A multicenter study on deep learning for glioblastoma auto-segmentation with prior knowledge in multimodal imaging

IF 4.5 2区 医学 Q1 ONCOLOGY Cancer Science Pub Date : 2024-08-09 DOI:10.1111/cas.16304
Suqing Tian, Yinglong Liu, Xinhui Mao, Xin Xu, Shumeng He, Lecheng Jia, Wei Zhang, Peng Peng, Junjie Wang
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Abstract

A precise radiotherapy plan is crucial to ensure accurate segmentation of glioblastomas (GBMs) for radiation therapy. However, the traditional manual segmentation process is labor-intensive and heavily reliant on the experience of radiation oncologists. In this retrospective study, a novel auto-segmentation method is proposed to address these problems. To assess the method's applicability across diverse scenarios, we conducted its development and evaluation using a cohort of 148 eligible patients drawn from four multicenter datasets and retrospective data collection including noncontrast CT, multisequence MRI scans, and corresponding medical records. All patients were diagnosed with histologically confirmed high-grade glioma (HGG). A deep learning-based method (PKMI-Net) for automatically segmenting gross tumor volume (GTV) and clinical target volumes (CTV1 and CTV2) of GBMs was proposed by leveraging prior knowledge from multimodal imaging. The proposed PKMI-Net demonstrated high accuracy in segmenting, respectively, GTV, CTV1, and CTV2 in an 11-patient test set, achieving Dice similarity coefficients (DSC) of 0.94, 0.95, and 0.92; 95% Hausdorff distances (HD95) of 2.07, 1.18, and 3.95 mm; average surface distances (ASD) of 0.69, 0.39, and 1.17 mm; and relative volume differences (RVD) of 5.50%, 9.68%, and 3.97%. Moreover, the vast majority of GTV, CTV1, and CTV2 produced by PKMI-Net are clinically acceptable and require no revision for clinical practice. In our multicenter evaluation, the PKMI-Net exhibited consistent and robust generalizability across the various datasets, demonstrating its effectiveness in automatically segmenting GBMs. The proposed method using prior knowledge in multimodal imaging can improve the contouring accuracy of GBMs, which holds the potential to improve the quality and efficiency of GBMs' radiotherapy.

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利用多模态成像中的先验知识对胶质母细胞瘤自动分割进行深度学习的多中心研究。
精确的放射治疗计划对于确保准确分割胶质母细胞瘤(GBM)以进行放射治疗至关重要。然而,传统的人工分割过程耗费大量人力,而且严重依赖放射肿瘤专家的经验。在这项回顾性研究中,提出了一种新型自动分割方法来解决这些问题。为了评估该方法在不同情况下的适用性,我们从四个多中心数据集和回顾性数据收集(包括非对比 CT、多序列 MRI 扫描和相应的医疗记录)中抽取了 148 名符合条件的患者,对其进行了开发和评估。所有患者均经组织学确诊为高级别胶质瘤(HGG)。通过利用多模态成像的先验知识,提出了一种基于深度学习的方法(PKMI-Net),用于自动分割GBM的肿瘤总体积(GTV)和临床目标体积(CTV1和CTV2)。所提出的 PKMI-Net 在 11 名患者的测试集中分别对 GTV、CTV1 和 CTV2 进行了高精度分割,Dice 相似系数 (DSC) 分别达到 0.94、0.95 和 0.92;95% Hausdorff 距离 (HD95) 分别为 2.07、1.18 和 3.95 毫米;平均表面距离 (ASD) 分别为 0.69、0.39 和 1.17 毫米;相对体积差异 (RVD) 分别为 5.50%、9.68% 和 3.97%。此外,PKMI-Net 生成的绝大多数 GTV、CTV1 和 CTV2 在临床上都是可以接受的,无需在临床实践中进行修改。在我们的多中心评估中,PKMI-Net 在各种数据集上都表现出了一致而强大的通用性,证明了它在自动分割 GBM 方面的有效性。利用多模态成像中的先验知识提出的方法可以提高 GBM 的轮廓准确性,从而有望提高 GBM 放疗的质量和效率。
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来源期刊
Cancer Science
Cancer Science 医学-肿瘤学
自引率
3.50%
发文量
406
审稿时长
2 months
期刊介绍: Cancer Science (formerly Japanese Journal of Cancer Research) is a monthly publication of the Japanese Cancer Association. First published in 1907, the Journal continues to publish original articles, editorials, and letters to the editor, describing original research in the fields of basic, translational and clinical cancer research. The Journal also accepts reports and case reports. Cancer Science aims to present highly significant and timely findings that have a significant clinical impact on oncologists or that may alter the disease concept of a tumor. The Journal will not publish case reports that describe a rare tumor or condition without new findings to be added to previous reports; combination of different tumors without new suggestive findings for oncological research; remarkable effect of already known treatments without suggestive data to explain the exceptional result. Review articles may also be published.
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Issue Information In this issue Issue Information In this issue Real-world genome profiling in Japanese patients with pancreatic ductal adenocarcinoma focusing on HRD implications
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