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首页> 外文期刊>Retina >Three-year follow-up of a pilot study of ranibizumab combined with proton beam irradiation as treatment for exudative age-related macular degeneration
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Three-year follow-up of a pilot study of ranibizumab combined with proton beam irradiation as treatment for exudative age-related macular degeneration

机译:雷珠单抗联合质子束辐照治疗渗出性年龄相关性黄斑变性的试验研究的三年随访

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摘要

BACKGROUND: To investigate the safety and tolerability of ranibizumab combined with proton beam irradiation in treating exudative age-related macular degeneration. METHODS: Six eyes (6 subjects) with exudative age-related macular degeneration (4 newly diagnosed; 2 previous treated with ranibizumab) were treated with 4 monthly ranibizumab and 24 GyE proton beam irradiation (2 fractions, 24 hours apart) and seen monthly thereafter and retreated with ranibizumab for decrease in best-corrected visual acuity of ≥2 lines, new macular hemorrhage or fluid noted on optical coherence tomography. RESULTS: Follow-up ranged from 12 months to 36 months (mean, 28 months). Baseline best-corrected visual acuity ranged from 20/40 to 20/250. Final best-corrected visual acuity ranged from 20/25 to 20/400. No radiation retinopathy was noted in any eye. Calculated radiation distribution dose curves indicate that ≤10% of retina received ≥90% of radiation dose in all eyes. Two subjects lost ≥3 lines of best-corrected visual acuity during follow-up, 1 subject in both eyes from enlarging geographic atrophy and the other from worsening fibrovascular pigment epithelial detachment, which was refractory to multiple ranibizumab treatments before enrollment. Among 4 eyes with newly diagnosed exudative age-related macular degeneration, 3 had no fluid on optical coherence tomography at month 12 without further treatment. CONCLUSION: No safety concerns were noted after 3 years in eyes with exudative age-related macular degeneration treated with ranibizumab combined with proton beam irradiation in this small pilot study. A larger randomized prospective study is under way to further evaluate this combination therapy.
机译:背景:探讨兰尼单抗联合质子束照射治疗渗出性年龄相关性黄斑变性的安全性和耐受性。方法:6眼(6名受试者)发生渗出性年龄相关性黄斑变性(4例新诊断; 2例先前接受兰尼单抗治疗),每月接受4枚兰尼单抗和24次GyE质子束辐照(相隔24小时),每次2次并用兰尼单抗治疗,以减少≥2线的最佳矫正视力,新的黄斑出血或光学相干断层扫描显示的积液。结果:随访时间为12个月至36个月(平均28个月)。基线最佳矫正视力范围为20/40至20/250。最终的最佳矫正视力范围为20/25至20/400。任何一只眼睛都没有发现放射性视网膜病变。计算得出的辐射分布剂量曲线表明,在所有眼睛中,≤10%的视网膜接受了≥90%的辐射剂量。两名受试者在随访期间失去了≥3行最佳矫正视力,两只眼睛的一名受试者因地理萎缩而增加,另一名受试者的纤维血管色素上皮脱离恶化,这在入组前因多次兰尼单抗治疗难以治愈。在新诊断为渗出性年龄相关性黄斑变性的4眼中,有3眼在未经进一步治疗的情况下在第12个月时光学相干断层扫描没有积液。结论:在这项小规模的先导研究中,兰尼单抗联合质子束照射治疗3年后与年龄相关的渗出性黄斑变性渗出的眼睛没有安全性问题。正在进行一项更大的随机前瞻性研究,以进一步评估这种联合治疗。

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