Molecularly Targeted Clinical Trials

被引:6
作者
Smith-Cohn, Matthew A. [1 ,2 ]
Celiku, Orieta [3 ]
Gilbert, Mark R. [3 ]
机构
[1] NCI, Neurooncol Branch, NIH, 37 Convent Dr,Bldg 37,Room 1016, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, Dept Neurol, Sch Med, Baltimore, MD 21287 USA
[3] NCI, Neurooncol Branch, NIH, 37 Convent Dr,Bldg 37,Room 1142, Bethesda, MD 20892 USA
关键词
Glioblastoma; Heterogenicity; Targeted therapy; Blood-brain barrier; Synthetic lethality; SYNTHETIC LETHAL INTERACTIONS; MGMT PROMOTER METHYLATION; CENTRAL-NERVOUS-SYSTEM; PREDICTIVE-VALUE; PRIMARY BRAIN; CANCER; TUMORS; GLIOBLASTOMA; TEMOZOLOMIDE; CHEMOTHERAPY;
D O I
10.1016/j.nec.2020.12.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glioblastoma remains incurable despite advances in surgery, radiation, and chemotherapy, underscoring the need for new therapies. The genetic heterogenicity, presence of redundant molecular pathways, and the blood-brain barrier have limited the applicability of molecularly targeted agents. The therapeutic benefit seen with a small subset of patients suggests, however, that patient selection is critical. Recent investigations show that molecularly targeted synthetic lethality is a promising complementary approach. The article provides an overview of the challenges of molecularly targeted therapy in adults with glioblastoma, including current trials and future therapeutic directions. © 2020
引用
收藏
页码:191 / 210
页数:20
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