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首页> 外文期刊>Journal of oncology >Antiangiogenic Therapy for Patients with Recurrent and Newly Diagnosed Malignant Gliomas
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Antiangiogenic Therapy for Patients with Recurrent and Newly Diagnosed Malignant Gliomas

机译:复发性和新诊断出的恶性胶质瘤患者的抗血管生成治疗

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摘要

Malignant gliomas have a poor prognosis despite advances in diagnosis and therapy. Although postoperative temozolomide and radiotherapy improve overall survival in glioblastoma patients, most patients experience a recurrence. The prognosis of recurrent malignant gliomas is dismal, and more effective therapeutic strategies are clearly needed. Antiangiogenesis is currently considered an attractive targeting therapy for malignant gliomas due to its important role in tumor growth. Clinical trials using bevacizumab have been performed for recurrent glioblastoma, and these studies have shown promising response rates along with progression-free survival. Based on the encouraging results, bevacizumab was approved by the FDA for the treatment of recurrent glioblastoma. In addition, bevacizumab has shown to be effective for recurrent anaplastic gliomas. Large phase III studies are currently ongoing to demonstrate the efficacy and safety of the addition of bevacizumab to temozolomide and radiotherapy for newly diagnosed glioblastoma. In contrast, several other antiangiogenic drugs have also been used in clinical trials. However, previous studies have not shown whether antiangiogenesis improves the overall survival of malignant gliomas. Specific severe side effects, difficult assessment of response, and lack of rational predictive markers are challenging problems. Further studies are warranted to establish the optimized antiangiogenesis therapy for malignant gliomas.
机译:尽管诊断和治疗有所进步,但恶性神经胶质瘤的预后较差。尽管术后替莫唑胺和放疗可改善胶质母细胞瘤患者的总体生存率,但大多数患者会复发。复发性恶性神经胶质瘤的预后令人沮丧,显然需要更有效的治疗策略。由于其在肿瘤生长中的重要作用,抗血管生成目前被认为是针对恶性神经胶质瘤的有吸引力的靶向疗法。已经针对复发性胶质母细胞瘤进行了使用贝伐单抗的临床试验,这些研究显示出有希望的缓解率以及无进展生存期。基于令人鼓舞的结果,贝伐单抗被FDA批准用于治疗复发性胶质母细胞瘤。此外,贝伐单抗已显示对复发性间变性神经胶质瘤有效。目前正在进行大规模的III期研究,以证明将贝伐单抗添加到替莫唑胺和放疗中对新诊断的胶质母细胞瘤的有效性和安全性。相反,其他几种抗血管生成药物也已用于临床试验。但是,先前的研究尚未显示抗血管生成是否能改善恶性神经胶质瘤的整体存活率。具体的严重副作用,对反应的评估困难以及缺乏合理的预测指标是具有挑战性的问题。有必要进行进一步的研究以建立针对恶性神经胶质瘤的最佳抗血管生成治疗。

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