National Cancer Institute, Neuro-Oncology Branch, National Institutes of Health, Bethesda, Maryland, USA.
Onco Targets Ther. 2010 Jun 24;3:27-38. doi: 10.2147/ott.s5307.
Glioblastoma multiforme (GBM) is the most common malignant primary brain tumor in adults and carries the poorest prognosis. Despite recent progress in molecular biology, neuro-imaging and neuro-surgical care, the management of patients with GBM continues to harbor significant challenges. Survival after diagnosis is poor even with the most aggressive approach using multimodality therapy. Although the etiology of malignant gliomas is not known, the dependency of tumor growth on angiogenesis has identified this pathway as a promising therapeutic target. Bevacizumab was the first antiangiogenic therapy approved for use in cancer and received accelerated Food and Drug Administration approval for the treatment of recurrent GBM in 2009, the first new drug for this disease in over a decade. This review describes the rationale behind the treatment of GBM with bevacizumab. The pharmacology, efficacy, safety and tolerability of bevacizumab will also be reviewed.
多形性胶质母细胞瘤(GBM)是成年人中最常见的恶性原发性脑肿瘤,预后最差。尽管在分子生物学、神经影像学和神经外科护理方面取得了最近的进展,但胶质母细胞瘤患者的管理仍然存在重大挑战。即使采用最积极的多模式治疗方法,诊断后的生存率仍然很差。尽管恶性神经胶质瘤的病因尚不清楚,但肿瘤生长对血管生成的依赖性已将该途径确定为有前途的治疗靶点。贝伐单抗是第一种获准用于癌症的抗血管生成疗法,并于 2009 年获得美国食品和药物管理局加速批准用于复发性 GBM 的治疗,这是十多年来该疾病的第一种新药。本文描述了用贝伐单抗治疗 GBM 的基本原理。还将回顾贝伐单抗的药理学、疗效、安全性和耐受性。