Abstract

The growing understanding of the use of biomarkers in Alzheimer's disease (AD) may enable physicians to make more accurate and timely diagnoses. Florbetaben, a beta-amyloid tracer used with positron emission tomography (PET), is one of these diagnostic biomarkers. This analysis was undertaken to explore the potential value of florbetaben PET in the diagnosis of AD among patients with suspected dementia and to identify key data that are needed to further substantiate its value. A discrete event simulation was developed to conduct exploratory analyses from both US payer and societal perspectives. The model simulates the lifetime course of disease progression for individuals, evaluating the impact of their patient management from initial diagnostic work-up to final diagnosis. Model inputs were obtained from specific analyses of a large longitudinal dataset from the New England Veterans Healthcare System and supplemented with data from public data sources and assumptions. The analyses indicate that florbetaben PET has the potential to improve patient outcomes and reduce costs under certain scenarios. Key data on the use of florbetaben PET, such as its influence on time to confirmation of final diagnosis, treatment uptake, and treatment persistency, are unavailable and would be required to confirm its value.

Highlights

  • Alzheimer’s disease (AD) is a fatal and progressive neurodegenerative disorder that affects millions of people worldwide [1]

  • The analyses indicate that florbetaben positron emission tomography (PET) has the potential to improve patient outcomes and reduce costs under certain scenarios

  • With the baby-boomer generation aging, the economic and humanistic burdens caused by AD are expected to grow considerably if effective interventions cannot be discovered in time

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Summary

Introduction

Alzheimer’s disease (AD) is a fatal and progressive neurodegenerative disorder that affects millions of people worldwide [1]. It is currently the sixth leading cause of death in the United States (US), with about 80,000 deaths associated with AD in 2009 [2], and has imposed substantial burden on patients, their caregivers, medical care payers, and society as a whole [3]. Cholinesterase inhibitors and memantine are the only major pharmacological treatments currently available to slow the symptoms associated with disease progression. Clinical studies have demonstrated modest benefits of these treatments in improving the symptoms related to AD [4, 5].

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