Current regulations discourage the use of the more cost-effective bevacizumab and lead to unequal patient access to higher-cost ranibizumab and aflibercept.
The cost of anti—vascular endothelial growth factor (anti-VEGF) treatments for eye disorders has proven to be a challenge in providing equitable access to patients while controlling treatment costs. A newly published longitudinal study of hospital prescribing costs, set in England’s National Health Service (NHS), sought to describe growth in the use and cost of—as well as patient access to—these agents. The researchers found that current national regulations discourage the use of the more cost-effective bevacizumab and lead to unequal patient access to higher-cost ranibizumab and aflibercept in treating eye conditions.
Clinical commissioning groups (CCGs), which are responsible for commissioning healthcare for local populations in the United Kingdom, in concert with cost-effectiveness criteria established by the National Institute for Health and Care Excellence (NICE), have found that commissioning anti-VEGF medicines for patients with eye conditions has been a unique challenge. Two drugs, ranibizumab and aflibercept, are cleared by NICE to treat neovascular age-related degeneration, diabetic macular edema, retinal vein occlusion, and myopic choroidal neovascularization. The drugs have a per-injection cost to England’s NHS of approximately £550 and £800 (approximately $719 and $1045), respectively.
However, another anti-VEGF agent, bevacizumab, was not evaluated by NICE for the treatment of these conditions. Bevacizumab, which is approved for the treatment of cancer but not of ophthalmological indications, can be divided into smaller doses for ophthalmic therapy, and each injection carries a far lower cost burden at £50 to £100 (approximately $65 to $131). Bevacizumab has been demonstrated to be effective in the treatment of eye diseases, and to be more cost-effective than the 2 NICE-approved treatments.
In the study, William Hollingworth, PhD, and colleagues used Hospital Episode Statistics (HES), which are routinely collected data sets recording all episodes of care in NHS hospitals, and extracted data from hospital prescribing cost reports to estimate the costs of ranibizumab and aflibercept since 2008. The researchers also drew from a 2015 study that estimated prevalence of ranibizumab, aflibercept, and bevacizumab injections for the treatment of eye conditions at 61.1%, 36.0%, and 2.8% of treatments, respectively.
The researchers found that:
Interestingly, not all regions of the United Kingdom shared the same rates of procedures; substantial variation in access to anti-VEGF treatment was present within areas served by the same CCGs; for example, in the areas of Somerset and Wiltshire, relatively high procedure rates were evident near the cities of Bath, Bristol, and Swindon. However, procedure rates were lower in other areas in the same CCGs.
Use of bevacizumab could help to remediate the problem of high costs of and unequal access to these drugs, according to the authors, who point to existing data that suggest the NHS could save £102 million (approximately $133 million) per year by switching from ranibizumab to bevacizumab. Such a switch could help to address the “considerable potential unmet need in some areas of the country.”
The authors conclude that current regulations encourage the increased use of ranibizumab and aflibercept rather than bevacizumab, which could be a more cost-effective alternative. “This limits the ability of NHS to pay for care for other patients,” the authors say, and caution that “NHS patients in England do not have equal access to the most cost-effective care.”
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
Insights from Festival of Biologics: Dracey Poore Discusses Cardinal Health’s 2024 Biosimilar Report
May 19th 2024The discussion highlights key emerging trends from the Festival of Biologics conference and the annual Cardinal Health Biosimilars Report, including the importance of sustainability in the health care landscape and the challenges and successes in biosimilar adoption and affordability.
Samsung Bioepis Report Showcases Adalimumab Biosimilar Growth in Market Share
October 11th 2024Adalimumab biosimilars have seen a significant increase in market share, from 2% in early 2024 to 22%, as payers and pharmacy benefit managers begin to prioritize these biosimilars over the reference product, Humira.