Changes in retinal neovascularization after pegaptanib (Macugen) therapy in diabetic individuals

被引:180
作者
Adamis, AP
Altaweel, M
Bressler, NM
Cunningham, ET
Davis, MD
Goldbaum, M
Gonzales, C
Guyer, DR
Katz, B
Patel, M
机构
[1] Baltimore, MD 21205-2002
[2] Madison, WI 53705
[3] University of Wisconsin, Madison, WI
关键词
D O I
10.1016/j.ophtha.2005.10.012
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: To study effects of intravitreal pegaptanib (Macugen) on retinal neovascularization. Design: Retrospective analysis of a randomized clinical trial. Participants, Intervention, and Main Outcome Measures: Individuals with retinal neovascularization identified from a multicenter, randomized, controlled trial evaluating pegaptanib for treatment of diabetic macular edema, with a best-corrected visual acuity letter score between 68 and 25 (approximate Snellen equivalent between 20/50 and 20/320) and receiving a sham injection or intravitreal pegaptanib (0.3 mg, 1 mg, 3 mg) administered at study entry, week 6, and week 12, with additional injections and/or focal photocoagulation as needed during the ensuing 18 weeks, up to a maximum of 6 pegaptanib/sham therapies, were evaluated. Scatter panretinal photocoagulation before study enrollment was permitted, but not within 6 months of randomization and study entry. Changes in retinal neovascularization were assessed on fundus photographs and fluorescein angiograms graded at a reading center in a masked fashion. Results: Of 172 participants, 19 had retinal neovascularization in the study eye at baseline. Excluding 1 who had scatter photocoagulation 13 days before randomization and 2 with no follow-up photographs, 1 of the remaining 16 subjects had panretinal photocoagulation during study follow-up. Of these 16 subjects, 8 of 13 (62%) in a pegaptanib treatment group (including the one receiving panretinal photocoagulation), 0 of 3 in the sham group, and 0 of 4 fellow (nonstudy) eyes showed either regression of neovascularization on funclus photographs or regression or absence of fluorescein leakage from neovascularization (or both) at 36 weeks. In 3 of 8 with regression, neovascularization progressed at week 52 after cessation of pegaptanib at week 30. Conclusions: Most subjects with retinal neovascularization at baseline assigned to pegaptanib showed regression of neovascularization by week 36. These findings suggest a direct effect of pegaptanib upon retinal neovascularization in patients with diabetes mellitus.
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页码:23 / 28
页数:6
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