Department of Radiation Oncology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Institute of Diagnostic and Interventional Radiology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Br J Radiol. 2021 Apr 1;94(1120):20200947. doi: 10.1259/bjr.20200947. Epub 2021 Feb 5.
In this study, we aimed to assess the impact of different CT reconstruction kernels on the stability of radiomic features and the transferability between different diseases and tissue types. Three lung diseases were evaluated, . non-small cell lung cancer (NSCLC), malignant pleural mesothelioma (MPM) and interstitial lung disease related to systemic sclerosis (SSc-ILD) as well as four different tissue types, . primary tumor, largest involved lymph node ipsilateral and contralateral lung.
Pre-treatment non-contrast enhanced CT scans from 23 NSCLC, 10 MPM and 12 SSc-ILD patients were collected retrospectively. For each patient, CT scans were reconstructed using smooth and sharp kernel in filtered back projection. The regions of interest (ROIs) were contoured on the smooth kernel-based CT and transferred to the sharp kernel-based CT. The voxels were resized to the largest voxel dimension of each cohort. In total, 1386 features were analyzed. Feature stability was assessed using the intraclass correlation coefficient. Features above the stability threshold >0.9 were considered stable.
We observed a strong impact of the reconstruction method on stability of the features (at maximum 26% of the 1386 features were stable). Intensity features were the most stable followed by texture and wavelet features. The wavelet features showed a positive correlation between percentage of stable features and size of the ROI (R2 = 0.79, = 0.005). Lymph node radiomics showed poorest stability (<10%) and lung radiomics the largest stability (26%). Robustness analysis done on the contralateral lung could to a large extent be transferred to the ipsilateral lung, and the overlap of stable lung features between different lung diseases was more than 50%. However, results of robustness studies cannot be transferred between tissue types, which was investigated in NSCLC and MPM patients; the overlap of stable features for lymph node and lung, as well as for primary tumor and lymph node was very small in both disease types.
The robustness of radiomic features is strongly affected by different reconstruction kernels. The effect is largely influenced by the tissue type and less by the disease type.
The study presents to our knowledge the most complete analysis on the impact of convolution kernel on the robustness of CT-based radiomics for four relevant tissue types in three different lung diseases. .
本研究旨在评估不同 CT 重建核对放射组学特征稳定性以及不同疾病和组织类型间可转移性的影响。我们评估了三种肺部疾病,. 非小细胞肺癌(NSCLC)、恶性胸膜间皮瘤(MPM)和系统性硬化症相关间质性肺病(SSc-ILD),以及四种不同的组织类型,. 原发肿瘤、同侧和对侧最大受累淋巴结肺。
回顾性收集了 23 例 NSCLC、10 例 MPM 和 12 例 SSc-ILD 患者的治疗前非增强 CT 扫描。对于每位患者,使用平滑核和锐化核在滤波反投影中进行 CT 重建。在平滑核 CT 上勾画感兴趣区(ROI),并转移到锐化核 CT 上。将体素调整为每个队列的最大体素维度。总共分析了 1386 个特征。使用组内相关系数评估特征稳定性。稳定性阈值 >0.9 的特征被认为是稳定的。
我们观察到重建方法对特征稳定性有强烈影响(在 1386 个特征中,最多有 26%的特征是稳定的)。强度特征是最稳定的,其次是纹理和小波特征。小波特征的稳定特征百分比与 ROI 大小之间呈正相关(R2 = 0.79, = 0.005)。淋巴结放射组学的稳定性最差(<10%),而肺放射组学的稳定性最大(26%)。对侧肺进行稳健性分析在很大程度上可以转移到同侧肺,不同肺部疾病之间稳定的肺特征重叠超过 50%。然而,两种疾病类型的淋巴结和肺、原发肿瘤和淋巴结之间的稳定特征的重叠非常小,这表明组织类型之间的稳健性研究结果无法转移。
放射组学特征的稳健性受到不同重建核的强烈影响。这种影响主要受组织类型的影响,而受疾病类型的影响较小。
本研究是迄今为止对四种与三种不同肺部疾病相关的重要组织类型的卷积核对基于 CT 的放射组学稳健性影响的最全面分析。