肿瘤体积特征可预测弥漫性固有脑桥胶质瘤患者的生存结果。

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2024-08-30 eCollection Date: 2024-01-01 DOI:10.1093/noajnl/vdae151
D'Andre Spencer, Erin R Bonner, Carlos Tor-Díez, Xinyang Liu, Kristen Bougher, Rachna Prasad, Heather Gordish-Dressman, Augustine Eze, Roger J Packer, Javad Nazarian, Marius George Linguraru, Miriam Bornhorst
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引用次数: 0

摘要

背景:弥漫性桥脑胶质瘤(DIPG)是一种致命的儿童中枢神经系统肿瘤。诊断和监测肿瘤对治疗的反应主要依靠磁共振成像(MRI)。基于磁共振成像的肿瘤体积和外观分析有助于预测患者的总生存期(OS):方法:回顾性收集了经影像学确诊的典型DIPG患儿(43例)的对比增强T1和FLAIR/T2加权磁共振图像。对诊断时(43例)和放疗后(40例)的MRI特征进行评估,以确定OS结果预测因素。特征包括三维肿瘤体积(Twv)、对比增强肿瘤核心体积(Tc)、相对于Twv的Tc(TC/Twv)和相对于全脑体积的Twv。支持向量机(SVM)学习被用来识别预测OS结果的特征组合(OS定义为距诊断时间短于或长于12个月):结果:与不良OS结果相关的特征包括诊断时存在对比增强肿瘤、放疗(RT)后Tc/Twv>15%以及放疗后∆Tc/Twv>20%。一致的是,SVM 学习能识别诊断时的 Tc/Twv(预测准确率为 74%)和结论时的ΔTc/Twv:本研究表明,诊断时和 RT 后 4 个月内的肿瘤成像特征可预测 DIPG 的不同 OS 结果。这些发现为将基于肿瘤体积的预测分析纳入临床提供了一个框架,有可能根据肿瘤风险特征和基于机器学习分析的未来应用进行定制化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor volume features predict survival outcomes for patients diagnosed with diffuse intrinsic pontine glioma.

Background: Diffuse intrinsic pontine glioma (DIPG) is a fatal childhood central nervous system tumor. Diagnosis and monitoring of tumor response to therapy is based on magnetic resonance imaging (MRI). MRI-based analyses of tumor volume and appearance may aid in the prediction of patient overall survival (OS).

Methods: Contrast-enhanced T1- and FLAIR/T2-weighted MR images were retrospectively collected from children with classical DIPG diagnosed by imaging (n = 43 patients). MRI features were evaluated at diagnosis (n = 43 patients) and post-radiation (n = 40 patients) to determine OS outcome predictors. Features included 3D tumor volume (Twv), contrast-enhancing tumor core volume (Tc), Tc relative to Twv (TC/Twv), and Twv relative to whole brain volume. Support vector machine (SVM) learning was used to identify feature combinations that predicted OS outcome (defined as OS shorter or longer than 12 months from diagnosis).

Results: Features associated with poor OS outcome included the presence of contrast-enhancing tumor at diagnosis, >15% Tc/Twv post-radiation therapy (RT), and >20% ∆Tc/Twv post-RT. Consistently, SVM learning identified Tc/Twv at diagnosis (prediction accuracy of 74%) and ∆Tc/Twv at <2 months post-RT (accuracy = 75%) as primary features of poor survival.

Conclusions: This study demonstrates that tumor imaging features at diagnosis and within 4 months of RT can predict differential OS outcomes in DIPG. These findings provide a framework for incorporating tumor volume-based predictive analyses into the clinical setting, with the potential for treatment customization based on tumor risk characteristics and future applications of machine-learning-based analysis.

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CiteScore
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