Department of Electrical Engineering, Stanford University, Stanford, CA 94305, USA.
Med Phys. 2011 Nov;38(11):5879-86. doi: 10.1118/1.3643027.
It is challenging to reproducibly measure and compare cancer lesions on numerous follow-up studies; the process is time-consuming and error-prone. In this paper, we show a method to automatically and reproducibly identify and segment abnormal lymph nodes in serial computed tomography (CT) exams.
Our method leverages initial identification of enlarged (abnormal) lymph nodes in the baseline scan. We then identify an approximate region for the node in the follow-up scans using nonrigid image registration. The baseline scan is also used to locate regions of normal, non-nodal tissue surrounding the lymph node and to map them onto the follow-up scans, in order to reduce the search space to locate the lymph node on the follow-up scans. Adaptive region-growing and clustering algorithms are then used to obtain the final contours for segmentation. We applied our method to 24 distinct enlarged lymph nodes at multiple time points from 14 patients. The scan at the earlier time point was used as the baseline scan to be used in evaluating the follow-up scan, resulting in 70 total test cases (e.g., a series of scans obtained at 4 time points results in 3 test cases). For each of the 70 cases, a "reference standard" was obtained by manual segmentation by a radiologist. Assessment according to response evaluation criteria in solid tumors (RECIST) using our method agreed with RECIST assessments made using the reference standard segmentations in all test cases, and by calculating node overlap ratio and Hausdorff distance between the computer and radiologist-generated contours.
Compared to the reference standard, our method made the correct RECIST assessment for all 70 cases. The average overlap ratio was 80.7 ± 9.7% s.d., and the average Hausdorff distance was 3.2 ± 1.8 mm s.d. The concordance correlation between automated and manual segmentations was 0.978 (95% confidence interval 0.962, 0.984). The 100% agreement in our sample between our method and the standard with regard to RECIST classification suggests that the true disagreement rate is no more than 6%.
Our automated lymph node segmentation method achieves excellent overall segmentation performance and provides equivalent RECIST assessment. It potentially will be useful to streamline and improve cancer lesion measurement and tracking and to improve assessment of cancer treatment response.
在多项随访研究中,重复测量和比较癌症病变具有挑战性;这个过程既耗时又容易出错。在本文中,我们展示了一种自动且可重复地识别和分割连续计算机断层扫描(CT)检查中异常淋巴结的方法。
我们的方法利用基线扫描中对增大(异常)淋巴结的初步识别。然后,我们使用非刚性图像配准在随访扫描中识别淋巴结的大致区域。基线扫描还用于定位淋巴结周围正常的非淋巴结组织区域,并将其映射到随访扫描上,以便在随访扫描上定位淋巴结时缩小搜索空间。然后使用自适应区域生长和聚类算法获得分割的最终轮廓。我们将该方法应用于 14 名患者的 24 个不同时间点的肿大淋巴结。较早时间点的扫描用作基线扫描,用于评估随访扫描,总共产生了 70 个测试病例(例如,在 4 个时间点获得的一系列扫描产生 3 个测试病例)。对于每个 70 个病例,由放射科医生手动分割获得“参考标准”。使用我们的方法根据实体瘤反应评估标准(RECIST)进行的评估与使用参考标准分割进行的评估在所有测试病例中均一致,通过计算计算机和放射科医生生成轮廓之间的节点重叠比和 Hausdorff 距离来进行评估。
与参考标准相比,我们的方法在所有 70 个病例中均做出了正确的 RECIST 评估。平均重叠比为 80.7 ± 9.7%标准差,平均 Hausdorff 距离为 3.2 ± 1.8 毫米标准差。自动和手动分割之间的一致性相关系数为 0.978(95%置信区间 0.962,0.984)。我们的方法与标准在 RECIST 分类方面的 100%一致性表明,真实的不一致率不超过 6%。
我们的自动淋巴结分割方法实现了出色的整体分割性能,并提供了等效的 RECIST 评估。它有可能用于简化和改进癌症病变的测量和跟踪,并提高癌症治疗反应的评估。