Laiginhas Rita, Silva Marta Inês, Rosas Vitor, Penas Susana, Fernandes Vitor Adriano, Rocha-Sousa Amândio, Carneiro Ângela, Falcão-Reis Fernando, Falcão Manuel Sousa
Department of Ophthalmology, Centro Hospitalar de São João, Porto, Portugal.
Centro Hospitalar de Entre o Douro e Vouga, Santa Maria da Feira, Portugal.
Graefes Arch Clin Exp Ophthalmol. 2018 Jan;256(1):83-89. doi: 10.1007/s00417-017-3836-1. Epub 2017 Oct 29.
To evaluate functional and anatomical outcomes after aflibercept in patients with diabetic macular edema (DME) with poor response to bevacizumab.
We retrospectively reviewed patients with DME recalcitrant to bevacizumab who were switched to aflibercept between January and December 2015. All patients had a minimal follow-up of three months before the conversion and underwent at least three injections of bevacizumab. Functional outcome consisted in best corrected visual acuity (VA). Anatomical outcomes were demonstrated through central macular thickness (CMT) measured by optical coherence tomography.
Forty-nine eyes of 34 subjects were reviewed. Mean VA improved from 0.55 ± 0.32 logMAR to 0.46 ± 0.33 logMAR (p = 0.038). Mean CMT decreased from 473 ± 146 μm to 349 ± 85 μm (p < 0.001). Twelve eyes (24%) demonstrated absence of macular edema after aflibercept. Previous bevacizumab exposure did not correlate with different outcomes. The variation of VA in response to aflibercept was significantly superior in the group with poorer VA before the switch (mean variation of -0.097 ± 0.21 logMAR) when compared to eyes with VA < 0.4 logMAR (mean variation of +0.019 ± 0.090 logMAR; p = 0.036). The same scenario was verified for anatomical outcomes as eyes with poor vision before the switch (≥0.4 logMAR) achieved superior reduction in CMT in response to aflibercept (mean CMT variation of -157 ± 171 μm versus -49.5 ± 39.9 μm; p < 0.01). Pre-switch CMT was a predictor of CMT reduction after switching (B = -0.945; confidence interval 95% -1.1; -0.76; p < 0.001).
Conversion to aflibercept for persistent DME resulted in functional and anatomical improvements and these outcomes were not influenced by previous bevacizumab exposure. Pre-switch CMT was a predictor of anatomical changes after aflibercept.
评估对贝伐单抗反应不佳的糖尿病性黄斑水肿(DME)患者接受阿柏西普治疗后的功能和解剖学结局。
我们回顾性分析了2015年1月至12月间从贝伐单抗转换为阿柏西普治疗的难治性DME患者。所有患者在转换前至少随访3个月,并接受了至少3次贝伐单抗注射。功能结局以最佳矫正视力(VA)衡量。通过光学相干断层扫描测量中心黄斑厚度(CMT)来评估解剖学结局。
共纳入34例患者的49只眼。平均视力从0.55±0.32 logMAR提高到0.46±0.33 logMAR(p = 0.038)。平均CMT从473±146μm降至349±85μm(p < 0.001)。12只眼(24%)在接受阿柏西普治疗后黄斑水肿消失。既往贝伐单抗治疗史与不同结局无关。与转换前视力<0.4 logMAR的眼相比,转换前视力较差组(平均变化-0.097±0.21 logMAR)对阿柏西普治疗的视力变化明显更优(平均变化+0.019±0.090 logMAR;p = 0.036)。解剖学结局方面也有同样情况,转换前视力较差(≥0.4 logMAR)的眼对阿柏西普治疗的CMT降低更显著(平均CMT变化-157±171μm对-49.5±39.9μm;p < 0.01)。转换前CMT是转换后CMT降低的预测指标(B = -0.945;95%置信区间-1.1;-0.76;p < 0.001)。
将持续性DME转换为阿柏西普治疗可改善功能和解剖学结局,且这些结局不受既往贝伐单抗治疗的影响。转换前CMT是阿柏西普治疗后解剖学变化的预测指标。