Effect of Vascular Endothelial Growth Factor Blockers on Aqueous Humor Dynamics
Study Details
Study Description
Brief Summary
The objective of this research is to determine the effects of anti-VEGF drugs (bevacizumab, ranibizumab or aflibercept) on aqueous humor dynamics (AHD) in patients with retinal vascular disease. The underlying hypothesis is that anti-VEGF drugs increase intraocular pressure (IOP) by increasing aqueous inflow, decreasing uveoscleral outflow or both. The specific aim is to evaluate the changes produced in AHD after 1 baseline and a subsequent 1 monthly injection of anti VEGF agents.
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Detailed Description
Intravitreal injection of different anti-VEGF agents such as bevacizumab (Avastin, Genentech, Inc., South San Francisco, CA, USA) ranibizumab (Lucentis; Genentech, Inc., South San Francisco, CA, USA) and aflibercept (Eylea, Regeneron, Tarrytown, NY, USA) has been a widely common practice for treatment of choroidal neovascularization and retinal vascular diseases [1]. Several ocular and systemic adverse events have been reported with the use of anti-VEGF agents [7]. Elevation of intraocular pressure (IOP) is a serious ocular adverse event that may be associated with intravitreal injection of anti-VEGF agents. IOP elevation with anti-VEGF injection may have variable presentation ranging from acute transient post injection elevation to the development of persistent IOP elevation that mandates pressure lowering therapy[8].
Patients with previously existing glaucoma may have a higher rate of persistent IOP elevation associated with intravitreal injection of anti-VEGF agents. Good et al, reported the rate of persistent IOP elevation after intravitreal anti-VEGF to be 33% in glaucoma patients versus 3.1% in eyes without previous diagnosis of glaucoma [9]. Tseng et al, reported 25 eyes with sustained elevation of IOP after serial intravitreal injections of anti-VEGF agents (mean = 20injections). All the 25 eyes were normotensive prior to the study and 23 of them were not previously diagnosed with glaucoma[10].
Multicenter clinical trials that studied the intravitreal injection of anti-VEGF agents, such as MARINA and ANCHOR for ranibizumab, VISION for pegaptanib and PACORES for bevacizumab, did not show sustained IOP elevation with the intravitreal injection of the study agents [12-15]. However, a subgroup analysis of the data of MARINA and ANCHOR trials showed at least 6 mm Hg increase of IOP from baseline in 2.1% of eyes in MARINA trial and 3.6% of eyes in ANCHOR trial [16]. A retrospective chart review of 207 patients over a 6-months follow up period after serial intravitreal injections of anti-VEGF reported an IOP elevation greater than 5 mm Hg in 2 consecutive visits compared to baseline in 11.6% of the treated eyes versus 5.3% in control eyes [17].
The pathophysiology of the reported IOP elevation associated with intravitreal injection of anti-VEGF is unknown. Anti-VEGF compounds might increase aqueous humor inflow by the breakdown of the blood-aqueous barrier or reduce uveoscleral outflow by the ciliary body vasculature. These potential changes could translate into elevated IOP and glaucoma.
Study Design
Outcome Measures
Primary Outcome Measures
- Uveoscleral outflow changes [1-2 months]
The uveoscleral outflow changes will be assess at baseline prior to any anti-VEGF treatment and after the 3rd intravitreal treatment has been done.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Subjects must be at least 19 years of age and older
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Ability to give informed consent and attend the study visits
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Patients with established diagnosis of retinal vascular diseases (diabetic macular edema, neovascular macular degeneration,presumed ocular histoplasmosis syndrome, high myopia) who require intravitreal injection of anti-VEGF drugs such as bevacizumab,ranibizumab or aflibercept and are likely to need three monthly doses.
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Patients who have not received intravitreal injections within 3 months of study entry
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No previous established diagnosis of glaucoma and consequently no previous history of Argon Laser Trabeculoplasty (ALT) or Selective Laser Trabeculoplasty (SLT).
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No previous history of ocular surgery
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Patients who are not planning on and are unlikely to require an elective ocular surgical or laser procedure within the study duration
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Open angle of the anterior chamber on clinical examination
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Ability to cooperate for aqueous humor dynamic studies
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Contact lenses removed prior to topical fluorescein instillation, and not used until the end of each fluorophotometry session
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Able to participate on site over the multi-visit study period
Exclusion Criteria:
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Age less than 18 years of age
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Women who are pregnant or nursing
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Ocular hypertension or glaucoma
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Narrow angle with complete or partial closure (gonioscopy angle <2)
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Any previous surgical or laser procedures
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Secondary glaucoma including pigmentary, exfoliative, uveitic and traumatic glaucomas
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Any active neovascularization of the iris, angle, disc or retina
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Diagnosis of retinal arterial or vein occlusion
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Chronic or recurrent inflammatory eye disease
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Ocular trauma within the past 6 months
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Ocular infection or ocular inflammation in the past 2 months
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Any abnormality preventing reliable fluorophotometry of either eye,such as corneal scarring or severe dry eye that results in punctuate fluorescein staining of the cornea
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Intraocular surgery within 6 months
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Serious hypersensitivity to any components of the study medications or risk from treatment with glaucoma medications, such as severe asthma or emphysema.
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Use of any glucocorticoid by any route. Subject must be washed out of the glucocorticoid for at least 2 weeks before study entry.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Nebraska Medical Center, Truhlsen Eye Institute | Omaha | Nebraska | United States | 68105 |
| 2 | University of Nebraska Medical Center, Department of Ophthalmology and Visual Sciences | Omaha | Nebraska | United States | 68198-5540 |
Sponsors and Collaborators
- University of Nebraska
Investigators
- Principal Investigator: Vikas Gulati, MD, UNMC Department of Ophthalmology and Visual Sciences
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 583-13-FB