Department of Ophthalmology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
Department of Pediatrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Biomed Res Int. 2020 Apr 23;2020:2428348. doi: 10.1155/2020/2428348. eCollection 2020.
To compare the efficacy between initial 3-monthly intravitreal conbercept monotherapy and combination intravitreal conbercept with photodynamic therapy (PDT) for polypoidal choroidal vasculopathy (PCV).
This is a retrospective, comparative study which involved 65 PCV eyes of 65 patients. According to the therapeutic regimen, the PCV patients were divided into two groups: 32 eyes with naive PCV received a PDT after the first intravitreal injection of conbercept (IVC) followed by pro re nata (prn) retreatment (combination group), and 33 eyes with naïve PCV received 3-monthly IVC monotherapy followed by prn regimen (IVC monotherapy group). All patients completed at least 6 months of monthly follow-up.
At month 6, best-corrected visual acuity (BCVA) improved significantly ( < 0.05) in both groups compared with that at baseline; the mean changes of BCVA between the IVC monotherapy group and combination group have no significant difference (-0.22 ± 0.22 vs. -0.17 ± 0.22 LogMAR, = 0.38). The central retinal thickness (CRT) decreased significantly in the two groups ( < 0.05), with no difference between the two groups ( = 0.24). The complete regression rate of polyps was 58.6% (17 out of 29 eyes) in the IVC monotherapy group and 80.65% (25 out of 31 eyes) in the combination group, respectively ( = 0.09, -squared test). The combination group required significantly fewer injections than the IVC monotherapy group (3.09 ± 0.89 vs. 3.67 ± 0.74, = 0.006).
Conbercept monotherapy significantly improved visual acuity and effectively regressed polyps during 6-month follow-up time in the treatment of PCV.
比较初始 3 个月玻璃体腔内康柏西普单药治疗与联合玻璃体腔内康柏西普联合光动力疗法(PDT)治疗息肉状脉络膜血管病变(PCV)的疗效。
这是一项回顾性比较研究,共纳入 65 例 65 只眼 PCV 患者。根据治疗方案,将 PCV 患者分为两组:32 只眼初次玻璃体腔内注射康柏西普后行 PDT 治疗(联合组),继以按需治疗(prn);33 只眼初次玻璃体腔内注射康柏西普后行 3 个月玻璃体腔内注射康柏西普单药治疗(康柏西普单药组),继以 prn 治疗。所有患者均完成至少 6 个月的每月随访。
治疗 6 个月时,两组最佳矫正视力(BCVA)均较基线显著提高(<0.05);康柏西普单药组与联合组 BCVA 变化的均值差异无统计学意义(-0.22±0.22 与-0.17±0.22 LogMAR,=0.38)。两组中央视网膜厚度(CRT)均显著降低(<0.05),但两组间差异无统计学意义(=0.24)。康柏西普单药组和联合组息肉完全消退率分别为 58.6%(29 眼中 17 只眼)和 80.65%(31 眼中 25 只眼)(=0.09,卡方检验)。联合组所需注射次数明显少于康柏西普单药组(3.09±0.89 与 3.67±0.74,=0.006)。
康柏西普单药治疗在 6 个月的随访时间内显著提高了视力,并有效消退了 PCV 中的息肉。