Mori Ryusaburo, Tanaka Koji, Yuzawa Mitsuko
Division of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, Tokyo, Japan.
Medicine (Baltimore). 2018 Jun;97(25):e11188. doi: 10.1097/MD.0000000000011188.
This study aimed to explore predictors of long-term stabilization of polypoidal choroidal vasculopathy (PCV) lesions and vision in response to injection of intravitreal ranibizumab (IVR). The treated eyes had a baseline best corrected visual acuity (BCVA) of at least 0.6 (logarithm of the minimal angle of resolution (logMAR) 0.22).We treated 45 eyes showing BCVA between 0.6 (logMAR 0.22) and 1.0 (logMAR 0), with IVR for 3 consecutive months. All eyes were confirmed to have subfoveal PCV prior to starting this treatment regimen. Additional IVR was administered at the subsequent monthly visits, if necessitated by evidence of persistent PCV, for up to 23 months after the first ranibizumab injection. The subjects were then carefully followed-up for 24 months, allowing detailed retrospective evaluation of changes in mean BCVA, central retinal thickness (CRT), serous retinal detachment (SRD), hemorrhage, and polypoidal lesion numbers. The relationships between retreatment and each of the baseline characteristics and SRD development during follow-up were analyzed.The mean logMAR BCVAs were 0.111 ± 0.076, 0.068 ± 0.206 (P = .0033) and 0.115 ± 0.265 (P = .27) at baseline and at 12 and 24 months, respectively. At 24 months, 87% of eyes had BCVA of 20/40 or better. Not requiring retreatment between 12 and 23 months was found to be significantly associated with the absence of retinal pigment epithelial detachment (RPED) at baseline (odds ratio: 0.262 (95% confidence interval (CI): 0.073-0.946). The rates of retreatment from 12 to 23 months were significantly higher in eyes with SRD at 6 and 12 months than in those without SRD (P = .004 and P < .001).In conclusion, during 24 months of antivascular endothelial growth factor (VEGF) therapy using ranibizumab for PCV, BCVA was maintained in those with good visual acuity at baseline. Comprehensive analyses revealed RPED at baseline and SRD development during follow-up to correlate significantly with the need for retreatment between 12 and 23 months. Our observations might facilitate tailoring treatments to individual PCV patients.
本研究旨在探讨息肉状脉络膜血管病变(PCV)病变长期稳定以及玻璃体内注射雷珠单抗(IVR)后视力变化的预测因素。接受治疗的眼睛基线最佳矫正视力(BCVA)至少为0.6(最小分辨角对数(logMAR)0.22)。我们对45只BCVA在0.6(logMAR 0.22)至1.0(logMAR 0)之间的眼睛连续3个月进行IVR治疗。在开始该治疗方案之前,所有眼睛均确诊为黄斑下PCV。如果有持续PCV的证据,在首次注射雷珠单抗后的后续每月随访中进行额外的IVR注射,最长可达23个月。然后对受试者进行24个月的仔细随访,以便详细回顾性评估平均BCVA、中心视网膜厚度(CRT)、浆液性视网膜脱离(SRD)、出血和息肉状病变数量的变化。分析了再次治疗与每个基线特征以及随访期间SRD发生之间的关系。基线时、12个月和24个月时的平均logMAR BCVA分别为0.111±0.076、0.068±0.206(P = 0.0033)和0.115±0.265(P = 0.27)。在24个月时,87%的眼睛BCVA达到20/40或更好。发现12至23个月期间无需再次治疗与基线时无视网膜色素上皮脱离(RPED)显著相关(比值比:0.262(95%置信区间(CI):0.073 - 0.946)。6个月和12个月时有SRD的眼睛在12至23个月期间的再次治疗率显著高于无SRD的眼睛(P = 0.004和P < 0.001)。总之,在使用雷珠单抗对PCV进行24个月的抗血管内皮生长因子(VEGF)治疗期间,基线视力良好的患者BCVA得以维持。综合分析显示,基线时的RPED和随访期间SRD的发生与12至23个月期间再次治疗的需求显著相关。我们的观察结果可能有助于为PCV个体患者量身定制治疗方案。