Safety of ranibizumab in routine clinical practice: 1-year retrospective pooled analysis of four European neovascular AMD registries within the LUMINOUS programme

被引:82
作者
Holz, Frank G. [1 ]
Bandello, Francesco [2 ]
Gillies, Mark [3 ]
Mitchell, Paul [4 ]
Osborne, Aaron [5 ]
Sheidow, Tom [6 ]
Souied, Eric [7 ]
Figueroa, Marta S. [8 ]
机构
[1] Univ Bonn, Dept Ophthalmol, D-53127 Bonn, Germany
[2] Univ Vita Salute Sci Inst, Dept Ophthalmol, Milan, Italy
[3] Univ Sydney, Sydney Eye Hosp, Sydney, NSW 2006, Australia
[4] Univ Sydney, Dept Ophthalmol, Sydney, NSW 2006, Australia
[5] Novartis, Dept Ophthalmol, Basel, Switzerland
[6] Ivey Eye Inst, Dept Ophthalmol, Toronto, ON, Canada
[7] Hop Intercommunal Creteil, Serv Ophthalmol, Creteil, France
[8] Ramon & Cajal Univ Hosp, Serv Oftalmol, Madrid, Spain
关键词
Degeneration; Macula; Treatment Medical; OCCLUSION 12-MONTH OUTCOMES; MACULAR DEGENERATION; SUSTAINED BENEFITS; PHARMACOKINETICS; VERTEPORFIN; BEVACIZUMAB;
D O I
10.1136/bjophthalmol-2013-303232
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose Evaluation of 1-year safety profile of intravitreal ranibizumab 0.5mg in neovascular age-related macular degeneration (NV-AMD) within routine clinical practice. Methods The LUMINOUS programme comprises a prospective observational study assessing ranibizumab real-world' safety and clinical effectiveness across licensed indications worldwide and an annual retrospective pooled safety analysis from completed NV-AMD ranibizumab registries. 1-year data from four European registries are available. This retrospective pooled safety analysis assessed 1-year incidence rates for safety events of particular interest (key ocular or systemic events possibly related to the injection procedure or vascular endothelial growth factor inhibition) together with treatment exposure. Patients were treated according to local protocols within the ranibizumab licence. Results Data of 4444 patients from registries in Germany (n=3470), the Netherlands (n=243), Belgium (n=260) and Sweden (n=471) were retrospectively pooled. Between 70.4% and 84.4% of enrolled patients completed 1year of follow-up. Most frequent overall ocular events of particular interest were retinal pigment epithelial tears (27 patients; <1%) and intraocular pressure-related events (12 patients; <0.3%). Most frequent non-ocular event of particular interest was stroke (19 patients; 0.4%); annual incidence of stroke was low across all registries (0.0-0.5%). Conclusions Ranibizumab demonstrated favourable 1-year safety profile for NV-AMD in this routine clinical practice sample, consistent with previous reported trial data. Additional data from a larger patient population are needed to better describe the long-term safety profile of ranibizumab in routine clinical practice and further evaluate risk for infrequent but serious events in real-life' settings. The 5-year LUMINOUS prospective observational study will address this need.
引用
收藏
页码:1161 / 1167
页数:7
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