Department of Electronics and Informatics (ETRO), Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Department of Radiology and Medical Imaging, Cliniques Universitaires Saint Luc, Université Catholique de Louvain (UCLouvain), Brussels, Belgium.
Int J Comput Assist Radiol Surg. 2024 Oct;19(10):2101-2109. doi: 10.1007/s11548-024-03238-4. Epub 2024 Aug 2.
Automated glioblastoma segmentation from magnetic resonance imaging is generally performed on a four-modality input, including T1, contrast T1, T2 and FLAIR. We hypothesize that information redundancy is present within these image combinations, which can possibly reduce a model's performance. Moreover, for clinical applications, the risk of encountering missing data rises as the number of required input modalities increases. Therefore, this study aimed to explore the relevance and influence of the different modalities used for MRI-based glioblastoma segmentation.
After the training of multiple segmentation models based on nnU-Net and SwinUNETR architectures, differing only in their amount and combinations of input modalities, each model was evaluated with regard to segmentation accuracy and epistemic uncertainty.
Results show that T1CE-based segmentation (for enhanced tumor and tumor core) and T1CE-FLAIR-based segmentation (for whole tumor and overall segmentation) can reach segmentation accuracies comparable to the full-input version. Notably, the highest segmentation accuracy for nnU-Net was found for a three-input configuration of T1CE-FLAIR-T1, suggesting the confounding effect of redundant input modalities. The SwinUNETR architecture appears to suffer less from this, where said three-input and the full-input model yielded statistically equal results.
The T1CE-FLAIR-based model can therefore be considered as a minimal-input alternative to the full-input configuration. Addition of modalities beyond this does not statistically improve and can even deteriorate accuracy, but does lower the segmentation uncertainty.
从磁共振成像(MRI)自动分割脑胶质瘤通常基于四模态输入,包括 T1、对比 T1、T2 和 FLAIR。我们假设这些图像组合中存在信息冗余,这可能会降低模型的性能。此外,对于临床应用,所需输入模态数量的增加会增加遇到缺失数据的风险。因此,本研究旨在探索基于 MRI 的脑胶质瘤分割中使用的不同模态的相关性和影响。
在基于 nnU-Net 和 SwinUNETR 架构的多个分割模型的训练之后,这些模型仅在输入模态的数量和组合上有所不同,然后评估每个模型的分割准确性和认知不确定性。
结果表明,基于 T1CE 的分割(用于增强肿瘤和肿瘤核心)和基于 T1CE-FLAIR 的分割(用于整个肿瘤和整体分割)可以达到与全输入版本相当的分割准确性。值得注意的是,nnU-Net 的最高分割准确性是在 T1CE-FLAIR-T1 的三输入配置下发现的,这表明冗余输入模态的混杂效应。SwinUNETR 架构似乎受此影响较小,三输入模型和全输入模型的结果在统计学上相等。
因此,基于 T1CE-FLAIR 的模型可以被视为全输入配置的最小输入替代方案。在此基础上添加模态不会在统计学上提高准确性,甚至可能降低准确性,但会降低分割不确定性。