Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing, Dongcheng District, Beijing, 100730, China.
Key Laboratory of Ocular Fundus Diseases, Chinese Academy of Medical Sciences, Beijing, China.
BMC Ophthalmol. 2019 Nov 21;19(1):237. doi: 10.1186/s12886-019-1245-4.
To evaluate 5-year outcomes of anti-vascular endothelial growth factor (VEGF) monotherapy and combination therapy of anti-VEGF agents and photodynamic therapy (PDT) for polypoidal choroidal vasculopathy (PCV) in a real-world Chinese population.
Retrospective study. Fifty-three eyes of 46 patients with subtype 1 and 2 PCV followed up for at least 60 months were grouped into three regimens: anti-VEGF monotherapy, PDT combining with anti-VEGF therapy initially, and PDT combining with deferred anti-VEGF therapy. Main outcome measure was best-corrected visual acuity (BCVA) using logarithm of minimal angle of resolution (logMAR).
The mean BCVA of eyes with subtype 1 PCV (n = 28) deteriorated from 0.69 logMAR at baseline to 1.25 logMAR at months 60 (P = 0.001), while the mean BCVA of eyes with subtype 2 PCV (n = 25) sustained stable from 0.62 logMAR at baseline to 0.57 at months 60 (P = 0.654). No significant differences of visual outcomes were found between the 3 treatment regimens for subtype 1 PCV. Anti-VEGF monotherapy and initial combination treatment had better visual outcomes in eyes with subtype 2 PCV than deferred combination group during part of follow-up significantly. Initial combination group needed a less number of PDT than deferred combination group (P < 0.001).
Compared with subtype 1 PCV, subtype 2 PCV has a more favorable visual outcome in real world. All the regimens presented unfavorable visual outcomes for subtype 1 PCV. Anti-VEGF monotherapy and initial combination therapy should be superior to deferred combination therapy in the long-term management of subtype 2 PCV. Prospective randomized studies of larger size are needed to determine the long-term efficacy and safety of various treatment for PCV in real world.
评估在真实中国人群中,抗血管内皮生长因子(VEGF)单药治疗以及抗 VEGF 药物联合光动力疗法(PDT)治疗息肉样脉络膜血管病变(PCV)的 5 年疗效。
回顾性研究。46 例(53 只眼)1 型和 2 型 PCV 患者,至少随访 60 个月,分为三组:抗 VEGF 单药治疗组、初始 PDT 联合抗 VEGF 治疗组和 PDT 联合延迟抗 VEGF 治疗组。主要观察指标为最佳矫正视力(BCVA),采用最小分辨角对数(logMAR)表示。
1 型 PCV(n=28)眼的平均 BCVA 从基线时的 0.69 logMAR 恶化至 60 个月时的 1.25 logMAR(P=0.001),而 2 型 PCV(n=25)眼的平均 BCVA 从基线时的 0.62 logMAR 稳定至 60 个月时的 0.57(P=0.654)。三种治疗方案对 1 型 PCV 眼的视力结果均无显著差异。在部分随访期间,与延迟联合组相比,抗 VEGF 单药治疗和初始联合治疗对 2 型 PCV 眼的视力结果更好。与延迟联合组相比,初始联合组行 PDT 的次数更少(P<0.001)。
与 1 型 PCV 相比,真实世界中 2 型 PCV 的视力预后更好。所有方案对 1 型 PCV 均显示出不利的视力结果。抗 VEGF 单药治疗和初始联合治疗可能优于延迟联合治疗,用于 2 型 PCV 的长期管理。需要更大规模的前瞻性随机研究来确定各种治疗方法在真实世界中治疗 PCV 的长期疗效和安全性。