» Articles » PMID: 31100217

Use of Bevacizumab and Ranibizumab for Wet Age-Related Macular Degeneration: Influence of CATT Results and Introduction of Aflibercept

Overview
Journal Am J Ophthalmol
Specialty Ophthalmology
Date 2019 May 18
PMID 31100217
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To assess whether publication of Comparison of Age-related macular degeneration Treatment Trial (CATT) results and introduction of aflibercept to the marketplace affected intravitreal bevacizumab and ranibizumab utilization.

Design: Retrospective analysis of treatment patterns.

Methods: We calculated weekly bevacizumab and ranibizumab utilization during 3 timeframes: (1) before CATT publication, (2) between CATT publication (April 28, 2011) and assignment of a unique aflibercept billing code (January 1, 2013), and (3) afterward for 164,188 Medicare beneficiaries with neovascular macular degeneration receiving ≥1 anti-vascular endothelial growth factor injection(s) from January 1, 2008 to December 31, 2014. We identified ophthalmologists who predominantly (≥80%) administered bevacizumab or ranibizumab and evaluated changes in preferences over the 3 periods. We replicated analyses on 881,381 commercially insured beneficiaries.

Results: Among 317 ophthalmologists administering predominantly ranibizumab to Medicare beneficiaries pre-CATT, 221 (69.7%) reduced ranibizumab use post-CATT, whereas 96 (30.3%) continued using ranibizumab ≥80% of the time. Findings were reversed among 1041 ophthalmologists who predominantly administered bevacizumab pre-CATT-777 (74.6%) continued bevacizumab-predominant use while 264 (25.4%) reduced bevacizumab use post-CATT. Among the 145 ophthalmologists who predominantly administered ranibizumab before aflibercept's availability, 77 (53.1%) reduced ranibizumab utilization and 68 (46.9%) continued using ranibizumab ≥80% of the time after aflibercept became available. Corresponding numbers among the 909 ophthalmologists who predominantly administered bevacizumab pre-aflibercept were 381 (41.9%) reducing and 528 (58.1%) continuing bevacizumab-predominant use. Similar results were observed for commercially insured patients.

Conclusions: Many ophthalmologists who favored ranibizumab switched to bevacizumab after CATT publication, while most who favored bevacizumab before CATT publication continued favoring it afterward. Aflibercept's introduction had little impact on preferences for ranibizumab or bevacizumab.

Citing Articles

Monoclonal Antibodies for the Treatment of Ocular Diseases.

Henriques C, da Ana R, Krambeck K, Miguel S, Santini A, Zielinska A J Clin Med. 2024; 13(19).

PMID: 39407875 PMC: 11482488. DOI: 10.3390/jcm13195815.


The potential effects of newer groups of glucose lowering drugs on age-related macular degeneration.

Ebrahimi M, Sivaprasad S Eye (Lond). 2024; 38(13):2649-2650.

PMID: 38605074 PMC: 11383937. DOI: 10.1038/s41433-024-03066-5.


Medicare Part B Spending on Macular Degeneration Treatments Associated With Manufacturer Payments to Ophthalmologists.

Dickson S, James K JAMA Health Forum. 2023; 4(9):e232951.

PMID: 37682553 PMC: 10492178. DOI: 10.1001/jamahealthforum.2023.2951.


Evaluation of macular vascular density and foveal avascular zone changes by optical coherence tomography angiography (OCT-A) after intravitreal dexamethasone implant in diabetic macular edema resistant to Anti-VEGF treatment.

Ceylan A, Dogan M, Demircan A, Akar Y Int Ophthalmol. 2022; 42(11):3579-3588.

PMID: 35737210 DOI: 10.1007/s10792-022-02374-7.


IQGAP1 causes choroidal neovascularization by sustaining VEGFR2-mediated Rac1 activation.

Wang H, Ramshekar A, Kunz E, Sacks D, Hartnett M Angiogenesis. 2020; 23(4):685-698.

PMID: 32783108 PMC: 7530064. DOI: 10.1007/s10456-020-09740-y.


References
1.
Gower E, Stein J, Shekhawat N, Mikkilineni S, Blachley T, Pajewski N . Geographic and Demographic Variation in Use of Ranibizumab Versus Bevacizumab for Neovascular Age-related Macular Degeneration in the United States. Am J Ophthalmol. 2017; 184:157-166. DOI: 10.1016/j.ajo.2017.10.010. View

2.
Brechner R, Rosenfeld P, Babish J, Caplan S . Pharmacotherapy for neovascular age-related macular degeneration: an analysis of the 100% 2008 medicare fee-for-service part B claims file. Am J Ophthalmol. 2011; 151(5):887-895.e1. DOI: 10.1016/j.ajo.2010.11.017. View

3.
Boissel J . Impact of randomized clinical trials on medical practices. Control Clin Trials. 1989; 10(4 Suppl):120S-134S. DOI: 10.1016/0197-2456(89)90051-2. View

4.
Lenfant C . Shattuck lecture--clinical research to clinical practice--lost in translation?. N Engl J Med. 2003; 349(9):868-74. DOI: 10.1056/NEJMsa035507. View

5.
Parikh R, Ross J, Sangaralingham L, Adelman R, Shah N, Barkmeier A . Trends of Anti-Vascular Endothelial Growth Factor Use in Ophthalmology Among Privately Insured and Medicare Advantage Patients. Ophthalmology. 2016; 124(3):352-358. DOI: 10.1016/j.ophtha.2016.10.036. View