Pharmacotherapies for the treatment of glioblastoma - current evidence and perspectives

被引:23
作者
Seystahl, Katharina [1 ]
Gramatzki, Dorothee
Roth, Patrick
Weller, Michael
机构
[1] Univ Zurich Hosp, Dept Neurol, Frauenklinikstr 26, CH-8091 Zurich, Switzerland
关键词
Glioblastoma; temozolomide; bevacizumab; clinical trial; immunotherapy; NEWLY-DIAGNOSED GLIOBLASTOMA; RANDOMIZED PHASE-III; SINGLE-AGENT BEVACIZUMAB; DOSE-DENSE TEMOZOLOMIDE; RECURRENT GLIOBLASTOMA; OPEN-LABEL; RADIATION-THERAPY; ADJUVANT TEMOZOLOMIDE; STANDARD TREATMENT; UNITED-STATES;
D O I
10.1080/14656566.2016.1176146
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Glioblastoma, the most common malignant brain tumor, exhibits a poor prognosis with little therapeutic progress in the last decade. Novel treatment strategies beyond the established standard of care with temozolomide-based radiotherapy are urgently needed. Areas covered: We reviewed the literature on glioblastoma with a focus on phase III trials for pharmacotherapies and/or innovative concepts until December 2015. Expert opinion: In the last decade, phase III trials on novel compounds largely failed to introduce efficacious pharmacotherapies beyond temozolomide in glioblastoma. So far, inhibition of angiogenesis by compounds such as bevacizumab, cediranib, enzastaurin or cilengitide as well as alternative dosing schedules of temozolomide did not prolong survival, neither at primary diagnosis nor at recurrent disease. Promising strategies of pharmacotherapy currently under evaluation represent targeting epidermal growth factor receptor (EGFR) with biomarker-stratified patient populations and immunotherapeutic concepts including checkpoint inhibition and vaccination. The clinical role of the medical device delivering 'tumor-treating fields' in newly diagnosed glioblastoma which prolonged overall survival in a phase III study has remained controversial. After failure of several phase III trials with previously promising agents, improvement of concepts and novel compounds are urgently needed to expand the still limited therapeutic options for the treatment of glioblastoma.
引用
收藏
页码:1259 / 1270
页数:12
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