Boaro Alessandro, Kavouridis Vasileios K, Siddi Francesca, Mezzalira Elisabetta, Harary Maya, Iorgulescu J Bryan, Reardon David A, Smith Timothy R
Computational Neuroscience Outcomes Center, Department of Neurosurgery, Brigham and Women's Hospital, 60 Fenwood Rd., Boston, MA, , 02115, USA.
Harvard Medical School, Boston, MA, USA.
Acta Neurochir (Wien). 2021 Jul;163(7):1883-1894. doi: 10.1007/s00701-021-04844-w. Epub 2021 Apr 19.
Butterfly glioblastomas (bGBMs) are grade IV gliomas that infiltrate the corpus callosum and spread to bilateral cerebral hemispheres. Due to the rarity of cases, there is a dearth of information in existing literature. Herein, we evaluate clinical and genetic characteristics, associated predictors, and survival outcomes in an institutional series and compare them to a national cohort.
We identified all adult patients with bGBM treated at Brigham & Women's Hospital (2008-2018). The National Cancer Database (NCDB) was also queried for bGBM patients. Survival was analyzed with Kaplan-Meier methods, and Cox models were built to assess for predictive factors.
Of 993 glioblastoma patients, 62 cases (6.2%) of bGBM were identified. Craniotomy for resection was attempted in 26 patients (41.9%), with a median volumetric extent of resection (vEOR) of 72.3% (95% confidence interval [95%CI] 58.3-82.1). The IDH1 R132H mutation was detected in two patients (3.2%), and MGMT promoter was methylated in 55.5% of the assessed cases. In multivariable regression, factors predictive of longer OS were increased vEOR, MGMT promoter methylation, and receipt of adjuvant therapy. Median OS for the resected cases was 11.5 months (95%CI 7.7-18.8) vs. 6.3 (95%CI 5.1-8.9) for the biopsied. Of 21,353 GBMs, 719 (3.37%) bGBM patients were identified in the NCDB. Resection was more likely to be pursued in recent years, and GTR was independently associated with prolonged OS (p < 0.01).
Surgical resection followed by adjuvant chemoradiation is associated with significant survival gains and should be pursued in carefully selected bGBM patients.
蝶形胶质母细胞瘤(bGBM)是IV级胶质瘤,可浸润胼胝体并扩散至双侧大脑半球。由于病例罕见,现有文献资料匮乏。在此,我们评估了一个机构系列中的临床和基因特征、相关预测因素及生存结果,并将其与全国队列进行比较。
我们确定了在布莱根妇女医院接受治疗的所有成年bGBM患者(2008 - 2018年)。还对国家癌症数据库(NCDB)中的bGBM患者进行了查询。采用Kaplan - Meier方法分析生存情况,并构建Cox模型评估预测因素。
在993例胶质母细胞瘤患者中,确诊62例(6.2%)bGBM。26例患者(41.9%)尝试进行开颅切除术,切除体积中位数(vEOR)为72.3%(95%置信区间[95%CI]58.3 - 82.1)。两名患者(3.2%)检测到IDH1 R132H突变,55.5%的评估病例中MGMT启动子发生甲基化。在多变量回归中,预测总生存期较长的因素包括vEOR增加、MGMT启动子甲基化和接受辅助治疗。切除病例的中位总生存期为11.5个月(95%CI 7.7 - 18.8),而活检病例为6.3个月(95%CI 5.1 - 8.9)。在21,353例胶质母细胞瘤中,国家癌症数据库中确诊719例(3.37%)bGBM患者。近年来更倾向于进行切除术,而大体肿瘤切除(GTR)与总生存期延长独立相关(p < 0.01)。
手术切除后进行辅助放化疗可显著提高生存率,应在精心挑选的bGBM患者中实施。