A multimodal fusion network based on variational autoencoder for distinguishing SCLC brain metastases from NSCLC brain metastases.

Medical physics Pub Date : 2025-05-02 DOI:10.1002/mp.17816
Xue Linyan, Cao Jie, Zhou Kexuan, Chen Houquan, Qi Chaoyi, Yin Xiaosong, Wang Jianing, Yang Kun
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Abstract

Background: Distinguishing small cell lung cancer brain metastases from non-small cell lung cancer brain metastases in MRI sequence images is crucial for the accurate diagnosis and treatment of lung cancer brain metastases. Multi-MRI modalities provide complementary and comprehensive information, but efficiently merging these sequences to achieve modality complementarity is challenging due to redundant information within radiomic features and heterogeneity across different modalities.

Purpose: To address these challenges, we propose a novel multimodal fusion network, termed MFN-VAE, which utilizes a variational auto-encoder (VAE) to compress and aggregate radiomic features derived from MRI images.

Methods: Initially, we extract radiomic features from areas of interest in MRI images across T1WI, FLAIR, and DWI modalities. A VAE encoder is then constructed to project these multimodal features into a latent space, where they are decoded into reconstruction features using a decoder. The encoder-decoder network is trained to extract the underlying feature representation of each modality, capturing both the consistency and specificity of each domain.

Results: Experimental results on our collected dataset of lung cancer brain metastases demonstrate the encouraging performance of our proposed MFN-VAE. The method achieved a 0.888 accuracy and a 0.920 AUC (area under the curve), outperforming state-of-the-art methods across different modal combinations.

Conclusions: In this study, we introduce the MFN-VAE, a new multimodal fusion network for differentiating small cell from non-small cell lung cancer brain metastases. Tested on a private dataset, MFN-VAE demonstrated high accuracy (ACC: 0.888; AUC: 0.920), effectively distinguishing between small cell lung cancer brain metastases (SCLC) and non-small cell lung cancer (NSCLC). The SHapley Additive explanation (SHAP) method was used to enhance model interpretability, providing clinicians with a reliable diagnostic tool. Overall, MFN-VAE shows great potential in improving the diagnosis and treatment of lung cancer brain metastases.

基于变分自编码器的多模态融合网络用于区分SCLC脑转移与NSCLC脑转移。
背景:在MRI序列图像中区分小细胞肺癌脑转移与非小细胞肺癌脑转移对于肺癌脑转移的准确诊断和治疗至关重要。多核磁共振成像模式提供了互补和全面的信息,但由于放射学特征中的冗余信息和不同模式的异质性,有效地合并这些序列以实现模式互补是具有挑战性的。目的:为了解决这些挑战,我们提出了一种新的多模态融合网络,称为MFN-VAE,它利用变分自编码器(VAE)压缩和聚合来自MRI图像的放射特征。方法:首先,我们通过T1WI、FLAIR和DWI模式从MRI图像中感兴趣的区域提取放射学特征。然后构建VAE编码器将这些多模态特征投影到潜在空间中,在潜在空间中使用解码器将它们解码为重建特征。编码器-解码器网络被训练以提取每个模态的底层特征表示,捕获每个域的一致性和特异性。结果:在我们收集的肺癌脑转移数据集上的实验结果表明,我们提出的MFN-VAE具有令人鼓舞的性能。该方法获得了0.888的精度和0.920的AUC(曲线下面积),在不同的模态组合中优于最先进的方法。结论:在这项研究中,我们介绍了MFN-VAE,一个新的多模式融合网络,用于区分小细胞和非小细胞肺癌脑转移。在私有数据集上测试,MFN-VAE显示出较高的准确率(ACC: 0.888;AUC: 0.920),有效区分小细胞肺癌脑转移(SCLC)和非小细胞肺癌(NSCLC)。采用SHapley加性解释(SHAP)方法提高模型的可解释性,为临床医生提供可靠的诊断工具。总之,MFN-VAE在改善肺癌脑转移的诊断和治疗方面显示出巨大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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