Identification of Patients With Glioblastoma Who May Benefit from Hypofractionated Radiotherapy

被引:6
|
作者
Zemskova, Oksana [1 ,2 ]
Yu, Nathan Y. [3 ]
Trillenberg, Peter [4 ]
Bonsanto, Matteo M. [5 ]
Leppert, Jan [5 ]
Rades, Dirk [1 ,6 ]
机构
[1] Univ Lubeck, Dept Radiat Oncol, Lubeck, Germany
[2] Romodanov Neurosurg Inst, Dept Radioneurosurg, Kiev, Ukraine
[3] Mayo Clin, Dept Radiat Oncol, Phoenix, AZ USA
[4] Univ Lubeck, Dept Neurol, Lubeck, Germany
[5] Univ Lubeck, Dept Neurosurg, Lubeck, Germany
[6] Univ Lubeck, Dept Radiat Oncol, Ratzeburger 160, D-23562 Lubeck, Germany
关键词
Glioblastoma; radiation therapy; hypofractionation; overall survival; local control; prognostic score; NEWLY-DIAGNOSED GLIOBLASTOMA; RADIATION-THERAPY; PROGNOSTIC-FACTORS; SURVIVAL; BEVACIZUMAB; MULTIFORME;
D O I
10.21873/anticanres.16439
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Standard radiotherapy (RT) for glioblastoma lasts 6 weeks. We aimed to identify patients who would benefit from a hypofractionated approach. Patients and Methods: In 167 patients receiving standard fractionation, 10 factors were analyzed for local control (LC) and overall survival (OS). A survival score was developed and compared to a previous instrument. Results: On multivariate analysis, better LC was significantly associated with the presence of only one lesion and O6- methylguanine-DNA methyltransferase (MGMT) promoter methylation. Better OS was associated with one lesion, better performance status, MGMT promoter methylation, and receipt of chemotherapy. Lesion diameter <= 40 mm and upfront resection were associated with improved OS on univariate analyses. Based on assigning scores to these six factors, three groups, with 32-35, 36-44 and 45-48 points, were designed with 12-month OS-rates of 0%, 56%, and 92%, respectively. Accuracy in predicting death within 12 months and survival >= 12 months was 100% and 92%, respectively, versus 67% and 83% with the previous scoring system. Conclusion: A new survival score with higher accuracy was developed for patients with glioblastoma. Our model can be utilized to individualize RT dose-fractionation recommendations for glioblastoma.
引用
收藏
页码:2725 / 2732
页数:8
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