Korean J Ophthalmol.  2014 Dec;28(6):466-472. 10.3341/kjo.2014.28.6.466.

Intravitreal Anti-vascular Endothelial Growth Factor for Typical Exudative Age-related Macular Degeneration in Eyes with Good Baseline Visual Acuity

Affiliations
  • 1Department of Ophthalmology, Konyang University College of Medicine, Daejeon, Korea.
  • 2Department of Ophthalmology, Kim's Eye Hospital, Konyang University College of Medicine, Seoul, Korea. kimoph@gmail.com

Abstract

PURPOSE
To investigate 12-month treatment outcomes of anti-vascular endothelial growth factor therapy in eyes with typical exudative age-related macular degeneration with good baseline visual acuity.
METHODS
This retrospective observational case series included 18 eyes (18 patients) with typical exudative age-related macular degeneration with a baseline best-corrected visual acuity of 20 / 25 or better. Patients were treated with anti-vascular endothelial growth factor monotherapy during the 12-month follow-up period. Baseline visual acuity and central foveal thickness were compared to the values at 12 months.
RESULTS
Patients received an average of 4.4 +/- 1.3 intravitreal anti-vascular endothelial growth factor injections. The mean logarithm of minimum angle of resolution visual acuity was 0.08 +/- 0.04, 0.08 +/- 0.07, 0.12 +/- 0.09, and 0.16 +/- 0.11 at baseline, three months, six months, and 12 months, respectively. Visual acuity at 12 months was significantly worse than the baseline value at diagnosis (p = 0.017), and the mean central foveal thickness at the defined time points was 270.2 +/- 55.6, 204.4 +/- 25.4, 230.1 +/- 56.3, and 216.8 +/- 48.7 microm, respectively. The central foveal thickness at 12 months was significantly less than the baseline value at diagnosis (p = 0.042).
CONCLUSIONS
Deterioration in visual acuity was noted in eyes with typical exudative age-related macular degeneration with good baseline visual acuity, suggesting the need for close patient monitoring and prompt treatment even in patients with good baseline visual acuity.

Keyword

Anti-vascular endothelial growth factor; Bevacizumab; Good visual acuity; Macular degeneration; Ranibizumab

MeSH Terms

Aged
Angiogenesis Inhibitors/*therapeutic use
Bevacizumab/therapeutic use
Choroidal Neovascularization/*drug therapy/physiopathology
Female
Fluorescein Angiography
Humans
Intravitreal Injections
Male
Middle Aged
Ranibizumab/therapeutic use
Retrospective Studies
Tomography, Optical Coherence
Vascular Endothelial Growth Factor A/antagonists & inhibitors
Visual Acuity/*physiology
Wet Macular Degeneration/*drug therapy/physiopathology
Angiogenesis Inhibitors
Bevacizumab
Ranibizumab
Vascular Endothelial Growth Factor A

Figure

  • Fig. 1 Changes in mean logarithm of minimum angle of resolution (logMAR) best-corrected visual acuity (BCVA, A) and central foveal thickness (B) in eyes diagnosed with typical exudative age-related macular degeneration with good baseline visual acuity. Statistical analyses were performed using repeated measures analysis of variances with Bonferroni's correction.

  • Fig. 2 Fluorescein angiography (A) and optical coherence tomography (B,C,D) findings in an eye with typical exudative age-related macular degeneration. The best-corrected visual acuity at the time of diagnosis was 20 / 25 (A,B). The eye received six ranibizumab injections during the 12-month follow-up period, but the subretinal lesion enlarged, as seen on optical coherence tomography at six (C) and 12 (D) months. A decrease in visual acuity to 20 / 50 was observed at 12 months.

  • Fig. 3 Fluorescein angiography (A) and optical coherence tomography (B,C,D) findings of an eye diagnosed with typical exudative age-related macular degeneration. The best-corrected visual acuity at the time of diagnosis was 20 / 25 (A,B). After three consecutive ranibizumab injections, exudation recurrence was not noted during the 12-month follow-up period, as verified by optical coherence tomography at six (C) and 12 (D) months. The best-corrected visual acuity at 12 months was maintained at 20 / 25.


