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眼部血管内皮生长因子的长期抑制:失败、成功与未来可能性

Extended Duration Vascular Endothelial Growth Factor Inhibition in the Eye: Failures, Successes, and Future Possibilities.

作者信息

Stewart Michael W

机构信息

Department of Ophthalmology, Mayo Clinic School of Medicine, 4500 San Pablo Rd., Jacksonville, FL 32224, USA.

出版信息

Pharmaceutics. 2018 Jan 27;10(1):21. doi: 10.3390/pharmaceutics10010021.

Abstract

Vascular endothelial growth factor (VEGF) plays a pivotal role in the development of neovascularization and edema from several common chorioretinal vascular conditions. The intravitreally injected drugs (aflibercept, bevacizumab, conbercept, pegaptanib, and ranibizumab) used to treat these conditions improve the visual acuity and macular morphology in most patients. Monthly or bimonthly injections were administered in the phase III pivotal trials but physicians usually individualize therapy with (PRN) or treat and extend regimens. Despite these lower frequency treatment regimens, frequent injections and clinic visits are still needed to produce satisfactory outcomes. Newly developed drugs and refillable reservoirs with favorable pharmacokinetic profiles may extend durations of action and require fewer office visits. However, we have learned from previous experiences that the longer durations of action seen in strategically designed phase III trials often do not translate to less frequent injections in real-life clinical practice. Unfortunately, long-acting therapies that produce soluble VEGF receptors (encapsulated cell technology and adenovirus injected DNA) have failed in phase II trials. The development of longer duration therapies remains a difficult and frustrating process, and frequent drug injections are likely to remain the standard-of-care for years to come.

摘要

血管内皮生长因子(VEGF)在几种常见的脉络膜视网膜血管疾病的新生血管形成和水肿发展过程中起关键作用。用于治疗这些疾病的玻璃体内注射药物(阿柏西普、贝伐单抗、康柏西普、培加尼布和雷珠单抗)在大多数患者中可改善视力和黄斑形态。在III期关键试验中采用每月或每两个月注射一次,但医生通常根据需要(PRN)个体化治疗或采用治疗并延长方案。尽管采用了这些较低频率的治疗方案,但仍需要频繁注射和门诊就诊才能取得满意的疗效。新开发的具有良好药代动力学特征的药物和可再填充的储库可能会延长作用持续时间并减少门诊次数。然而,我们从以往的经验中了解到,在精心设计的III期试验中观察到的较长作用持续时间在实际临床实践中往往并不能转化为更少的注射频率。不幸的是,产生可溶性VEGF受体的长效疗法(封装细胞技术和腺病毒注射DNA)在II期试验中失败了。开发更长作用持续时间的疗法仍然是一个困难且令人沮丧的过程,频繁的药物注射可能在未来几年仍将是标准治疗方法。

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本文引用的文献

1
Characterization of liposomal carriers for the trans-scleral transport of Ranibizumab.
Sci Rep. 2017 Dec 1;7(1):16803. doi: 10.1038/s41598-017-16791-7.
2
Intravitreal Ziv-Aflibercept: Clinical Effects and Economic Impact.
Asia Pac J Ophthalmol (Phila). 2017 Nov-Dec;6(6):561-568. doi: 10.22608/APO.2017263. Epub 2017 Oct 3.
3
Brolucizumab Versus Aflibercept in Participants with Neovascular Age-Related Macular Degeneration: A Randomized Trial.
Ophthalmology. 2017 Sep;124(9):1296-1304. doi: 10.1016/j.ophtha.2017.03.057. Epub 2017 May 24.
4
One-Year Feasibility Study of Replenish MicroPump for Intravitreal Drug Delivery: A Pilot Study.
Transl Vis Sci Technol. 2014 Jul 1;3(4):8. doi: 10.1167/tvst.3.3.8. eCollection 2014 May.
5
Aflibercept, bevacizumab, or ranibizumab for diabetic macular edema.
N Engl J Med. 2015 Mar 26;372(13):1193-203. doi: 10.1056/NEJMoa1414264. Epub 2015 Feb 18.
6
Implantable MicroPump for Drug Delivery in Patients with Diabetic Macular Edema.
Transl Vis Sci Technol. 2014 Dec 1;3(6):5. doi: 10.1167/tvst.3.6.5. eCollection 2014 Oct.
7
Intravitreal aflibercept injection for neovascular age-related macular degeneration: ninety-six-week results of the VIEW studies.
Ophthalmology. 2014 Jan;121(1):193-201. doi: 10.1016/j.ophtha.2013.08.011. Epub 2013 Sep 29.
8
Treatment of diabetic macular edema with a designed ankyrin repeat protein that binds vascular endothelial growth factor: a phase I/II study.
Am J Ophthalmol. 2013 Apr;155(4):697-704, 704.e1-2. doi: 10.1016/j.ajo.2012.09.032. Epub 2012 Dec 4.
9
Intravitreal aflibercept (VEGF trap-eye) in wet age-related macular degeneration.
Ophthalmology. 2012 Dec;119(12):2537-48. doi: 10.1016/j.ophtha.2012.09.006. Epub 2012 Oct 17.

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