首页> 外文期刊>Assay and drug development technologies >Erratum: A phenotypic screening approach to identify anticancer compounds derived from Marine Fungi (Assay and Drug Development Technologies (2014) 12: 3 (162-175))
【24h】

Erratum: A phenotypic screening approach to identify anticancer compounds derived from Marine Fungi (Assay and Drug Development Technologies (2014) 12: 3 (162-175))

机译:勘误表:一种鉴定源自海洋真菌的抗癌化合物的表型筛选方法(测定和药物开发技术(2014)12:3(162-175))

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: To study the visual outcomes and change in central macular thickness (CMT) in patients with neovascular age-related macular degeneration (AMD) who were previously treated with ranibizumab (Lucentis) and/or bevacizumab (Avastin) and were subsequently switched to aflibercept (VEGF Trap-Eye; Eylea). Methods: Retrospective study of patients who received intravitreal aflibercept from December 2011 to December 2012 and had previous anti-vascular endothelial growth factor treatment for AMD. The main outcome measures were best-corrected visual acuity (BCVA) and CMT as measured by optical coherence tomography. Results: The study population included 30 patients aged 80.4±1.45 (mean±SEM) who received 6.27±0.37 (range 4-11) aflibercept injections. Eighteen patients had previously received only bevacizumab (12.4±2.18 injections), 2 had received only ranibizumab (19±6 injections), and 10 had received both ranibizumab and bevacizumab (mean 19.3 injections). BCVA logMAR at the initial visit (aflibercept initiation) was 0.506±0.054 (mean VA 20/64), and then, follow ups at 1-month 0.504±0.055 (20/64) P=0.903, 3-months 0.458±0.061 (20/57) P=0.112, 6-months 0.413±0.071 (20/52) P=0.036, and 12-months 0.521±0.076 (20/66) P=0.836. CMT at the initial visit was 261±10.9, and then, at 1-month 238±12.4 P=0.021, 3-months 245±10.6 P=0.102, 6-months 245±10.4 P=0.099, and 12-months 237±10.2 P=0.012. Results were similar in a subset of patients (n=15) with central macular edema or submacular fluid at aflibercept initiation. While on aflibercept, 2 patients developed intraocular pressure increases that required treatment. Conclusions: These findings demonstrate a significant decrease in CMT but no statistically significant improvement in BCVA through the 12-month follow up in patients previously treated who were switched to aflibercept for AMD. Patients may develop ocular hypertension after multiple aflibercept injections.
机译:目的:研究先前接受兰尼单抗(Lucentis)和/或贝伐单抗(Avastin)治疗并随后改用阿柏西普的新生血管性年龄相关性黄斑变性(AMD)患者的视觉效果和中央黄斑中心厚度(CMT)的变化(VEGF Trap-Eye; Eylea)。方法:回顾性研究2011年12月至2012年12月接受玻璃体内阿柏西普治疗且先前曾接受过抗血管内皮生长因子治疗的AMD患者。主要结局指标是通过光学相干断层扫描测量的最佳矫正视力(BCVA)和CMT。结果:研究人群包括30位80.4±1.45(平均值±SEM)的患者,他们接受了6.27±0.37(范围4-11)的阿柏西普注射。以前仅接受贝伐单抗(12.4±2.18注射)的患者有18名,仅接受了兰尼单抗的治疗(19±6次注射),有10位同时接受了兰尼单抗和贝伐单抗的患者(平均19.3注射)。初次就诊(aflibercept起始)时的BCVA logMAR为0.506±0.054(平均VA 20/64),然后在1个月时随访0.504±0.055(20/64)P = 0.903,3个月时为0.458±0.061( 20/57)P = 0.112,6个月0.413±0.071(20/52)P = 0.036,12个月0.521±0.076(20/66)P = 0.836。初诊时的CMT为261±10.9,然后在1个月238±12.4 P = 0.021、3个月245±10.6 P = 0.102、6个月245±10.4 P = 0.099和12个月237± 10.2 P = 0.012。在aflibercept起始时出现中央性黄斑水肿或黄斑下积液的患者子集中(n = 15),结果相似。在使用abribercept时,有2名患者的眼压升高,需要治疗。结论:这些发现表明,在先前接受过aflibercept接受AMD治疗的患者的12个月随访中,CMT显着降低,但BCVA没有统计学上的显着改善。多次注射阿柏西普后,患者可能出现高眼压。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号