Lin Minhua, Hu Tingting, Yan Ling, Xiao Dongdong, Zhao Hongyang, Yan Pengfei
Department of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
World Neurosurg. 2019 Jul;127:e677-e684. doi: 10.1016/j.wneu.2019.03.241. Epub 2019 Apr 1.
We sought to determine whether systemic inflammatory markers (SIMs) can be used to predict the pathological grade of meningioma before surgery.
Patients with histopathologically proven intracranial meningiomas who had undergone surgery from January 2014 to April 2018 were identified. The 14 most recent SIM levels measured before surgery were retrieved. The Mann-Whitney U test was used to determine the statistically significant differences between groups. Receiver operating characteristic curves were constructed, and the areas under the curve (AUC) were calculated to assess the diagnostic value of each biomarker. Predictive models built with biomarker pairs using logistic regression or support vector machine classifiers were used to assess their combined performance.
A total of 672 patients with 575 and 97 low-grade and high-grade meningiomas, respectively, were investigated. Of the 14 SIMS, 7 differed significantly between the 2 meningioma groups. However, receiver operating characteristic analysis showed that none of these 7 SIMs alone could predict for the meningioma grade; the highest AUC was 0.61. Two biomarkers (erythrocyte and neutrophil/lymphocyte ratio) were incorporated into the logistic regression model; the corresponding AUC was 0.64. Moreover, 21 biomarker pairs were used to train the support vector machine classifiers; the AUCs of 6 pairs were >0.55; the maximum AUC was 0.60.
SIMs obtained from routine preoperative laboratory testing had a limited ability to differentiate low- and high-grade meningioma in our cohort of 672 patients. Further prospective, multicenter studies with larger sample sizes are warranted to confirm this finding.
我们试图确定全身炎症标志物(SIMs)是否可用于术前预测脑膜瘤的病理分级。
确定2014年1月至2018年4月期间接受手术且经组织病理学证实为颅内脑膜瘤的患者。检索术前测量的14项最新SIM水平。采用Mann-Whitney U检验确定组间的统计学显著差异。构建受试者工作特征曲线,并计算曲线下面积(AUC)以评估每个生物标志物的诊断价值。使用逻辑回归或支持向量机分类器构建的生物标志物对预测模型用于评估其联合性能。
共调查了672例患者,其中低级别和高级别脑膜瘤分别为575例和97例。在14项SIMs中,有7项在两组脑膜瘤之间存在显著差异。然而,受试者工作特征分析表明,这7项SIMs单独一项均无法预测脑膜瘤分级;最高AUC为0.61。将两项生物标志物(红细胞和中性粒细胞/淋巴细胞比值)纳入逻辑回归模型;相应的AUC为0.64。此外,使用21对生物标志物训练支持向量机分类器;6对的AUC>0.55;最大AUC为0.60。
在我们672例患者队列中,术前常规实验室检测获得的SIMs区分低级别和高级别脑膜瘤的能力有限。需要进一步开展更大样本量的前瞻性多中心研究来证实这一发现。