Reference

1. Rosenfeld PJ, Brown DM, Heier JS, et al. Ranibizumab for neovascular age-related macular degeneration. N Engl J Med. 2006; 355:1419–1431.
2. Lee SY, Kim JG, Joe SG, et al. The therapeutic effects of bevacizumab in patients with polypoidal choroidal vasculopathy. Korean J Ophthalmol. 2008; 22:92–99.
3. Cho HJ, Baek JS, Lee DW, et al. Short-term effectiveness of intravitreal bevacizumab vs. ranibizumab injections for patients with polypoidal choroidal vasculopathy. Korean J Ophthalmol. 2012; 26:157–162.
4. Mones J, Biarnes M, Trindade F, Casaroli-Marano R. FUSION regimen: ranibizumab in treatment-naïve patients with exudative age-related macular degeneration and relatively good baseline visual acuity. Graefes Arch Clin Exp Ophthalmol. 2012; 250:1737–1744.
5. Takahashi M, Sato T, Kishi S. Intravitreal bevacizumab for age-related macular degeneration with good visual acuity. Jpn J Ophthalmol. 2010; 54:565–570.
6. Axer-Siegel R, Bor E, Bourla DH, et al. Intravitreal bevacizumab treatment for exudative age-related macular degeneration with good visual acuity. Retina. 2012; 32:1811–1820.
7. Mori R, Yuzawa M, Akaza E, Haruyama M. Treatment results at 1 year of ranibizumab therapy for polypoidal choroidal vasculopathy in eyes with good visual acuity. Jpn J Ophthalmol. 2013; 57:365–371.
8. Shona O, Gupta B, Vemala R, Sivaprasad S. Visual acuity outcomes in ranibizumab-treated neovascular age-related macular degeneration; stratified by baseline vision. Clin Experiment Ophthalmol. 2011; 39:5–8.
9. Matsumiya W, Honda S, Kusuhara S, et al. Effectiveness of intravitreal ranibizumab in exudative age-related macular degeneration (AMD): comparison between typical neovascular AMD and polypoidal choroidal vasculopathy over a 1 year follow-up. BMC Ophthalmol. 2013; 13:10.
10. Yamashiro K, Tomita K, Tsujikawa A, et al. Factors associated with the response of age-related macular degeneration to intravitreal ranibizumab treatment. Am J Ophthalmol. 2012; 154:125–136.
11. Fung AE, Lalwani GA, Rosenfeld PJ, et al. An optical coherence tomography-guided, variable dosing regimen with intravitreal ranibizumab (Lucentis) for neovascular age-related macular degeneration. Am J Ophthalmol. 2007; 143:566–583.
12. Liu TY, Shah AR, Del Priore LV. Progression of lesion size in untreated eyes with exudative age-related macular degeneration: a meta-analysis using Lineweaver-Burk plots. JAMA Ophthalmol. 2013; 131:335–340.
13. Arias L, Ruiz-Moreno JM, Gomez-Ulla F, et al. A 1-year retrospective review of ranibizumab for naive nonsubfoveal choroidal neovascularization secondary to age-related macular degeneration. Retina. 2009; 29:1444–1449.
14. You JY, Chung H, Kim HC. Evaluation of changes in choroidal neovascularization secondary to age-related macular degeneration after anti-VEGF therapy using spectral domain optical coherence tomography. Curr Eye Res. 2012; 37:438–445.
15. CATT Research Group. Martin DF, Maguire MG, et al. Ranibizumab and bevacizumab for neovascular age-related macular degeneration. N Engl J Med. 2011; 364:1897–1908.
16. Dadgostar H, Ventura AA, Chung JY, et al. Evaluation of injection frequency and visual acuity outcomes for ranibizumab monotherapy in exudative age-related macular degeneration. Ophthalmology. 2009; 116:1740–1747.
17. Comparison of Age-related Macular Degeneration Treatments Trials (CATT) Research Group. Martin DF, Maguire MG, et al. Ranibizumab and bevacizumab for treatment of neovascular age-related macular degeneration: two-year results. Ophthalmology. 2012; 119:1388–1398.
Full Text Links
  • KJO
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr