多模态深度学习提高了小儿低级别胶质瘤的复发风险预测能力

IF 16.4 1区 医学 Q1 CLINICAL NEUROLOGY
Maryamalsadat Mahootiha, Divyanshu Tak, Zezhong Ye, Anna Zapaishchykova, Jirapat Likitlersuang, Juan Carlos Climent Pardo, Aidan Boyd, Sridhar Vajapeyam, Rishi Chopra, Sanjay P Prabhu, Kevin X Liu, Hesham Elhalawani, Ali Nabavizadeh, Ariana Familiar, Sabine Mueller, Hugo J W L Aerts, Pratiti Bandopadhayay, Keith L Ligon, Daphne Haas-Kogan, Tina Y Poussaint, Hemin Ali Qadir, Ilangko Balasingham, Benjamin H Kann
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引用次数: 0

摘要

背景:小儿低级别胶质瘤(pLGGs)的术后复发风险很难用传统的临床、影像学和基因组学因素来预测。我们研究了磁共振成像肿瘤特征的深度学习能否改善 pLGG 术后风险分层:我们使用专为pLGG分割设计的预训练深度学习(DL)工具,从接受手术的患者术前T2加权MRI中提取pLGG成像特征(DL-MRI特征)。患者来自两家机构:Dana Farber/Boston Children's Hospital (DF/BCH) 和儿童脑肿瘤网络 (CBTN)。我们训练了三种DL逻辑危险模型,以预测术后无事件生存(EFS)概率:1)临床特征;2)DL-MRI特征;3)多模态(临床和DL-MRI特征)。我们用与时间相关的一致性指数(Ctd)对模型进行了评估,并用卡普兰-梅尔图和对数秩检验对风险组进行了分层。我们开发了一个自动流水线,将 pLGG 分割和 EFS 预测与最佳模型整合在一起:在分析的 396 例患者中(中位随访时间:85 个月,范围:1.5-329 个月),214 例(54%)接受了全切,110 例(28%)复发。与 DL-MRI 和临床模型相比,多模态模型改善了 EFS 预测(Ctd:分别为 0.85(95% CI:0.81-0.93)、0.79(95% CI:0.70-0.88)和 0.72(95% CI:0.57-0.77))。多模态模型改善了风险组的分层(预测高风险患者的 3 年 EFS 为 31%,低风险患者为 92%,P 结论:DL提取的成像特征可为pLGG术后复发预测提供依据。多模态 DL 可改善 pLGG 术后风险分层,并可指导术后决策。可能需要更大规模的多中心训练数据来提高模型的普适性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal Deep Learning Improves Recurrence Risk Prediction in Pediatric Low-Grade Gliomas.

Background: Postoperative recurrence risk for pediatric low-grade gliomas (pLGGs) is challenging to predict by conventional clinical, radiographic, and genomic factors. We investigated if deep learning of MRI tumor features could improve postoperative pLGG risk stratification.

Methods: We used pre-trained deep learning (DL) tool designed for pLGG segmentation to extract pLGG imaging features from preoperative T2-weighted MRI from patients who underwent surgery (DL-MRI features). Patients were pooled from two institutions: Dana Farber/Boston Children's Hospital (DF/BCH) and the Children's Brain Tumor Network (CBTN). We trained three DL logistic hazard models to predict postoperative event-free survival (EFS) probabilities with 1) clinical features, 2) DL-MRI features, and 3) multimodal (clinical and DL-MRI features). We evaluated the models with a time-dependent Concordance Index (Ctd) and risk group stratification with Kaplan Meier plots and log-rank tests. We developed an automated pipeline integrating pLGG segmentation and EFS prediction with the best model.

Results: Of the 396 patients analyzed (median follow-up: 85 months, range: 1.5-329 months), 214 (54%) underwent gross total resection and 110 (28%) recurred. The multimodal model improved EFS prediction compared to the DL-MRI and clinical models (Ctd: 0.85 (95% CI: 0.81-0.93), 0.79 (95% CI: 0.70-0.88), and 0.72 (95% CI: 0.57-0.77), respectively). The multimodal model improved risk-group stratification (3-year EFS for predicted high-risk: 31% versus low-risk: 92%, p<0.0001).

Conclusions: DL extracts imaging features that can inform postoperative recurrence prediction for pLGG. Multimodal DL improves postoperative risk stratification for pLGG and may guide postoperative decision-making. Larger, multicenter training data may be needed to improve model generalizability.

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来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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