Suppr超能文献

T2-FLAIR不匹配征对异柠檬酸脱氢酶(IDH)突变型、1p/19q未缺失低级别胶质瘤的预测准确性:一项更新的系统评价和Meta分析

Predictive accuracy of T2-FLAIR mismatch sign for the IDH-mutant, 1p/19q noncodeleted low-grade glioma: An updated systematic review and meta-analysis.

作者信息

Do Yoon Ah, Cho Se Jin, Choi Byung Se, Baik Sung Hyun, Bae Yun Jung, Sunwoo Leonard, Jung Cheolkyu, Kim Jae Hyoung

机构信息

Department of Radiology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.

出版信息

Neurooncol Adv. 2022 Jan 27;4(1):vdac010. doi: 10.1093/noajnl/vdac010. eCollection 2022 Jan-Dec.

Abstract

BACKGROUND

The T2-fluid-attenuated inversion recovery (FLAIR) mismatch sign, has been considered a highly specific imaging biomarker of IDH-mutant, 1p/19q noncodeleted low-grade glioma. This systematic review and meta-analysis aimed to evaluate the diagnostic performance of T2-FLAIR mismatch sign for prediction of a patient with IDH-mutant, 1p/19q noncodeleted low-grade glioma, and identify the causes responsible for the heterogeneity across the included studies.

METHODS

A systematic literature search in the Ovid-MEDLINE and EMBASE databases was performed for studies reporting the relevant topic before November 17, 2020. The pooled sensitivity and specificity values with their 95% confidence intervals were calculated using bivariate random-effects modeling. Meta-regression analyses were also performed to determine factors influencing heterogeneity.

RESULTS

For all the 10 included cohorts from 8 studies, the pooled sensitivity was 40% (95% confidence interval [CI] 28-53%), and the pooled specificity was 100% (95% CI 95-100%). In the hierarchic summary receiver operating characteristic curve, the difference between the 95% confidence and prediction regions was relatively large, indicating heterogeneity among the studies. Higgins I statistics demonstrated considerable heterogeneity in sensitivity (I = 83.5%) and considerable heterogeneity in specificity (I = 95.83%). Among the potential covariates, it seemed that none of factors was significantly associated with study heterogeneity in the joint model. However, the specificity was increased in studies with all the factors based on the differences in the composition of the detailed tumors.

CONCLUSIONS

The T2-FLAIR mismatch sign is near-perfect specific marker of IDH mutation and 1p/19q noncodeletion.

摘要

背景

T2液体衰减反转恢复(FLAIR)不匹配征被认为是异柠檬酸脱氢酶(IDH)突变、1p/19q未缺失的低级别胶质瘤的一种高度特异的影像学生物标志物。本系统评价和荟萃分析旨在评估T2-FLAIR不匹配征对IDH突变、1p/19q未缺失的低级别胶质瘤患者的诊断效能,并确定纳入研究中异质性的原因。

方法

在Ovid-MEDLINE和EMBASE数据库中进行系统文献检索,以查找2020年11月17日前报道相关主题的研究。使用双变量随机效应模型计算合并敏感性和特异性值及其95%置信区间。还进行了荟萃回归分析以确定影响异质性的因素。

结果

对于来自8项研究的所有10个纳入队列,合并敏感性为40%(95%置信区间[CI]28-53%),合并特异性为100%(95%CI 95-100%)。在分层汇总接受者操作特征曲线中,95%置信区间和预测区间之间的差异相对较大,表明研究之间存在异质性。Higgins I统计显示敏感性存在相当大的异质性(I=83.5%),特异性也存在相当大的异质性(I=95.83%)。在潜在的协变量中,在联合模型中似乎没有因素与研究异质性显著相关。然而,基于详细肿瘤组成的差异,在具有所有因素的研究中特异性有所增加。

结论

T2-FLAIR不匹配征是IDH突变和1p/19q未缺失的近乎完美的特异性标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b63/8859831/3ec459338c87/vdac010f0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验