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血管生成作为恶性胶质瘤的治疗靶点。

Angiogenesis as a therapeutic target in malignant gliomas.

作者信息

Chi Andrew S, Sorensen A Gregory, Jain Rakesh K, Batchelor Tracy T

机构信息

Department of Neurology, Division of Hematology and Oncology, Massachusetts General Hospital Cancer Center, Boston, Massachusetts 02114, USA.

出版信息

Oncologist. 2009 Jun;14(6):621-36. doi: 10.1634/theoncologist.2008-0272. Epub 2009 Jun 1.

Abstract

Currently, adult glioblastoma (GBM) patients have poor outcomes with conventional cytotoxic treatments. Because GBMs are highly angiogenic tumors, inhibitors that target tumor vasculature are considered promising therapeutic agents in these patients. Encouraging efficacy and tolerability in preliminary clinical trials suggest that targeting angiogenesis may be an effective therapeutic strategy in GBM patients. However, the survival benefits observed to date in uncontrolled trials of antiangiogenic agents have been modest, and several obstacles have limited their effectiveness. This article reviews the rationale for antiangiogenic agents in GBM, their potential mechanisms of action, and their clinical development in GBM patients. Although challenges remain with this approach, ongoing studies may improve upon the promising initial benefits already observed in GBM patients.

摘要

目前,成胶质细胞瘤(GBM)成年患者接受传统细胞毒性治疗的预后较差。由于GBM是高度血管生成性肿瘤,靶向肿瘤脉管系统的抑制剂被认为是这些患者有前景的治疗药物。初步临床试验中令人鼓舞的疗效和耐受性表明,靶向血管生成可能是GBM患者的一种有效治疗策略。然而,迄今为止在抗血管生成药物的非对照试验中观察到的生存获益不大,并且有几个障碍限制了它们的有效性。本文综述了GBM中抗血管生成药物的理论依据、其潜在作用机制以及在GBM患者中的临床研发情况。尽管这种方法仍存在挑战,但正在进行的研究可能会改善GBM患者已经观察到的有前景的初步获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8309/4790121/d502357d7942/nihms765709f1.jpg

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