Ziemssen Focke, Lüke Matthias, Messias Andre, Beutel Julia, Tatar Olcay, Zrenner Eberhart, Bartz-Schmidt Karl U
Department for Ophthalmology, Eberhard-Karls University Tuebingen, Tuebingen, Germany.
Int Ophthalmol. 2008 Apr;28(2):101-9. doi: 10.1007/s10792-007-9122-1. Epub 2007 Jul 20.
Bevacizumab (Avastin) has been used as off-label treatment for the specific inhibition of the vascular endothelial growth factor (VEGF). Although only intravenous administration of the drug is approved in combination therapy of colorectal carcinoma, promising short-term results have been reported about its intravitreal administration. However, VEGF is also known to exhibit neurotrophic capabilities. Therefore, blockage of all VEGF isoforms by bevacizumab could induce toxic effects. Missing randomized controlled studies and unclear long-term risks require further evaluation.
Intensified monitoring of bevacizumab treatment was performed in consecutive patients. In ten patients, the functional field score was calculated after obtaining Goldmann visual fields at baseline and 1 year after injection. The other subgroup was examined by means of EOG, ERG and colour testing at baseline and 4 months following treatment. Naka-Rushton plots were calculated to enable statements about retinal function. Lanthony desaturated D15 test was used for repeated colour testing.
Baseline parameters already disclosed predominant cone dysfunction. Drug-related effects caused a significant improvement of visual acuity. There was no sign of clinically relevant retinal toxicity following the bevacizumab injection. No progression of visual field defects was seen within the follow-up of 1 year. Performance in EOG testing was affected by restricted fixation stability, but no parameter indicated deterioration within the 4-month-period.
Short-term results underline that intraocular bevacizumab injection promises to be not only a cost-effective, but safe treatment option. Assessed functional parameters as error scores (e.g., Lanthony) corresponded to the impaired retinal function which was presumed to be disease-related. Further long-term results have to confirm the good tolerability in repeated treatment.
贝伐单抗(阿瓦斯汀)已被用作血管内皮生长因子(VEGF)特异性抑制的非标签治疗药物。尽管该药物仅在结直肠癌联合治疗中的静脉给药获得批准,但有关其玻璃体内给药的短期效果报告显示前景良好。然而,VEGF也具有神经营养能力。因此,贝伐单抗阻断所有VEGF异构体可能会诱发毒性作用。缺乏随机对照研究以及长期风险不明确,需要进一步评估。
对连续患者进行贝伐单抗治疗的强化监测。在10名患者中,在基线和注射后1年获得戈德曼视野后计算功能视野评分。另一亚组在基线和治疗后4个月通过EOG、ERG和颜色测试进行检查。计算中纳-拉什顿图以评估视网膜功能。使用兰托尼去饱和D15测试进行重复颜色测试。
基线参数已显示主要为视锥细胞功能障碍。药物相关效应使视力显著改善。贝伐单抗注射后未出现临床相关视网膜毒性迹象。在1年的随访期内未观察到视野缺损进展。EOG测试的表现受注视稳定性受限影响,但在4个月期间内没有参数表明恶化。
短期结果表明,玻璃体内注射贝伐单抗不仅有望成为一种具有成本效益的治疗选择,而且是安全的。评估的功能参数作为误差评分(例如兰托尼)与推测与疾病相关的视网膜功能受损相对应。进一步的长期结果必须证实重复治疗的良好耐受性。