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贝伐单抗用于治疗年龄相关性黄斑变性的超说明书用药:证据是什么?

Off-label use of bevacizumab for the treatment of age-related macular degeneration: what is the evidence?

作者信息

Ziemssen Focke, Grisanti Salvatore, Bartz-Schmidt Karl Ulrich, Spitzer Martin S

机构信息

University Eye Hospital, Centre for Ophthalmology, Eberhard-Karls University of Tuebingen, Tuebingen, Germany.

出版信息

Drugs Aging. 2009;26(4):295-320. doi: 10.2165/00002512-200926040-00002.

Abstract

There is an active and controversial debate about the role of intravitreal bevacizumab versus approved drugs in the treatment of neovascular age-related macular degeneration (AMD). Because bevacizumab was available prior to the launch of ranibizumab, off-label use of the former became widespread and the cancer drug bevacizumab is the most commonly used medication in ophthalmology nowadays. This review considers every publication identified in MEDLINE using the keywords 'bevacizumab' and 'Avastin' between 1 June 2005 and 31 July 2008. The search identified 511 papers that were evaluated. In 33 studies, there was consistent and clear evidence for the efficacy of bevacizumab in neovascular AMD. However, the highest grade studies (three prospective, randomized, controlled trials) did not attain better than grade 2b level of evidence, and objective evaluation of the benefit of bevacizumab relative to representative controls was therefore not possible. Certainly, the available evidence is inferior to that obtained from the approval studies of ranibizumab and this should influence treatment selection and guidance of patients. These considerations indicate that important quality criteria need to be included in future studies to ensure more meaningful conclusions can be drawn. These include clearly defined inclusion criteria, information about the recruitment procedure (including data on withdrawals, excluded patients, concealed treatment allocation, use of intention-to-treat analyses and blinded assessment procedures). Although preclinical studies have almost exclusively found bevacizumab to be safe, the design utilized in clinical case series cannot rule out a possible increase in adverse events, which already show a high spontaneous incidence in elderly AMD patients. The superior evidence level for ranibizumab and the limited safety data for bevacizumab must be taken into consideration when evaluating the costs that a healthcare system is willing to spend. However, the superior grade of evidence for ranibizumab should not be confused with the (still missing) evidence for superior efficacy. The results of ongoing randomized, controlled, comparative trials will provide further data on the efficacy and cost effectiveness of bevacizumab and ranibizumab in the treatment of AMD. In the meantime, patients should be informed about the alternatives, the price differences and the restricted liability issue when off-label use of bevacizumab is offered.

摘要

关于玻璃体内注射贝伐单抗与已获批药物在治疗新生血管性年龄相关性黄斑变性(AMD)中的作用,存在着一场活跃且颇具争议的辩论。由于贝伐单抗在雷珠单抗上市之前就已存在,前者的非标签使用变得广泛,且这种癌症药物贝伐单抗如今是眼科最常用的药物。本综述考量了2005年6月1日至2008年7月31日期间在MEDLINE中使用关键词“贝伐单抗”和“阿瓦斯汀”检索到的每一篇出版物。该检索共识别出511篇有待评估的论文。在33项研究中,有一致且明确的证据表明贝伐单抗对新生血管性AMD有效。然而,最高等级的研究(三项前瞻性、随机、对照试验)未达到高于2b级别的证据水平,因此无法对贝伐单抗相对于代表性对照的益处进行客观评估。当然,现有证据不如从雷珠单抗的获批研究中获得的证据,这应会影响治疗选择及对患者的指导。这些考量表明,未来研究需要纳入重要的质量标准,以确保能得出更有意义的结论。这些标准包括明确界定的纳入标准、关于招募程序的信息(包括退出数据、排除患者的数据、隐藏治疗分配、意向性分析的使用及盲法评估程序)。尽管临床前研究几乎无一例外地发现贝伐单抗是安全的,但临床病例系列中采用的设计无法排除不良事件可能增加的情况,而在老年AMD患者中不良事件的自发发生率本就很高。在评估医疗系统愿意投入的成本时,必须考虑雷珠单抗更高的证据水平以及贝伐单抗有限的安全性数据。然而雷珠单抗更高等级的证据不应与(仍缺失的)更高疗效的证据相混淆。正在进行的随机、对照、比较试验的结果将提供关于贝伐单抗和雷珠单抗治疗AMD的疗效及成本效益的进一步数据。与此同时,当提供贝伐单抗的非标签使用时,应告知患者相关替代方案、价格差异及责任受限问题。

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