With the introduction of anti-VEGF therapy, clinicians have argued
whether pharmacotherapy or laser panretinal photocoagulation (PRP)
deserves consideration as the first-line treatment for proliferative
diabetic retinopathy (PDR).
Since the results of the Diabetic Retinopathy Study were reported in
1981, PRP has been the gold standard treatment for PDR. Then, in 2015,
anti-VEGF therapy with intravitreal ranibizumab (Lucentis, Genentech)
emerged as a new option, based on findings from Diabetic Retinopathy
Clinical Research Network (DRCR.net) Protocol S.
In that prospective, randomized study, the primary outcome analysis of
mean change in visual acuity (VA) from baseline showed ranibizumab 0.5
mg was non-inferior to PRP at 2 years. Statistically, significant
differences favoring ranibizumab were found in analyses of VA area under
the curve over the course of the study, visual field sensitivity loss,
vitrectomy rate, and incidence of diabetic macular edema (DME).
Debating the roles of PRP and anti-VEGF therapy for PDR, Judy E. Kim,
MD, professor of ophthalmology, Medical College of Wisconsin, Milwaukee,
named the level 1 evidence from Protocol S as one of five reasons why
retina specialists should consider choosing pharmacotherapy.
source: ophthalmologytimes
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