Dipartimento di Scienze per la Salute, Università degli Studi del Molise, Campobasso, Italy.
Br J Ophthalmol. 2010 Feb;94(2):180-4. doi: 10.1136/bjo.2009.159343. Epub 2009 Dec 3.
To report the efficacy and safety of intravitreal bevacizumab (IVB) alone versus IVB plus low-fluence photodynamic therapy (PDT) in age-related macular degeneration (AMD) patients and to verify the occurrence of a synergistic effect of the combined approach on visual acuity, size and morphology of lesion, as well as on the treatment rate.
Prospective comparative interventional study on 85 patients with treatment-naive classic, or predominantly classic, subfoveal choroidal neovascularisation secondary to AMD. Patients were randomly assigned to group 1 (IVB injections) and group 2 (IVB plus low fluence PDT). In group 2, the PDT with verteporfin was delivered with a low fluence rate (300 mW/cm2 for 83 s, 25 J/cm2). The follow-up was scheduled at 1, 3, 6, 9 and 12 months.
The eye without recurrence received a mean of 2.8 (group 1) versus 1.4 (group 2) IVB injections, whereas the eyes with recurrence received a mean of 3.2 (group 1) versus 2.2 (group 2) IVB injections. The difference in reinjection rate between the two groups was statistically significant (p=0.03, ANOVA test). Visual acuity improvement was not statistically significant between the two groups (p=0.31).
The combination of IVB with low fluence PDT for the treatment of classic or predominantly classic neovascular AMD works in a synergistic fashion with a significant reduction in IVB reinjections rate.
报告玻璃体内注射贝伐单抗(IVB)单独治疗与 IVB 联合低强度光动力疗法(PDT)治疗年龄相关性黄斑变性(AMD)患者的疗效和安全性,并验证联合治疗在视力、病变大小和形态以及治疗率方面是否存在协同作用。
对 85 例未经治疗的经典或主要经典型黄斑下脉络膜新生血管化 AMD 患者进行前瞻性比较干预研究。患者随机分为 1 组(IVB 注射)和 2 组(IVB 联合低强度 PDT)。2 组患者均行维替泊芬低强度 PDT,光强度为 300 mW/cm2 ,时间为 83 秒,能量密度为 25 J/cm2。随访时间为 1、3、6、9 和 12 个月。
无复发眼平均接受 2.8 次(组 1)与 1.4 次(组 2)IVB 注射,而复发眼平均接受 3.2 次(组 1)与 2.2 次(组 2)IVB 注射。两组间再注射率差异有统计学意义(p=0.03,方差分析)。两组间视力提高无统计学差异(p=0.31)。
IVB 联合低强度 PDT 治疗经典或主要经典型新生血管性 AMD 具有协同作用,可显著降低 IVB 再注射率。