Abstract

Ten percent of the Medicare Part B budget is spent on aflibercept, used to treat a myriad of ocular neovascular diseases. A substantial portion of these costs can be attributed to a few hundred ophthalmologists, raising concerns regarding the influence of pharmaceutical companies on the choice of medication by a relatively small group of clinicians. One approach to protect patients' health care interests is to include them in deliberations on the choice of therapy for their eye disease. To examine factors associated with patients' choice between an effective and less expensive off-label drug or a more effective, but also more expensive, US Food and Drug Administration (FDA)-approved drug. This retrospective cohort analysis used data from the satellite office of a tertiary referral center from August 2, 2013, to April 9, 2018. Insured patients initiating treatment with anti-vascular endothelial growth factor were included in the analysis. Data were analyzed from March 26, 2018, to June 10, 2020. Patients were asked to choose between bevacizumab (approximately $100 per dose), a chemotherapy that is effective, but not FDA approved, for the treatment of ocular vascular disease, or aflibercept (approximately $2000 per dose), an FDA-approved drug for ocular vascular disease that may be more effective than bevacizumab in some patients. Independent of this choice, patients were separately asked by a study coordinator to participate in an invasive clinical study for which they would not be compensated, there was a small risk for an adverse event, and they would not personally benefit from participating (a surrogate marker for altruism). Factors associated with patients' choice of medication, including age, sex, ocular disease, race, and participation in an invasive clinical study. A total of 189 patients were included in the analysis (106 women [56%]; mean [SEM] age, 74.6 [0.8] years). Despite being told that it may not be as effective as aflibercept, 100 patients (53%) selected bevacizumab for their own eye care. An act of altruism (ie, participation in an invasive clinical study) when the patient was making a choice between the 2 drugs was associated with a patient's choice of bevacizumab (odds ratio [OR], 7.03; 95% CI, 2.27-21.80; P < .001); the OR for selecting bevacizumab for patients who never agreed to participate in the clinical study was 0.45 (95% CI, 0.25-0.83; P = .001). Age (OR, 1.00; 95% CI, 0.97-1.03; P = .86), race (OR, 0.70; 95% CI, 0.41-1.22; P = .21), sex (OR, 0.72; 95% CI, 0.39-1.35; P = .31), presence of diabetes (OR, 1.52; 95% CI, 0.59-3.93; P = .39), and type of eye disease (OR, 0.56; 95% CI, 0.30-1.04; P = .07) were not associated with choice of therapy. These findings suggest that clinicians must consider the ethical implications of the influence of altruism when patients participate in the decision between cost-effective vs the most effective medicines for their own health care.

Highlights

  • The introduction of therapies targeting vascular endothelial growth factor (VEGF) has had a remarkable effect on the treatment of ocular neovascular disease.[1]

  • An act of altruism when the patient was making a choice between the 2 drugs was associated with a patient’s choice of bevacizumab; the odds ratio (OR) for selecting bevacizumab for patients who never agreed to participate in the clinical study was 0.45

  • Factors Associated With a Patient’s Decision to Select Therapy for Their Own Eye Disease. These findings suggest that clinicians must consider the ethical implications of the influence of altruism when patients participate in the decision between costeffective vs the most effective medicines for their own health care

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Summary

Introduction

The introduction of therapies targeting vascular endothelial growth factor (VEGF) has had a remarkable effect on the treatment of ocular neovascular disease.[1]. In June 2006, a closely related drug, ranibizumab (Lucentis), was approved by the FDA for use in the eye and was priced at approximately $3000 per dose. A third therapy, aflibercept (Eylea), was subsequently approved by the FDA for use in the eye for approximately $2000 per dose. These 3 anti-VEGF therapies are currently used to treat a myriad of ocular diseases, most notably nvAMD, diabetic eye disease, and retinal vein occlusion (RVO)

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