Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Radiology and Center for Imaging Sciences, Samsung Medical Center, Sungkyungkwan University School of Medicine, Seoul, Korea.
J Neurooncol. 2024 Jun;168(2):239-247. doi: 10.1007/s11060-024-04656-9. Epub 2024 May 3.
There is lack of comprehensive analysis evaluating the impact of clinical, molecular, imaging, and surgical data on survival of patients with gliomatosis cerebri (GC). This study aimed to investigate prognostic factors of GC in adult-type diffuse glioma patients.
Retrospective chart and imaging review was performed in 99 GC patients from adult-type diffuse glioma (among 1,211 patients; 6 oligodendroglioma, 16 IDH-mutant astrocytoma, and 77 IDH-wildtype glioblastoma) from a single institution between 2005 and 2021. Predictors of overall survival (OS) of entire patients and IDH-wildtype glioblastoma patients were determined.
The median OS was 16.7 months (95% confidence interval [CI] 14.2-22.2) in entire patients and 14.3 months (95% CI 12.2-61.9) in IDH-wildtype glioblastoma patients. In entire patients, KPS (hazard ratio [HR] = 0.98, P = 0.004), no 1p/19q codeletion (HR = 10.75, P = 0.019), MGMTp methylation (HR = 0.54, P = 0.028), and hemorrhage (HR = 3.45, P = 0.001) were independent prognostic factors on multivariable analysis. In IDH-wildtype glioblastoma patients, KPS (HR = 2.24, P = 0.075) was the only independent prognostic factor on multivariable analysis. In subgroup of IDH-wildtype glioblastoma with CE tumors, total resection of CE tumor did not remain as a significant prognostic factor (HR = 1.13, P = 0.685).
The prognosis of GC patients is determined by its underlying molecular type and patient performance status. Compared with diffuse glioma without GC, aggressive surgery of CE tumor in GC patients does not improve survival.
目前缺乏全面分析评估临床、分子、影像学和手术数据对大脑胶质瘤病(gliomatosis cerebri,GC)患者生存的影响。本研究旨在探讨成人弥漫性胶质瘤患者中 GC 的预后因素。
回顾性分析了 2005 年至 2021 年间,一家医疗机构收治的 1211 例成人弥漫性胶质瘤患者(其中 6 例为少突胶质细胞瘤,16 例 IDH 突变型星形细胞瘤,77 例 IDH 野生型胶质母细胞瘤)中 99 例 GC 患者的病历和影像学资料。确定了整体患者和 IDH 野生型胶质母细胞瘤患者的总生存期(overall survival,OS)的预测因素。
整体患者的中位 OS 为 16.7 个月(95%置信区间 [CI] 14.2-22.2),IDH 野生型胶质母细胞瘤患者的中位 OS 为 14.3 个月(95% CI 12.2-61.9)。在整体患者中,KPS(风险比 [HR] = 0.98,P = 0.004)、无 1p/19q 缺失(HR = 10.75,P = 0.019)、MGMTp 甲基化(HR = 0.54,P = 0.028)和出血(HR = 3.45,P = 0.001)是多变量分析的独立预后因素。在 IDH 野生型胶质母细胞瘤患者中,KPS(HR = 2.24,P = 0.075)是多变量分析中的唯一独立预后因素。在 IDH 野生型伴 CE 肿瘤的胶质母细胞瘤亚组中,CE 肿瘤的完全切除不再是显著的预后因素(HR = 1.13,P = 0.685)。
GC 患者的预后取决于其潜在的分子类型和患者的一般状态。与无 GC 的弥漫性胶质瘤相比,GC 患者的 CE 肿瘤的积极手术并不能改善生存。