稳健深度学习应对不完整MRI序列:胶质瘤分级与IDH突变预测的大规模多中心研究
该研究基于五个临床机构和公共数据集的2170例胶质瘤患者常规MRI,提出RISEN网络处理不完整序列的放射组学特征,实现胶质瘤分级和IDH突变状态预测。在最佳序列组合T1WI、CE-T1WI和T2-FLAIR下,完整数据验证集AUC较高,模拟缺失场景下性能仅中度下降,真实缺失数据中亦表现稳健。
要点
- T1WI+CE-T1WI+T2-FLAIR为胶质瘤分级和IDH预测的最佳序列组合。
- RISEN可处理缺失序列,模拟缺失下分级和IDH预测AUC仅中度下降。
- 真实临床缺失序列数据中RISEN仍保持较高预测性能。
核心结论
- RISEN在多队列中对胶质瘤分级和IDH突变预测表现出稳健且临床适用的性能,即使面对常见的不完整mp-MRI条件。
研究设计与样本
- 回顾性多中心研究,纳入五个临床机构和公共数据集的2170例胶质瘤患者常规MRI。
- 使用稳健不完整序列估计网络(RISEN)对缺失序列的放射组学特征进行插补并学习潜在融合表示。
- 通过确定最佳mp-MRI序列组合并模拟不同缺失率场景,以AUC评估模型性能。
诊断标准与关键数值
- 完整数据下,T1WI、CE-T1WI和T2-FLAIR组合在内部和外部验证集的胶质瘤分级AUC分别为0.8160、0.9136、0.8031。
- 完整数据下,同一序列组合的IDH预测AUC在内部和外部验证集分别为0.8657、0.8731、0.7682。
- 模拟不完整序列场景下,RISEN分级平均AUC分别为0.7942、0.8955、0.7759。
- 模拟不完整序列场景下,RISEN的IDH预测平均AUC分别为0.8454、0.8478、0.7414。
- 真实世界缺失序列数据中,RISEN的AUC分别为0.8910(分级)和0.8854(IDH预测)。
临床应用与阅片要点
- 在日常阅片遇序列不完整时,可参考RISEN思路利用可用序列进行胶质瘤分级和IDH状态预测。
- 优先保证T1WI、CE-T1WI和T2-FLAIR序列的采集,以支撑最佳模型性能。
局限性
- 原文未明确报告研究局限性。
以上解读依据论文摘要(全文未开放获取或许可不允许翻译转载)。
英文原文(摘要)· 点击展开
OBJECTIVES: Incomplete MRI sequences pose a significant challenge to the reliability of multiparametric MRI (mp-MRI) radiomics models. This study aimed to develop a robust and noninvasive approach for accurate glioma grading and isocitrate dehydrogenase (IDH) mutation status prediction using incomplete MRI data.
MATERIALS AND METHODS: Conventional MRI scans of 2170 glioma patients were retrospectively collected from five clinical institutions and a public dataset. Radiomic features extracted from each sequence, including incomplete ones, were processed using a robust incomplete sequence estimation network (RISEN). This model imputes missing features and learns latent fusion representations for glioma grading and IDH mutation status prediction. Model performance was evaluated by determining the optimal combination of mp-MRI sequences and simulating various clinical scenarios with different rates of missing data, using the area under the curve (AUC).
RESULTS: The optimal sequence combination of T1WI, CE-T1WI, and T2-FLAIR achieved the highest performance for glioma grading (AUC: 0.8160, 0.9136, 0.8031) and IDH prediction (AUC: 0.8657, 0.8731, 0.7682) in internal and external validation datasets with complete data. In simulated incomplete-sequence scenarios, RISEN exhibited only moderate declines for glioma grading (mean AUC: 0.7942, 0.8955, 0.7759) and IDH prediction (mean AUC: 0.8454, 0.8478, 0.7414). Comparable robustness was observed in real-world missing-sequence data (AUC: 0.8910 and 0.8854, respectively).
CONCLUSION: RISEN demonstrates robust and clinically applicable performance for glioma grading and IDH mutation prediction across multiple cohorts, even under commonly encountered incomplete mp-MRI conditions.
KEY POINTS: Question Incomplete MRI sequences present a major challenge for radiomics-based glioma grading and IDH mutation status prediction in real-world clinical settings. Findings The proposed RISEN model imputes missing features using latent representations, improving model robustness and maintaining high predictive performance across various missing data scenarios. Clinical relevance RISEN offers a reliable solution for real-world glioma diagnosis when MRI sequences are incomplete, ensuring consistent clinical decision-making and personalized therapy planning across diverse imaging conditions.
引用
- Liang F, Yan J, Lai S, et al. Robust deep learning for incomplete MRI sequences in glioma grading and IDH mutation status prediction: a large-scale multicenter study. Eur Radiol. 2026. PMID: 42142114. doi:10.1007/s00330-026-12622-4
供执业医师工作参考,不替代临床判断;数值与分级以指南原文为准。