AB038.建立可靠的半自动分割方法,评估化放疗对非肿瘤脑部的影响

IF 2.1 4区 医学 Q3 ONCOLOGY Chinese clinical oncology Pub Date : 2024-08-01 DOI:10.21037/cco-24-ab038
Eu Jin Lim, Nicole Keong Chwee Har
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引用次数: 0

摘要

背景:目前基于体素的形态计量学(VBM)研究化放疗对多形性胶质母细胞瘤(GBM)大脑健康组织的影响,面临着神经解剖学失真(肿瘤、肿瘤水肿和切除腔)的挑战,而且由于缺乏公认的软件包,不同研究之间的比较有限。我们的目的是比较目前的半自动分割方法,并对其进行优化,以提高研究化放疗对 GBM 患者影响的可靠性:方法:根据预定义的纳入和排除标准,使用公开可用的数据集。对 VBM 管道 CAT12 和 FSL 进行了测试和优化,以减少神经解剖失真的影响。筛选 T1 加权图像,并用 FSL 和 CAT12 进行后处理。用 Wilcoxon 符号秩检验计算和分析了化疗前后全脑、含瘤半球和非含瘤半球的灰质(GM)、白质(WM)和脑脊液(CSF)体积。使用Bland-Altman图和类内相关系数(ICC)评估FSL和CAT12之间的一致性:结果:化疗后全脑的GM体积明显缩小,CSF体积呈代偿性明显增大,而WM体积无明显变化。含肿瘤半球和非含肿瘤半球的趋势相似。Bland-Altman图显示,FSL和CAT12处理后的全脑、含肿瘤半球和非含肿瘤半球的GM和WM体积之间有很好的一致性。非含肿瘤半球的 GM [0.70 (0.53-0.82)] 和 WM [0.75 (0.60-0.85)] 体积以及全脑的 WM [0.71 (0.55-0.83)] 体积的 ICC 均≥0.70。含肿瘤半球的 GM 容量具有良好的一致性,但令人惊讶的是,一致性较差 [0.50 (0.25-0.68)]。与全脑[0.49 (0.25-0.67)]和含肿瘤半球 CSF [0.36 (0.10-0.58)]体积相比,非含肿瘤半球 CSF 体积的一致性和一致性[0.55 (0.32-0.71)]更好。目测结果显示,CAT12和FSL在神经解剖变形的情况下都会出现误判,但CAT12在血肿的情况下更容易出现误判:结论:由于神经解剖变形,化放疗对肿瘤切除术后大脑影响的 VBM 研究仍具有挑战性。可靠的替代方法是使用无解剖学变形的非肿瘤半球。如果使用含肿瘤的大脑,FSL 是更合适的选择,尤其是在存在血肿变形的情况下。
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AB038. Establishing a reliable semi-automated segmentation method for assessing chemoradiotherapy effects on the non-tumoral brain.

Background: Current voxel-based morphometry (VBM) studies of chemoradiotherapy effects on healthy tissues of the glioblastoma multiforme (GBM) brain face a challenge with neuroanatomical distortions (tumor, tumor edema, and resection cavities) and limited comparisons can be drawn across studies due to lack of a universally accepted software package. Our aim is to compare current semi-automated segmentation methods and optimize them for reliability in investigating the effects of chemoradiotherapy on GBM patients.

Methods: A publicly available dataset was used based on predefined inclusion and exclusion criteria. VBM pipelines CAT12 and FSL were tested and optimized to reduce the impact of neuroanatomical distortions. T1-weighted images were screened, and post-processed with FSL and CAT12. Gray matter (GM) and white matter (WM), and cerebrospinal fluid (CSF) volumes of whole brain, tumour-containing and non-tumor containing hemispheres, pre- and post-chemoradiotherapy were calculated and analyzed with Wilcoxon signed-rank tests. Agreement and consistency between FSL and CAT12 were assessed using Bland-Altman plots and intraclass correlation coefficients (ICCs).

Results: Post-chemoradiotherapy GM volumes were significantly reduced in whole brain with a compensatory significant increase in CSF volumes, while WM volumes had no significant changes. Similar trends were noted in tumor-containing and non-tumor-containing hemispheres. Bland-Altman plots showed good agreement between FSL and CAT12 processed GM and WM volumes of whole brain, tumor-containing, and non-tumor-containing hemispheres. ICC ≥0.70 was observed in GM [0.70 (0.53-0.82)] and WM [0.75 (0.60-0.85)] volumes of non-tumor-containing hemisphere, and WM [0.71 (0.55-0.83)] volumes of whole brain. GM volumes of tumor-containing hemisphere had good agreement but surprisingly, poor consistency [0.50 (0.25-0.68)]. CSF volumes in non-tumor-containing hemisphere had better agreement and consistency [0.55 (0.32-0.71)] than whole brain [0.49 (0.25-0.67)] and tumor-containing hemisphere CSF [0.36 (0.10-0.58)] volumes. Visual inspection revealed both CAT12 and FSL mis-segmented in the presence of neuroanatomical distortion although CAT12 was more susceptible in the presence of a hematoma.

Conclusions: VBM studies of chemoradiotherapy effects on the brain post-tumor resection remain challenging due to neuroanatomical distortions. A reliable alternative is to use non-tumor-containing hemispheres with no anatomical distortion. Should tumor-containing brains be used, FSL is a more suitable choice, especially in the presence of hematoma distortion.

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期刊介绍: The Chinese Clinical Oncology (Print ISSN 2304-3865; Online ISSN 2304-3873; Chin Clin Oncol; CCO) publishes articles that describe new findings in the field of oncology, and provides current and practical information on diagnosis, prevention and clinical investigations of cancer. Specific areas of interest include, but are not limited to: multimodality therapy, biomarkers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to cancer. The aim of the Journal is to provide a forum for the dissemination of original research articles as well as review articles in all areas related to cancer. It is an international, peer-reviewed journal with a focus on cutting-edge findings in this rapidly changing field. To that end, Chin Clin Oncol is dedicated to translating the latest research developments into best multimodality practice. The journal features a distinguished editorial board, which brings together a team of highly experienced specialists in cancer treatment and research. The diverse experience of the board members allows our editorial panel to lend their expertise to a broad spectrum of cancer subjects.
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