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使用机器学习估计原发性高级别胶质瘤患者的无进展生存期

Estimating Progression-Free Survival in Patients with Primary High-Grade Glioma Using Machine Learning.

作者信息

Kwiatkowska-Miernik Agnieszka, Wasilewski Piotr Gustaw, Mruk Bartosz, Sklinda Katarzyna, Bujko Maciej, Walecki Jerzy

机构信息

Centre of Radiological Diagnostics, National Medical Institute of the Ministry of the Interior and Administration, Wołoska 137, 02-507 Warsaw, Poland.

Department of Neurosurgery, National Medical Institute of the Ministry of the Interior and Administration, Wołoska 137, 02-507 Warsaw, Poland.

出版信息

J Clin Med. 2024 Oct 16;13(20):6172. doi: 10.3390/jcm13206172.

DOI:10.3390/jcm13206172
PMID:39458122
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11508924/
Abstract

: High-grade gliomas are the most common primary malignant brain tumors in adults. These neoplasms remain predominantly incurable due to the genetic diversity within each tumor, leading to varied responses to specific drug therapies. With the advent of new targeted and immune therapies, which have demonstrated promising outcomes in clinical trials, there is a growing need for image-based techniques to enable early prediction of treatment response. This study aimed to evaluate the potential of radiomics and artificial intelligence implementation in predicting progression-free survival (PFS) in patients with highest-grade glioma (CNS WHO 4) undergoing a standard treatment plan. : In this retrospective study, prediction models were developed in a cohort of 51 patients with pathologically confirmed highest-grade glioma (CNS WHO 4) from the authors' institution and the repository of the Cancer Imaging Archive (TCIA). Only patients with confirmed recurrence after complete tumor resection with adjuvant radiotherapy and chemotherapy with temozolomide were included. For each patient, 109 radiomic features of the tumor were obtained from a preoperative magnetic resonance imaging (MRI) examination. Four clinical features were added manually-sex, weight, age at the time of diagnosis, and the lobe of the brain where the tumor was located. The data label was the time to recurrence, which was determined based on follow-up MRI scans. Artificial intelligence algorithms were built to predict PFS in the training set (n = 75%) and then validate it in the test set (n = 25%). The performance of each model in both the training and test datasets was assessed using mean absolute percentage error (MAPE). : In the test set, the random forest model showed the highest predictive performance with 1-MAPE = 92.27% and a C-index of 0.9544. The decision tree, gradient booster, and artificial neural network models showed slightly lower effectiveness with 1-MAPE of 88.31%, 80.21%, and 91.29%, respectively. : Four of the six models built gave satisfactory results. These results show that artificial intelligence models combined with radiomic features could be useful for predicting the progression-free survival of high-grade glioma patients. This could be beneficial for risk stratification of patients, enhancing the potential for personalized treatment plans and improving overall survival. Further investigation is necessary with an expanded sample size and external multicenter validation.

摘要

高级别胶质瘤是成人中最常见的原发性恶性脑肿瘤。由于每个肿瘤内部的基因多样性,这些肿瘤仍然主要无法治愈,导致对特定药物治疗的反应各不相同。随着新的靶向治疗和免疫治疗的出现,它们在临床试验中已显示出有前景的结果,因此越来越需要基于图像的技术来实现对治疗反应的早期预测。本研究旨在评估放射组学和人工智能应用在预测接受标准治疗方案的最高级别胶质瘤(中枢神经系统WHO 4级)患者无进展生存期(PFS)方面的潜力。

在这项回顾性研究中,在来自作者所在机构和癌症影像存档库(TCIA)的51例经病理证实为最高级别胶质瘤(中枢神经系统WHO 4级)的患者队列中开发了预测模型。仅纳入了在肿瘤完全切除后接受辅助放疗和替莫唑胺化疗后确诊复发的患者。对于每位患者,从术前磁共振成像(MRI)检查中获取肿瘤的109个放射组学特征。手动添加了四个临床特征——性别、体重、诊断时的年龄以及肿瘤所在的脑叶。数据标签是复发时间,这是根据后续的MRI扫描确定的。构建人工智能算法以在训练集(n = 75%)中预测PFS,然后在测试集(n = 25%)中进行验证。使用平均绝对百分比误差(MAPE)评估每个模型在训练和测试数据集中的性能。

在测试集中,随机森林模型显示出最高的预测性能,1-MAPE = 92.27%,C指数为0.9544。决策树、梯度提升和人工神经网络模型的有效性略低,1-MAPE分别为88.31%、80.21%和91.29%。

所构建的六个模型中有四个给出了令人满意的结果。这些结果表明,结合放射组学特征的人工智能模型可能有助于预测高级别胶质瘤患者的无进展生存期。这可能有利于患者的风险分层,增强个性化治疗方案的潜力并改善总生存期。需要通过扩大样本量和外部多中心验证进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/efe592e0ec4e/jcm-13-06172-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/39fa7a0cfeae/jcm-13-06172-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/2031e478d240/jcm-13-06172-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/27efa8d94303/jcm-13-06172-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/8b5a7ab89b2c/jcm-13-06172-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/efe592e0ec4e/jcm-13-06172-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/39fa7a0cfeae/jcm-13-06172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/c93580a2dd92/jcm-13-06172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/2031e478d240/jcm-13-06172-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/27efa8d94303/jcm-13-06172-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a303/11508924/efe592e0ec4e/jcm-13-06172-g007.jpg

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