Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA; Department of Neurosurgery, Stanford University School of Medicine, Stanford, California, USA.
Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA.
World Neurosurg. 2019 Aug;128:e217-e224. doi: 10.1016/j.wneu.2019.04.103. Epub 2019 Apr 19.
There is a lack of literature guiding treatment of giant cell glioblastoma (gcGBM), a rare subtype of glioblastoma (GBM). We used a national hospital-based registry to explore treatment patterns and outcomes associated with gcGBM.
Adult patients (age ≥18 years) diagnosed with gcGBM or GBM between 2004 and 2014 were identified from the National Cancer Database. χ analysis and Wilcoxon rank sum testing were used to compare characteristics between the gcGBM and GBM cohorts. Kaplan-Meier statistics, univariable and multivariable Cox regression, and propensity score matching were used to evaluate association between patient, tumor and treatment factors, and survival outcomes. Correlation analysis was used to evaluate historical trends in the treatment of gcGBM. Landmark analysis allowed for accounting of immortal time.
In total, 683 patients with gcGBM were identified. Patients with gcGBM had improved survival compared with patients with GBM (15.5 months from landmark vs. 11.7; P < 0.001). Increased age (P < 0.001) was associated with worse survival whereas being of female sex (P = 0.023) and having a median income >$63,000 (P = 0.004) predisposed patients to improved outcomes. Patients receiving trimodal therapy (biopsy and/or surgery, radiotherapy, and chemotherapy) experienced better outcomes compared with those receiving either biopsy and/or surgery only or biopsy and/or surgery and radiotherapy without systemic therapy (median survival, 17.55 months vs. 6.68 months; P < 0.001).
gcGBM has favorable prognosis compared with GBM and should be aggressively managed with trimodal therapy. Prospective studies of gcGBM are warranted to better characterize gcGBM treatment outcomes.
胶质母细胞瘤(GBM)中有一个罕见的亚型,巨细胞型 GBM(gcGBM),目前缺乏针对其治疗的文献指导。我们利用全国医院的注册数据库,探讨 gcGBM 的治疗模式和预后。
从国家癌症数据库中确定了 2004 年至 2014 年间诊断为 gcGBM 或 GBM 的成年患者(年龄≥18 岁)。使用卡方检验和 Wilcoxon 秩和检验比较 gcGBM 和 GBM 队列的特征。采用 Kaplan-Meier 统计、单变量和多变量 Cox 回归以及倾向评分匹配评估患者、肿瘤和治疗因素与生存结果之间的关联。相关性分析用于评估 gcGBM 治疗的历史趋势。里程碑分析允许考虑无永生时间偏倚。
共确定了 683 例 gcGBM 患者。与 GBM 患者相比,gcGBM 患者的生存时间更长(从里程碑开始的 15.5 个月 vs. 11.7 个月;P<0.001)。高龄(P<0.001)与生存时间更差相关,而女性(P=0.023)和中等收入(>63,000 美元)的患者更倾向于获得更好的结局(P=0.004)。接受三联疗法(活检和/或手术、放疗和化疗)的患者与仅接受活检和/或手术或活检和/或手术加放疗而未接受全身治疗的患者相比,生存结局更好(中位生存时间:17.55 个月 vs. 6.68 个月;P<0.001)。
gcGBM 的预后优于 GBM,应积极采用三联疗法治疗。需要进行前瞻性 gcGBM 研究以更好地确定 gcGBM 的治疗结局。