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首页> 外文期刊>Retina >Everest study: Efficacy and safety of verteporfin photodynamic therapy in combination with ranibizumab or alone versus ranibizumab monotherapy in patients with symptomatic macular polypoidal choroidal vasculopathy
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Everest study: Efficacy and safety of verteporfin photodynamic therapy in combination with ranibizumab or alone versus ranibizumab monotherapy in patients with symptomatic macular polypoidal choroidal vasculopathy

机译:珠穆朗玛峰研究:Verteporfin光动力疗法联合兰尼单抗或单药与兰尼单抗单药治疗有症状的黄斑息肉样脉络膜脉络膜血管病的疗效和安全性

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摘要

Purpose: To assess the effects of verteporfin photodynamic therapy (PDT) combined with ranibizumab or alone versus ranibizumab monotherapy in patients with symptomatic macular polypoidal choroidal vasculopathy. Methods: In this multicenter, double-masked, primarily indocyanine green angiography-guided trial, 61 Asian patients were randomized to verteporfin PDT (standard fluence), ranibizumab 0.5 mg, or the combination. Patients were administered with verteporfin PDT/placebo and initiated with three consecutive monthly ranibizumab/sham injections starting Day 1, and re-treated (Months 3-5) as per predefined criteria. The primary endpoint was the proportion of patients with indocyanine green angiography-assessed complete regression of polyps at Month 6. Secondary endpoints included mean change in best-corrected visual acuity at Month 6 and safety. Results: At Month 6, verteporfin combined with ranibizumab or alone was superior to ranibizumab monotherapy in achieving complete polyp regression (77.8% and 71.4% vs. 28.6%; P < 0.01); mean change ± standard deviation in best-corrected visual acuity (letters) was 10.9 ± 10.9 (verteporfin PDT + ranibizumab), 7.5 ± 10.6 (verteporfin PDT), and 9.2 ± 12.4 (ranibizumab). There were no new safety findings with either drug used alone or in combination. Conclusion: Verteporfin PDT combined with ranibizumab 0.5 mg or alone was superior to ranibizumab monotherapy in achieving complete regression of polyps in this 6-month study in patients with symptomatic macular polypoidal choroidal vasculopathy. All treatments were well tolerated over 6 months.
机译:目的:评估Verteporfin光动力疗法(PDT)联合兰尼单抗或单独与兰尼单抗单药治疗对有症状的黄斑息肉样脉络膜脉络膜血管病的疗效。方法:在这项多中心,双掩蔽,主要是吲哚菁绿血管造影术指导的试验中,将61名亚洲患者随机分配为Verteporfin PDT(标准通量),兰尼单抗0.5 mg或联合使用。从第1天开始,患者接受Verteporfin PDT /安慰剂的治疗,并开始连续3个月每月接受兰尼单抗/假药注射,并按照预定标准重新治疗(3-5月)。主要终点是在第6个月用吲哚菁绿血管造影术评估的息肉完全消退的患者比例。次要终点包括第6个月最佳矫正视力的平均变化和安全性。结果:在第6个月,Verteporfin联合兰尼单抗或单独使用优于兰尼单抗单药治疗,可实现息肉完全消退(分别为77.8%和71.4%对28.6%; P <0.01);最佳矫正视力(字母)的平均变化±标准偏差(分别为10.9±10.9(verteporfin PDT +雷尼单抗),7.5±10.6(verteporfin PDT)和9.2±12.4(ranibizumab)。单独或联合使用药物均未发现新的安全性发现。结论:在这个为期6个月的有症状黄斑息肉样脉络膜脉管炎患者中,Verteporfin PDT联合雷珠单抗0.5 mg或单独使用比雷珠单抗单药治疗可以使息肉完全消退。所有治疗均在6个月内耐受良好。

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