Baid Ujjwal, Talbar Sanjay, Rane Swapnil, Gupta Sudeep, Thakur Meenakshi H, Moiyadi Aliasgar, Sable Nilesh, Akolkar Mayuresh, Mahajan Abhishek
Department of Electronics and Telecommunication Engineering, Shri Guru Gobind Singhji Institute of Engineering and Technology, Nanded, India.
Department of Pathology, Tata Memorial Centre, Tata Memorial Hospital, Mumbai, India.
Front Comput Neurosci. 2020 Feb 18;14:10. doi: 10.3389/fncom.2020.00010. eCollection 2020.
Gliomas are the most common primary brain malignancies, with varying degrees of aggressiveness and prognosis. Understanding of tumor biology and intra-tumor heterogeneity is necessary for planning personalized therapy and predicting response to therapy. Accurate tumoral and intra-tumoral segmentation on MRI is the first step toward understanding the tumor biology through computational methods. The purpose of this study was to design a segmentation algorithm and evaluate its performance on pre-treatment brain MRIs obtained from patients with gliomas. In this study, we have designed a novel 3D U-Net architecture that segments various radiologically identifiable sub-regions like edema, enhancing tumor, and necrosis. Weighted patch extraction scheme from the tumor border regions is proposed to address the problem of class imbalance between tumor and non-tumorous patches. The architecture consists of a contracting path to capture context and the symmetric expanding path that enables precise localization. The Deep Convolutional Neural Network (DCNN) based architecture is trained on 285 patients, validated on 66 patients and tested on 191 patients with Glioma from Brain Tumor Segmentation (BraTS) 2018 challenge dataset. Three dimensional patches are extracted from multi-channel BraTS training dataset to train 3D U-Net architecture. The efficacy of the proposed approach is also tested on an independent dataset of 40 patients with High Grade Glioma from our tertiary cancer center. Segmentation results are assessed in terms of Dice Score, Sensitivity, Specificity, and Hausdorff 95 distance (ITCN intra-tumoral classification network). Our proposed architecture achieved Dice scores of 0.88, 0.83, and 0.75 for the whole tumor, tumor core and enhancing tumor, respectively, on BraTS validation dataset and 0.85, 0.77, 0.67 on test dataset. The results were similar on the independent patients' dataset from our hospital, achieving Dice scores of 0.92, 0.90, and 0.81 for the whole tumor, tumor core and enhancing tumor, respectively. The results of this study show the potential of patch-based 3D U-Net for the accurate intra-tumor segmentation. From experiments, it is observed that the weighted patch-based segmentation approach gives comparable performance with the pixel-based approach when there is a thin boundary between tumor subparts.
神经胶质瘤是最常见的原发性脑恶性肿瘤,其侵袭性和预后程度各不相同。了解肿瘤生物学和肿瘤内异质性对于规划个性化治疗和预测治疗反应至关重要。通过计算方法了解肿瘤生物学的第一步是在MRI上进行准确的肿瘤和肿瘤内分割。本研究的目的是设计一种分割算法,并评估其在从神经胶质瘤患者获得的治疗前脑MRI上的性能。在本研究中,我们设计了一种新颖的3D U-Net架构,该架构可分割各种放射学上可识别的子区域,如水肿、强化肿瘤和坏死区域。我们提出了从肿瘤边界区域提取加权补丁的方案,以解决肿瘤补丁和非肿瘤补丁之间的类别不平衡问题。该架构由一个用于捕捉上下文的收缩路径和一个实现精确定位的对称扩展路径组成。基于深度卷积神经网络(DCNN)的架构在285例患者上进行训练,在66例患者上进行验证,并在来自脑肿瘤分割(BraTS)2018挑战数据集的191例神经胶质瘤患者上进行测试。从多通道BraTS训练数据集中提取三维补丁以训练3D U-Net架构。我们还在来自我们三级癌症中心的40例高级别神经胶质瘤患者的独立数据集上测试了所提出方法的有效性。根据骰子分数、敏感性、特异性和豪斯多夫95距离(ITCN肿瘤内分类网络)评估分割结果。我们提出的架构在BraTS验证数据集上对整个肿瘤、肿瘤核心和强化肿瘤的骰子分数分别为0.88、0.83和0.75,在测试数据集上为0.85、0.77和0.67。在我们医院的独立患者数据集上结果相似,整个肿瘤、肿瘤核心和强化肿瘤的骰子分数分别为0.92、0.90和0.81。本研究结果表明基于补丁的3D U-Net在准确的肿瘤内分割方面具有潜力。从实验中观察到,当肿瘤子部分之间边界较薄时,基于加权补丁的分割方法与基于像素的方法具有相当的性能。