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伊立替康联合贝伐珠单抗治疗复发性多形性胶质母细胞瘤。

Irinotecan and bevacizumab in recurrent glioblastoma multiforme.

机构信息

Copenhagen University Hospital, The Finsencenter, Department of Oncology, Blegdamsvej 9, DK 2100 Copenhagen, Denmark.

出版信息

Expert Opin Pharmacother. 2011 Apr;12(5):825-33. doi: 10.1517/14656566.2011.566558. Epub 2011 Mar 9.

Abstract

INTRODUCTION

Glioblastoma multiforme (GBM) is the most common high grade primary brain tumor in adults. Despite significant advances in treatment, the prognosis remains poor. Bevacizumab (BVZ) and irinotecan (CPT-11) are currently being investigated in the treatment of GBM patients. Although treatment with BVZ and irinotecan provides impressive response rates (RR), it is still uncertain if this treatment translates into improved clinical benefit in GBM patients.

AREAS COVERED

This review discusses the clinical efficacy, safety and difficulties regarding response evaluation when treating with BVZ and CPT-11 in recurrent GBM. Particular attention is placed on the literature and a discussion on whether treatment with BVZ and CPT-11 improves clinical outcome. Antiangiogenic treatment has led to difficulties when evaluating objective response by the conventional MacDonald criteria. In the present paper the authors discuss selected key aspects of this treatment modality. A literature search was performed using PubMed in February 2011.

EXPERT OPINION

BVZ + irinotecan leads to high RR and to an increased 6-month progression-free survival. However, no improvement in median overall survival has been observed compared with conventional chemotherapy. Nevertheless, the GBM patients who respond to treatment with BVZ and irinotecan have survived significantly longer than non-responders, indicating that it could be beneficial for a selection of patients to receive this treatment.

摘要

简介

多形性胶质母细胞瘤(GBM)是成人中最常见的高级原发性脑肿瘤。尽管在治疗方面取得了重大进展,但预后仍然很差。贝伐单抗(BVZ)和伊立替康(CPT-11)目前正在用于治疗 GBM 患者。尽管使用 BVZ 和伊立替康治疗可提供令人印象深刻的缓解率(RR),但仍不确定这种治疗是否能改善 GBM 患者的临床获益。

涵盖领域

本文讨论了在复发性 GBM 中使用 BVZ 和 CPT-11 治疗时的临床疗效、安全性和反应评估困难。特别关注文献,并讨论了使用 BVZ 和 CPT-11 是否改善了临床结局。抗血管生成治疗在使用传统的 MacDonald 标准评估客观反应时带来了困难。在本文中,作者讨论了这种治疗方式的一些关键方面。2011 年 2 月在 PubMed 上进行了文献检索。

专家意见

BVZ + 伊立替康可导致高 RR 和 6 个月无进展生存率增加。然而,与常规化疗相比,中位总生存期没有改善。然而,对 BVZ 和伊立替康治疗有反应的 GBM 患者的存活时间明显长于无反应者,这表明对一部分患者来说,接受这种治疗可能是有益的。

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