Department of Biomedical Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
IEEE Trans Biomed Eng. 2010 Jul;57(7):1676-89. doi: 10.1109/TBME.2010.2041232. Epub 2010 Feb 17.
The presence of lymphocytic infiltration (LI) has been correlated with nodal metastasis and tumor recurrence in HER2+ breast cancer (BC). The ability to automatically detect and quantify extent of LI on histopathology imagery could potentially result in the development of an image based prognostic tool for human epidermal growth factor receptor-2 (HER2+) BC patients. Lymphocyte segmentation in hematoxylin and eosin (H&E) stained BC histopathology images is complicated by the similarity in appearance between lymphocyte nuclei and other structures (e.g., cancer nuclei) in the image. Additional challenges include biological variability, histological artifacts, and high prevalence of overlapping objects. Although active contours are widely employed in image segmentation, they are limited in their ability to segment overlapping objects and are sensitive to initialization. In this paper, we present a new segmentation scheme, expectation-maximization (EM) driven geodesic active contour with overlap resolution (EMaGACOR), which we apply to automatically detecting and segmenting lymphocytes on HER2+ BC histopathology images. EMaGACOR utilizes the expectation-maximization algorithm for automatically initializing a geodesic active contour (GAC) and includes a novel scheme based on heuristic splitting of contours via identification of high concavity points for resolving overlapping structures. EMaGACOR was evaluated on a total of 100 HER2+ breast biopsy histology images and was found to have a detection sensitivity of over 86% and a positive predictive value of over 64%. By comparison, the EMaGAC model (without overlap resolution) and GAC model yielded corresponding detection sensitivities of 42% and 19%, respectively. Furthermore, EMaGACOR was able to correctly resolve over 90% of overlaps between intersecting lymphocytes. Hausdorff distance (HD) and mean absolute distance (MAD) for EMaGACOR were found to be 2.1 and 0.9 pixels, respectively, and significantly better compared to the corresponding performance of the EMaGAC and GAC models. EMaGACOR is an efficient, robust, reproducible, and accurate segmentation technique that could potentially be applied to other biomedical image analysis problems.
淋巴细胞浸润 (LI) 的存在与 HER2+乳腺癌 (BC) 的淋巴结转移和肿瘤复发相关。能够自动检测和量化组织病理学图像上 LI 的程度,可能会为 HER2+BC 患者开发基于图像的预后工具。苏木精和伊红 (H&E) 染色的 BC 组织病理学图像中的淋巴细胞分割受到图像中淋巴细胞核与其他结构(例如,癌细胞核)之间外观相似性的影响。此外,还存在生物变异性、组织学伪影和高重叠物体的普遍性等挑战。尽管主动轮廓在图像分割中得到广泛应用,但它们在分割重叠物体方面的能力有限,并且对初始化很敏感。在本文中,我们提出了一种新的分割方案,即具有重叠分辨率的期望最大化 (EM) 驱动测地线主动轮廓(EMaGACOR),我们将其应用于自动检测和分割 HER2+BC 组织病理学图像上的淋巴细胞。EMaGACOR 利用期望最大化算法自动初始化测地线主动轮廓 (GAC),并包括一种基于通过识别高凹点对轮廓进行启发式拆分的新方案,用于解决重叠结构。EMaGACOR 在总共 100 张 HER2+乳腺癌活检组织学图像上进行了评估,检测灵敏度超过 86%,阳性预测值超过 64%。相比之下,EMaGAC 模型(无重叠分辨率)和 GAC 模型的相应检测灵敏度分别为 42%和 19%。此外,EMaGACOR 能够正确解析超过 90%的相交淋巴细胞之间的重叠。EMaGACOR 的 Hausdorff 距离 (HD) 和平均绝对距离 (MAD) 分别为 2.1 和 0.9 像素,与 EMaGAC 和 GAC 模型的相应性能相比,有显著提高。EMaGACOR 是一种高效、鲁棒、可重复和准确的分割技术,可能适用于其他生物医学图像分析问题。