance spectra are acquired ex vivo from 203 sites in fresh biopsy tissue cores from 23 patients undergoing stereotactic breast needle biopsies. By correlating the spectra with the corresponding radiographic and histologic assessment, we have developed a support vector machine-derived decision algorithm, which shows high diagnostic power (positive predictive value and negative predictive value of 97% and 88%, respectively) for diagnosis of lesions with microcalcifications. We further show that these results are robust and not due to any spurious correlations. We attribute our findings to the presence of proteins (such as elastin), and desmosine and isodesmosine cross-linkers in the microcalcifications. It is important to note that the performance of the diffuse reflectance decision algorithm is comparable to one derived from the corresponding Raman spectra, and the considerably higher intensity of the reflectance signal enables the detection of the targeted lesions in a fraction of the spectral acquisition time. Our findings create a unique landscape for spectroscopic validation of breast core needle biopsy for detection of microcalcifications that can substantially improve the likelihood of an adequate, diagnostic biopsy in the first attempt.
微钙化在空间上定位乳房内的异常位置,对乳腺癌的诊断至关重要。然而,尽管采用了立体定向引导,核心针活检仍未能在多达 15%的患者中获取微钙化。在这里,我们介绍了一种基于漫反射光谱的方法,用于检测微钙化,该方法侧重于源于钙化簇和相关交联分子的光吸收变化。在这项研究中,从 23 名接受立体定向乳房针活检的患者的新鲜活检组织芯的 203 个部位获取了漫反射光谱。通过将光谱与相应的放射学和组织学评估相关联,我们开发了一种基于支持向量机的决策算法,该算法对诊断具有微钙化的病变具有很高的诊断能力(阳性预测值和阴性预测值分别为 97%和 88%)。我们进一步表明,这些结果是稳健的,并非由于任何虚假关联。我们将我们的发现归因于微钙化中存在的蛋白质(如弹性蛋白)以及交联分子中的desmosine 和 isodesmosine。值得注意的是,漫反射决策算法的性能可与源自相应拉曼光谱的算法相媲美,并且反射信号的强度要高得多,这使得在光谱采集时间的一小部分内就可以检测到目标病变。我们的研究结果为通过光谱学验证乳腺核心针活检来检测微钙化提供了独特的依据,这可以极大地提高首次尝试进行充分诊断性活检的可能性。