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Combined photodynamic therapy with intravitreal bevacizumab injections for polypoidal choroidal vasculopathy: long-term visual outcome.联合光动力疗法与玻璃体内注射贝伐单抗治疗息肉样脉络膜血管病变:长期视力结果。
Am J Ophthalmol. 2014 Mar;157(3):598-606.e1. doi: 10.1016/j.ajo.2013.11.015. Epub 2013 Nov 22.
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Comparison of the effect of ranibizumab and verteporfin for polypoidal choroidal vasculopathy: 12-month LAPTOP study results.比较雷珠单抗和维替泊芬治疗息肉样脉络膜血管病变的效果:LAPTOP 研究 12 个月结果。
Am J Ophthalmol. 2013 Oct;156(4):644-51. doi: 10.1016/j.ajo.2013.05.024. Epub 2013 Jul 20.
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Factors predictive of outcomes 1 year after 3 monthly ranibizumab injections and as-needed reinjections for polypoidal choroidal vasculopathy in Japanese patients.预测日本患者息肉状脉络膜血管病变接受每 3 个月雷珠单抗注射和按需再注射治疗 1 年后结局的因素。
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Two-year results of combined intravitreal ranibizumab and photodynamic therapy for polypoidal choroidal vasculopathy.联合玻璃体内雷珠单抗和光动力疗法治疗息肉状脉络膜血管病变的两年结果。
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Combined intravitreal ranibizumab and photodynamic therapy for polypoidal choroidal vasculopathy.眼内联合雷珠单抗和光动力疗法治疗息肉状脉络膜血管病变。
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Factors associated with the response of age-related macular degeneration to intravitreal ranibizumab treatment.与年龄相关性黄斑变性对玻璃体内雷珠单抗治疗反应相关的因素。
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One-year results of three monthly ranibizumab injections and as-needed reinjections for polypoidal choroidal vasculopathy in Japanese patients.日本患者息肉状脉络膜血管病变接受每月三次雷珠单抗注射和按需再注射的一年结果。
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Idiopathic polypoidal choroidal vasculopathy (IPCV). 1990.特发性息肉样脉络膜血管病变(IPCV)。1990 年。
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10
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.EVEREST 研究:维替泊芬光动力疗法联合雷珠单抗或单用与雷珠单抗单药治疗有症状的黄斑息肉样脉络膜血管病变患者的疗效和安全性。
Retina. 2012 Sep;32(8):1453-64. doi: 10.1097/IAE.0b013e31824f91e8.

雷珠单抗联合光动力疗法治疗息肉状脉络膜血管病变1年的疗效及影响疗效的预测因素

Outcome of polypoidal choroidal vasculopathy at 1 year by combined therapy of photodynamic therapy with ranibizumab and predictive factors governing the outcome.

作者信息

Ho M, Lo E C F, Young A L, Liu D T L

机构信息

Department of Ophthalmology & Visual Sciences, Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong SAR, Hong Kong.

出版信息

Eye (Lond). 2014 Dec;28(12):1469-76. doi: 10.1038/eye.2014.222. Epub 2014 Sep 26.

DOI:10.1038/eye.2014.222
PMID:25257771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4268462/
Abstract

AIM

To report the visual outcome of polypoidal choroidal vasculopathy receiving combined treatment with photodynamic therapy using Visudyne and intravitreal ranibizumab injections, and to analyze the predictive factors of visual outcome at 1 year post treatment.

METHODS

Seventy-four consecutive patients with newly diagnosed polypoidal choroidal vasculopathy were treated with photodynamic therapy using Visudyne and three loading doses of intravitreal ranibizumab. The final visual outcome and polyp eradication rate at 1 year were reported. A stepwise regression model was used to estimate the baseline clinical factors predictive of better visual outcome and polyp eradication.

RESULTS

Visual acuities at 12-months follow-up improved significantly compared with baseline from 0.828 logMAR to 0.728 logMAR (P=0.026). The mean foveal thickness decreased from 380±175 to 278±117 μm. In all 29.7% of eyes improved at least by 0.3 logMAR, and 55.4% remained stable in visual acuity with less than 0.3 logMAR change. Overall, 85% of eyes achieved at least stable vision, 20.2% (15/74) cases achieved polyp eradication on angiogram, and 60.8% (45/74) achieved polyp size reduction on angiogram at 1 year. Regarding predictive factors, the baseline visual acuity (P=0.003), no foveal involvement by abnormal choroidal vasculature (P<0.0001), absence of hard exudates (0.001) or subretinal fluid (<0.0001) are important clinical factors affecting the final visual outcome.

CONCLUSIONS

Combination therapy with photodynamic therapy using Visudyne and three loading doses of intravitreal ranibizumab injections resulted in 85% success rate on visual stabilization and 81% success rate in polypoidal lesion control.

摘要

目的

报告接受维速达尔光动力疗法联合玻璃体内注射雷珠单抗治疗的息肉样脉络膜血管病变的视力结果,并分析治疗后1年视力结果的预测因素。

方法

74例新诊断的息肉样脉络膜血管病变患者接受了维速达尔光动力疗法及3次负荷剂量的玻璃体内雷珠单抗注射治疗。报告了1年时的最终视力结果及息肉消除率。采用逐步回归模型评估预测视力改善及息肉消除的基线临床因素。

结果

随访12个月时的视力与基线相比显著改善,从0.828 logMAR提高至0.728 logMAR(P = 0.026)。平均黄斑中心凹厚度从380±175μm降至278±117μm。所有患眼中,29.7%至少提高了0.3 logMAR,55.4%的视力保持稳定,变化小于0.3 logMAR。总体而言,85%的患眼至少实现了视力稳定,20.2%(15/74)的病例在血管造影上实现了息肉消除,60.8%(45/74)的病例在血管造影上实现了息肉大小缩小。关于预测因素,基线视力(P = 0.003)、异常脉络膜血管未累及黄斑中心凹(P < 0.0001)、无硬性渗出(0.001)或视网膜下液(< 0.0001)是影响最终视力结果的重要临床因素。

结论

维速达尔光动力疗法联合3次负荷剂量的玻璃体内雷珠单抗注射治疗,视力稳定成功率为85%,息肉样病变控制成功率为81%。