Manchester Institute of Biotechnology, University of Manchester , 131 Princess Street, Manchester M1 7DN, U.K.
Anal Chem. 2017 Jul 18;89(14):7348-7355. doi: 10.1021/acs.analchem.7b00426. Epub 2017 Jul 3.
Fourier transform infrared (FT-IR) microscopy coupled with machine learning approaches has been demonstrated to be a powerful technique for identifying abnormalities in human tissue. The ability to objectively identify the prediseased state and diagnose cancer with high levels of accuracy has the potential to revolutionize current histopathological practice. Despite recent technological advances in FT-IR microscopy, sample throughput and speed of acquisition are key barriers to clinical translation. Wide-field quantum cascade laser (QCL) infrared imaging systems with large focal plane array detectors utilizing discrete frequency imaging have demonstrated that large tissue microarrays (TMA) can be imaged in a matter of minutes. However, this ground breaking technology is still in its infancy, and its applicability for routine disease diagnosis is, as yet, unproven. In light of this, we report on a large study utilizing a breast cancer TMA comprised of 207 different patients. We show that by using QCL imaging with continuous spectra acquired between 912 and 1800 cm, we can accurately differentiate between 4 different histological classes. We demonstrate that we can discriminate between malignant and nonmalignant stroma spectra with high sensitivity (93.56%) and specificity (85.64%) for an independent test set. Finally, we classify each core in the TMA and achieve high diagnostic accuracy on a patient basis with 100% sensitivity and 86.67% specificity. The absence of false negatives reported here opens up the possibility of utilizing high throughput chemical imaging for cancer screening, thereby reducing pathologist workload and improving patient care.
傅里叶变换红外(FT-IR)显微镜结合机器学习方法已被证明是一种强大的技术,可用于识别人体组织中的异常。能够客观地识别疾病前期状态并以高精度诊断癌症,有可能彻底改变当前的组织病理学实践。尽管 FT-IR 显微镜技术最近取得了进展,但样本通量和采集速度仍然是临床转化的关键障碍。具有大焦平面阵列探测器的宽场量子级联激光器(QCL)红外成像系统利用离散频率成像,已经证明可以在几分钟内对大型组织微阵列(TMA)进行成像。然而,这项开创性技术仍处于起步阶段,其在常规疾病诊断中的适用性尚未得到证实。有鉴于此,我们报告了一项利用包含 207 名不同患者的乳腺癌 TMA 的大型研究。我们表明,通过使用 QCL 成像,在 912 到 1800 cm 之间连续采集光谱,我们可以准确地区分 4 种不同的组织学类型。我们证明,我们可以以 93.56%的高灵敏度和 85.64%的特异性区分恶性和非恶性基质光谱,对于独立测试集也是如此。最后,我们对 TMA 中的每个核心进行分类,并以患者为基础实现了高诊断准确性,灵敏度为 100%,特异性为 86.67%。这里报告的没有假阴性的情况为利用高通量化学成像进行癌症筛查开辟了可能性,从而减少病理学家的工作量并改善患者护理。