Clinical Drug Experience Knowledgebase

Lucentis in the Treatment of Macular Edema - A Phase II, Single Center, Randomized Study to Evaluate the Efficacy of Ranibizumab Versus Focal Laser Treatment in Subjects With Diabetic Macular Edema

Diabetic macular edema (DME) results from abnormal leakage of macromolecules into the extracellular space from microaneurysms and incompetent blood vessel walls due to small vessel damage from high blood glucose levels. Oncotic forces then allow water into the extracellular space. Abnormalities in the retinal pigment epithelium (RPE) may reduce normal outflow of fluid from the retina to the underlying choriocapillaris via the pump mechanism (Ferris et al. 1984). This leads to retinal edema in the macula with accompanying loss of vision. There is evidence suggesting that vascular endothelial growth factor (VEGF) plays a part in vessel wall permeability with subsequent retinal edema (Aiello et al. 1997).

Studies demonstrate that tight junctions in the vessel walls were shown to be regulated by VEGF and VEGF increases vascular permeability (Anticliff et al. 1999). The healthy human retina contains little or no VEGF. Hypoxia, a component of diabetic retinopathy, causes upregulation of VEGF in the retina (Vinores et al. 1997). Binding VEGF with an antibody specific for VEGF may inhibit resultant edema thus preventing and possibly reversing loss of vision.

Diabetic retinopathy is the leading cause of blindness in people aged 20-74 years, accounting for 8% of all cases of legal blindness and 12% of the newly blind (Klein 1995). A common complication of all forms of diabetes mellitus, diabetic retinopathy is present in over 2.5% of the U.S. population, or more than 5.3 million people aged 18 or older (Prevent Blindness American 2002).

Three forms of retinopathy are commonly recognized in association with all forms of diabetes mellitus: 1) non-proliferative diabetic retinopathy (NPDR), 2) proliferative diabetic retinopathy (PDR), and 3) diabetic macular edema (DME).

NPDR is characterized by ophthalmoscopically visable abnormalities that include microaneurysms, intraretinal hemorrhages, exudates, retina nerve fiber layer infarcts (cotton-wool spots), and, in more severe cases, venous beading and intraretinal microvascular abnormalities (IRMA).

Over time, NPDR may progress to more severe PDR, the hallmark of which is neovascularization on the surface of the retina, optic disc, or iris, and angle structures in the front of the eye. PDR is associated with a high risk of visual morbidity arising from vitreous hemorrhage, traction retinal detachment, and neovascular glaucoma (Diabetic Retinopathy Research Group 1979).

DME, the third form of diabetic retinopathy, is characterized by swelling of the central part of the retina that mediates high-resolution vision. DME frequently coexists with and is superimposed upon NPDR or PDR. When the area of swelling is located more than 1 disc diameter (approximately 1500 mm) away from the center of the fovea, the swelling constitutes a low threat to visual acuity and is regarded as non-clinically significant macular edema (Early Treatment Diabetic Retinopathy Study [ETDRS] Research Group 1985). Vision deteriorates when DME involves the foveal center. DME that either directly involves the fovea or is at high risk of doing so is referred to as Clinically Significant Macular Edema (CSME) (ETDRS Research Group 1985).

When the center of the fovea is involved by CSME, the DME is referred to as CSME with center involvement (CSME-CI), as opposed to CSME without center involvement (ETDRS Research Group 1987).

The natural history of untreated CSME-CI is particularly poor. The ETDRS demonstrated that over a 3-year period, 33% of subjects with CSME-CI lose >15 letters of visual acuity on the standardized ETDRS Visual Acuity Chart (Ferris et al. 1982) compared with 23% of CSME subjects without center involvement (ETDRS Research Group 1987). Such a degree of visual acuity change is equivalent to doubling of the visual angle or greater. The ETDRS did not discriminate between subtypes of diabetes mellitus.

Although laser photocoagulation in CSME-CI was shown to reduce the proportion of subjects losing > 15 letters from 33% to 13% over 3 years, 13% of subjects nevertheless continued to double their visual angle or do worse. Moreover, in subjects with CSME initially without center involvement, over 3 years, 12% lose > 15 letters despite laser treatment, presumably because edema eventually involves the center of the fovea (i.e., the subjects convert to CSME-CI). Thus, while laser is an effective tool in the treatment of CSME, there is a considerable unmet clinical need for CSME-CI.

This study is designed to compare the effectiveness of intra-vitreal Ranibizumab to current standard of care.