Yoneda Ai, Wakiyama Harumi, Kurihara Junko, Kitaoka Takashi
Department of Ophthalmology, The Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki, Japan.
Department of Ophthalmology and Visual Sciences, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Eur J Ophthalmol. 2020 Nov;30(6):1473-1479. doi: 10.1177/1120672119871886. Epub 2019 Sep 2.
To compare the 2-year outcomes of combination therapy using intravitreal ranibizumab and photodynamic therapy with those of fixed-dosing intravitreal aflibercept monotherapy as initial treatment for treatment-naïve polypoidal choroidal vasculopathy.
We retrospectively reviewed 63 eyes of 61 patients with treatment-naïve polypoidal choroidal vasculopathy who had undergone at least 24 months of follow-up. In total, 43 eyes underwent intravitreal ranibizumab-photodynamic therapy combination therapy and 20 eyes underwent fixed-dosing intravitreal aflibercept monotherapy. Visual outcomes and the number of treatments were compared between the two groups.
The mean logarithm of minimal angle of resolution best-corrected visual acuity significantly improved from 0.48 ± 0.41 at baseline to 0.30 ± 0.47 at 24 months in the intravitreal ranibizumab-photodynamic therapy group ( = .0002) and from 0.30 ± 0.18 at baseline to 0.16 ± 0.18 at 24 months in the intravitreal aflibercept group ( = .004), with no significant intergroup differences. The mean number of intravitreal ranibizumab or intravitreal aflibercept injections over 24 months was 5.7 ± 4.5 in the intravitreal ranibizumab-photodynamic therapy group and 12.2 ± 3.8 in the intravitreal aflibercept group ( < .0001).
The intravitreal ranibizumab-photodynamic therapy combination therapy was noninferior to fixed-dosing intravitreal aflibercept monotherapy in improving visual acuity and required fewer injections.
比较玻璃体内注射雷珠单抗联合光动力疗法与固定剂量玻璃体内注射阿柏西普单药疗法作为初治息肉状脉络膜血管病变初始治疗的2年疗效。
我们回顾性分析了61例初治息肉状脉络膜血管病变患者的63只眼,这些患者均接受了至少24个月的随访。其中,43只眼接受了玻璃体内注射雷珠单抗联合光动力疗法,20只眼接受了固定剂量玻璃体内注射阿柏西普单药疗法。比较两组的视力结果和治疗次数。
玻璃体内注射雷珠单抗联合光动力疗法组的最小分辨角对数视力从基线时的0.48±0.41显著提高至24个月时的0.30±0.47(P = 0.0002),玻璃体内注射阿柏西普组从基线时的0.30±0.18提高至24个月时的0.16±0.18(P = 0.004),组间差异无统计学意义。玻璃体内注射雷珠单抗联合光动力疗法组24个月内玻璃体内注射雷珠单抗或阿柏西普的平均次数为5.7±4.5次,玻璃体内注射阿柏西普组为12.2±3.8次(P < 0.0001)。
玻璃体内注射雷珠单抗联合光动力疗法在提高视力方面不劣于固定剂量玻璃体内注射阿柏西普单药疗法,且所需注射次数更少。