利用时间深度学习预测小儿胶质瘤的纵向风险。

NEJM AI Pub Date : 2025-05-01 Epub Date: 2025-04-24 DOI:10.1056/aioa2400703
Divyanshu Tak, Biniam A Garomsa, Anna Zapaishchykova, Zezhong Ye, Sridhar Vajapeyam, Maryam Mahootiha, Juan Carlos Climent Pardo, Ceilidh Smith, Ariana M Familiar, Tafadzwa L Chaunzwa, Kevin X Liu, Sanjay P Prabhu, Pratiti Bandopadhayay, Ali Nabavizadeh, Sabine Mueller, Hugo J W L Aerts, Daphne Haas-Kogan, Tina Y Poussaint, Benjamin H Kann
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引用次数: 0

摘要

背景:小儿胶质瘤复发可引起发病率和死亡率;然而,复发模式和严重程度是异质性的,很难用已建立的临床和基因组标记来预测。因此,无论个体复发风险如何,几乎所有儿童都要接受频繁、长期的脑磁共振成像(MRI)监测。对连续MRI扫描进行纵向深度学习分析可能是改善胶质瘤和其他癌症个体化复发预测的有效方法,但到目前为止,进展受到数据可用性和当前机器学习方法的限制。方法:我们开发了一种为纵向医学成像分析量身定制的自监督时间深度学习方法,其中多步骤模型对患者的连续MRI扫描进行编码,并训练以正确的时间顺序分类作为借口任务。然后对预训练模型进行微调,通过利用患者术后监测扫描的历史数据,预测主要关注的终点——在本例中,从最后一次扫描开始预测小儿胶质瘤的1年复发。我们将该模型应用于来自三个独立机构的儿童低级别和高级别胶质瘤设置的715名患者的3994次扫描。结果:与传统方法相比,纵向成像分析与时间学习相比,复发预测性能(F1评分)提高了58.5%(范围,6.6至58.5%),在所有数据集中,低级别和高级别胶质瘤和接受者工作特征曲线下面积(范围,75至89%)的性能都有所提高。复发预测性能随着每位患者可用的历史扫描次数的增加而增加,根据数据集的不同,在3到6次扫描之间达到平台期。结论:时间深度学习可以为儿童脑肿瘤提供高性能的纵向医学成像分析和护理点决策支持。时间学习可能广泛适用于跟踪和预测其他癌症和慢性疾病患者进行监测成像的风险。(部分由美国国立卫生研究院/国家癌症研究所(U54 CA274516和P50 CA165962)和Botha-Chan低级别胶质瘤协会资助。)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Longitudinal Risk Prediction for Pediatric Glioma with Temporal Deep Learning.

Background: Pediatric glioma recurrence can cause morbidity and mortality; however, recurrence patterns and severity are heterogeneous and challenging to predict with established clinical and genomic markers. As a result, almost all children undergo frequent, long-term, magnetic resonance imaging (MRI) brain surveillance regardless of individual recurrence risk. Longitudinal deep-learning analysis of serial MRI scans may be an effective approach for improving individualized recurrence prediction in gliomas and other cancers, but, thus far, progress has been limited by data availability and current machine-learning approaches.

Methods: We developed a self-supervised temporal deep-learning approach tailored for longitudinal medical imaging analysis, wherein a multistep model encodes patients' serial MRI scans and is trained to classify the correct chronological order as a pretext task. The pretrained model is then fine-tuned to predict the primary end point of interest - in this case, 1-year recurrence prediction for pediatric gliomas from the point of last scan - by leveraging a patient's historical postoperative surveillance scans. We apply the model across 3994 scans from 715 patients followed at three separate institutions in the setting of pediatric low- and high-grade gliomas.

Results: Longitudinal imaging analysis with temporal learning improved recurrence prediction performance (F1 score) by up to 58.5% (range, 6.6 to 58.5%) compared with traditional approaches across datasets, with performance improvements in both low- and high-grade gliomas and area under the receiver operating characteristic curve of (range, 75 to 89%) across all datasets. Recurrence prediction performance increased incrementally with the number of historical scans available per patient, reaching plateaus between three and six scans, depending on the dataset.

Conclusions: Temporal deep learning enables high-performing longitudinal medical imaging analysis and point-of-care decision support for pediatric brain tumors. Temporal learning may be broadly adaptable to track and predict risk in patients with other cancers and chronic diseases undergoing surveillance imaging. (Funded in part by the National Institutes of Health/National Cancer Institute (U54 CA274516 and P50 CA165962), and Botha-Chan Low Grade Glioma Consortium.).

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