Jiang Haihui, Yu Kefu, Li Mingxiao, Cui Yong, Ren Xiaohui, Yang Chuanwei, Zhao Xuzhe, Lin Song
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
National Clinical Research Center for Neurological Diseases, Center of Brain Tumor, Beijing Institute for Brain Disorders and Beijing Key Laboratory of Brain Tumor, Beijing, China.
Front Oncol. 2020 Nov 3;10:590648. doi: 10.3389/fonc.2020.590648. eCollection 2020.
This study was designed to explore the progression patterns of IDH-wildtype glioblastoma (GBM) at first recurrence after chemoradiotherapy.
Records from 247 patients who underwent progression after diagnosis of IDH-wildtype GBM was retrospectively reviewed. Progression patterns were classified as either local, distant, subependymal or leptomeningeal dissemination based on the preoperative and serial postoperative radiographic images. The clinical and molecular characteristics of different progression patterns were analyzed.
A total of 186 (75.3%) patients had local progression, 15 (6.1%) patients had distant progression, 33 (13.3%) patients had subependymal dissemination, and 13 (5.3%) patients had leptomeningeal dissemination. The most favorable survival occurred in patients with local progression, while no significant difference of survival was found among patients with distant progression, subependymal or leptomeningeal dissemination who were thereby reclassified into non-local group. Multivariable analysis showed that chemotherapy was a protective factor for non-local progression, while gender of male, subventricular zone (SVZ) involvement and O-methylguanine-DNA-methyltransferase (MGMT) promoter methylation were confirmed as risk factors for non-local progression ( < 0.05). Based on the factors screened by multivariable analysis, a nomogram was constructed which conferred high accuracy in predicting non-local progression. Patients in non-local group could be divided into long- and short-term survivors who differed in the rates of SVZ involvement, MGMT promoter methylation and reirradiation ( < 0.05), and a nomogram integrating these factors showed high accuracy in predicting long-term survivors.
Patients harboring different progression patterns conferred distinct clinical and molecular characteristics. Our nomograms could provide theoretical references for physicians to make more personalized and precise treatment decisions.
本研究旨在探讨异柠檬酸脱氢酶(IDH)野生型胶质母细胞瘤(GBM)放化疗后首次复发的进展模式。
回顾性分析247例IDH野生型GBM诊断后出现进展的患者记录。根据术前及术后系列影像学图像,将进展模式分为局部、远处、室管膜下或软脑膜播散。分析不同进展模式的临床和分子特征。
共有186例(75.3%)患者出现局部进展,15例(6.1%)患者出现远处进展,33例(13.3%)患者出现室管膜下播散,13例(5.3%)患者出现软脑膜播散。局部进展患者的生存情况最佳,而远处进展、室管膜下或软脑膜播散患者(因此重新分类为非局部组)的生存无显著差异。多变量分析显示,化疗是非局部进展的保护因素,而男性性别、脑室下区(SVZ)受累及O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化被确认为非局部进展的危险因素(P<0.05)。基于多变量分析筛选出的因素构建了列线图,其在预测非局部进展方面具有较高的准确性。非局部组患者可分为长期和短期生存者,他们在SVZ受累率、MGMT启动子甲基化和再放疗方面存在差异(P<0.05),整合这些因素的列线图在预测长期生存者方面具有较高的准确性。
具有不同进展模式的患者具有不同的临床和分子特征。我们的列线图可为医生做出更个性化和精确的治疗决策提供理论参考。