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Sequential combined treatment with intravitreal bevacizumab and photodynamic therapy for retinal angiomatous proliferation.

机译:序贯联合玻璃体内贝伐单抗联合光动力疗法治疗视网膜血管瘤增生。

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PURPOSE: To study visual and anatomical outcomes of sequenced combined therapy using intravitreal bevacizumab followed by photodynamic therapy (PDT) in eyes with retinal angiomatous proliferation (RAP). Safety and rate of intravitreal injections were also evaluated. METHODS: We conducted a prospective non-comparative pilot study of consecutive patients newly diagnosed with RAP. PDT guided by indocyanine green (ICG) angiography was applied 8+/-2 days after the intravitreal bevacizumab (1.25 mg) injection. At baseline and every month after the injection, best-corrected visual acuity (BCVA) measurement, complete eye examination including dynamic fluorescein and ICG angiography, and optical coherence tomography (OCT) were performed. RESULTS: In all, 21 eyes of 18 patients with RAP were enrolled. The mean age was 77 (range 65-86) years. Mean visual acuity at baseline was 0.63+/-0.25 logMAR. After treatment BCVA showed no statistically significant differences between each visit (P=0.10, ANOVA). At 9 months, the BCVA improved by three or more lines in three eyes (14%), remained stable in twelve eyes (57%), and worsened in six eyes (29%). Foveal thickness decreased significantly between baseline and all the follow-up visits (P<0.01, ANOVA). A total of 36 intravitreal injections were given during the study with a mean of 1.7 injections per eye (range 1-3 injections per eye). No ocular or systemic adverse events were reported. CONCLUSION: A possible synergistic effect may arise from the combination of intravitreal bevacizumab with PDT for the treatment of RAP. These findings also suggest a possible benefit of combo therapy in the rate of intravitreal re-injections.
机译:目的:研究在视网膜血管瘤增生(RAP)的眼睛中使用玻璃体内贝伐单抗联合光动力疗法(PDT)进行序贯联合治疗的视觉和解剖学结果。还评估了玻璃体内注射的安全性和速率。方法:我们对新诊断为RAP的连续患者进行了一项前瞻性非比较性前瞻性研究。玻璃体内注射贝伐单抗(1.25 mg)注射后8 +/- 2天,应用由吲哚菁绿(ICG)血管造影术指导的PDT。在基线和注射后的每个月,均进行最佳矫正视力(BCVA)测量,包括动态荧光素和ICG血管造影在内的完整眼睛检查以及光学相干断层扫描(OCT)。结果:共纳入18例RAP患者的21眼。平均年龄为77岁(65-86岁)。基线时的平均视力为0.63 +/- 0.25 logMAR。治疗后,BCVA每次访视之间无统计学差异(P = 0.10,ANOVA)。在9个月时,三只眼的BCVA改善了三行或更多(14%),十二只眼保持稳定(57%),六只眼则恶化了(29%)。在基线和所有后续随访之间,中央凹厚度明显降低(P <0.01,ANOVA)。在研究期间总共进行了36次玻璃体内注射,平均每只眼睛1.7次注射(每只眼睛1-3次注射)。没有眼或全身不良事件的报道。结论:玻璃体内贝伐单抗联合PDT治疗RAP可能产生协同作用。这些发现还表明组合疗法对玻璃体内再注射的速率可能具有益处。

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