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首页> 外文期刊>Journal of neuro-oncology. >Non-invasive genotype prediction of chromosome 1p/19q co-deletion by development and validation of an MRI-based radiomics signature in lower-grade gliomas
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Non-invasive genotype prediction of chromosome 1p/19q co-deletion by development and validation of an MRI-based radiomics signature in lower-grade gliomas

机译:染色体1P / 19Q次级胶质瘤中MRI基辐射瘤签发的染色体1P / 19Q共缺失的非侵入基因型预测

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Purpose To perform radiomics analysis for non-invasively predicting chromosome lp/19q co-deletion in World Health Organization grade II and III (lower-grade) gliomas. Methods This retrospective study included 277 patients histopathologically diagnosed with lower-grade glioma. Clinical parameters were recorded for each patient. We performed a radiomics analysis by extracting 647 MRI-based features and applied the random forest algorithm to generate a radiomics signature for predicting 1p/19q co-deletion in the training cohort (n = 184). The clinical model consisted of pertinent clinical factors, and was built using a logistic regression algorithm. A combined model, incorporating both the radiomics signature and related clinical factors, was also constructed. The receiver operating characteristics curve was used to evaluate the predictive performance. We further validated the predictability of the three developed models using a time-independent validation cohort (n = 93). Results The radiomics signature was constructed as an independent predictor for differentiating lp/19q co-deletion genotypes, which demonstrated superior performance on both the training and validation cohorts with areas under curve (AUCs) of 0.887 and 0.760, respectively. These results outperformed the clinical model (AUCs of 0.580 and 0.627 on training and validation cohorts). The AUCs of the combined model were 0.885 and 0.753 on training and validation cohorts, respectively, which indicated that clinical factors did not present additional improvement for the prediction. Conclusion Our study highlighted that an MRI-based radiomics signature can effectively identify the lp/19q co-deletion in histopathologically diagnosed lower-grade gliomas, thereby offering the potential to facilitate non-invasive molecular subtype prediction of gliomas.
机译:目的在世界卫生组织II和III(较低级)胶质组织中对非侵入性预测染色体LP / 19Q共缺失进行辐射瘤分析。方法本回顾性研究包括277名患者组织病理学诊断为较低级胶质瘤。每位患者记录临床参数。我们通过提取基于647个MRI的特征来进行辐射瘤分析,并应用随机林算法来生成用于预测训练队列中的1P / 19Q共缺陷的辐射族签名(n = 184)。临床模型由相关的临床因素组成,并使用逻辑回归算法建造。还构建了一种组合模型,包括辐射瘤签名和相关的临床因素。接收器操作特性曲线用于评估预测性能。我们进一步验证了使用时间无关的验证队列(n = 93)的三个开发模型的可预测性。结果,辐射瘤构建为分化LP / 19Q共缺失基因型的独立预测因子,其在训练和验证队列中分别展示了0.887和0.760的曲线区域(AUC)的训练和验证队列的优异性能。这些结果表现优于临床模型(培训和验证队列0.580和0.627的AUC)。培训和验证队列的组合模式的AUC分别为0.885和0.753,这表明临床因素对预测并未额外改进。结论我们的研究强调,基于MRI的辐射瘤特征可以有效地识别组织病理学诊断的较低级胶质瘤中的LP / 19Q共缺失,从而提供了促进胶质瘤的非侵入性分子亚型预测的可能性。

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