Comparison of loading doses of ziv-aflibercept and aflibercept in neovascular age-related macular degeneration
| dc.contributor.author | Ayachit, Apoorva G. | |
| dc.contributor.author | Singh, Sumit Randhir | |
| dc.contributor.author | Subramanyam, Anand | |
| dc.contributor.author | Tiwari, Sarvesh | |
| dc.contributor.author | Heranjal, Abhishek | |
| dc.contributor.author | Chattannavar, Goura | |
| dc.contributor.author | Pandey, Priti | |
| dc.contributor.author | Salti, Haytham I.S. | |
| dc.contributor.author | Mansour, Mohamad A. | |
| dc.contributor.author | Mansour, Ahmad Mohammed Farid Mahmoud | |
| dc.contributor.author | Chhablani, Jay Kumar | |
| dc.contributor.department | Ophthalmology | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T12:08:43Z | |
| dc.date.available | 2025-01-24T12:08:43Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | Purpose:The aim of this study was to compare outcomes of 3 loading doses of ziv-aflibercept and aflibercept in treatment-naïve neovascular age-related macular degeneration (nAMD).Design:Retrospective, nonrandomized, comparative study.Methods:This was a retrospective chart review which included cases with treatment-naïve nAMD. The patients were divided into 2 groups (group 1, ziv-aflibercept; group 2, aflibercept). Groups 1 and 2 received 1.25 mg/0.05 mL of intravitreal ziv-aflibercept and 2 mg/0.05 mL aflibercept, respectively every month for 3 months. Best-corrected visual acuity (BCVA) in Snellen and logarithm of minimum angle of resolution (logMAR), central subfoveal thickness (CSFT), subretinal hyperreflective material height, neurosensory detachment height, and pigment epithelial detachment height were recorded at baseline and 3 monthly follow-up.Results:Twenty-three eyes of 23 patients were included (males 14, females 9). Twelve and 11 eyes were included in group 1 and group 2, respectively. Group 1 showed statistically significant improvement in BCVA (P < 0.001) and CSFT (P=0.007) through 3 months compared with baseline. There was significant change in BCVA from baseline at 1st month (P = 0.007), 2nd month (P = 0.002) and 3rd month (P = 0.008). In group 2, there was no significant improvement in BCVA, CSFT, subretinal hyperreflective material height, neurosensory detachment, and pigment epithelial detachment height from baseline through 3 months.Conclusions:After 3 loading doses, ziv-aflibercept showed efficacy in terms of improved BCVA and reduction of CSFT from baseline whereas aflibercept did not show such improvement. Considering the cost- effectiveness and the proven safety of ziv-aflibercept, it is a viable option for the crucial, initial 3 doses in the treatment of nAMD. © 2020 Asia-Pacific Academy of Ophthalmology. All rights reserved. | |
| dc.identifier.doi | https://doi.org/10.1097/APO.0000000000000277 | |
| dc.identifier.eid | 2-s2.0-85084175109 | |
| dc.identifier.pmid | 32175924 | |
| dc.identifier.uri | http://hdl.handle.net/10938/31894 | |
| dc.language.iso | en | |
| dc.publisher | Lippincott Williams and Wilkins | |
| dc.relation.ispartof | Asia-Pacific Journal of Ophthalmology | |
| dc.source | Scopus | |
| dc.subject | Aflibercept | |
| dc.subject | Neovascular age related macular degeneration (n-amd) | |
| dc.subject | Ziv-aflibercept | |
| dc.subject | Aged | |
| dc.subject | Aged, 80 and over | |
| dc.subject | Angiogenesis inhibitors | |
| dc.subject | Choroidal neovascularization | |
| dc.subject | Female | |
| dc.subject | Fluorescein angiography | |
| dc.subject | Follow-up studies | |
| dc.subject | Humans | |
| dc.subject | Intravitreal injections | |
| dc.subject | Male | |
| dc.subject | Receptors, vascular endothelial growth factor | |
| dc.subject | Recombinant fusion proteins | |
| dc.subject | Retrospective studies | |
| dc.subject | Tomography, optical coherence | |
| dc.subject | Treatment outcome | |
| dc.subject | Vascular endothelial growth factor a | |
| dc.subject | Visual acuity | |
| dc.subject | Wet macular degeneration | |
| dc.subject | Angiogenesis inhibitor | |
| dc.subject | Fusion protein | |
| dc.subject | Vasculotropin a | |
| dc.subject | Vasculotropin receptor | |
| dc.subject | Vegfa protein, human | |
| dc.subject | Comparative study | |
| dc.subject | Diagnostic imaging | |
| dc.subject | Fluorescence angiography | |
| dc.subject | Follow up | |
| dc.subject | Human | |
| dc.subject | Intravitreal drug administration | |
| dc.subject | Optical coherence tomography | |
| dc.subject | Pathophysiology | |
| dc.subject | Physiology | |
| dc.subject | Retrospective study | |
| dc.subject | Subretinal neovascularization | |
| dc.subject | Very elderly | |
| dc.title | Comparison of loading doses of ziv-aflibercept and aflibercept in neovascular age-related macular degeneration | |
| dc.type | Article |
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