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Published on: February 4, 2021
Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs
Nancy Cross1, Cécile van Steen2, Yasmina Zegaoui1
1Market Access, Lightning Health, London, England, UK.
Insights
Retinitis Pigmentosa (RP) causes progressive vision loss, impacting over a million worldwide. Current treatments offer limited options, highlighting the urgent need for innovative therapies and improved patient care guidance.
Area of Science:
- Ophthalmology
- Genetics
- Public Health
Background:
- Retinitis Pigmentosa (RP) is a leading cause of inherited visual impairment and blindness in individuals under 60.
- RP significantly impacts patients' daily lives, employment, independence, and quality of life, exceeding the burden of other retinal conditions.
- The disease imposes substantial psychological and financial stress on patients and their caregivers.
Purpose of the Study:
- To describe the current therapeutic landscape for Retinitis Pigmentosa.
- To assess the disease burden of RP on patients, caregivers, and society.
- To identify gaps and needs in RP diagnosis, treatment, and care.
Main Methods:
- A multi-stage review process including literature searches of public information and systematic reviews (Medline, Embase, Cochrane Library, GlobalData).
- Qualitative research involving senior physicians treating RP patients in the EU and UK.
- Analysis of epidemiological data and cost of RP.
Main Results:
- The therapeutic options for RP are limited, with only one curative gene therapy (voretigene neparvovec) available for a small percentage (1-6%) of patients.
- RP affects over a million people globally, causing significant disability and reduced quality of life.
- There is a lack of comprehensive clinical guidance for managing RP, despite its high disease burden.
Conclusions:
- Retinitis Pigmentosa presents a significant global health challenge with a substantial disease burden and limited therapeutic interventions.
- Effective disease management strategies focus on coping mechanisms, but do not alter the progressive course of RP.
- Development of innovative therapies, coupled with clear clinical guidance, is crucial to transform the treatment landscape for RP patients.
Abstract:
Retinitis Pigmentosa (RP), a group of inherited retinal dystrophies characterised by progressive vision loss, is the leading cause of visual disability and blindness in subjects less than 60 years old. Currently incurable, therapy is aimed at restricting degeneration of vision, treating complications, and helping patients to cope with the psychosocial impact of their disease. Hence, RP is associated with a high burden of disease. This paper describes the current therapeutic landscape for RP and the disease burden for patients, caregivers, and society. A review of available data was conducted in three stages: (1) a literature search of publicly available information on all domains of RP; (2) a systematic literature review using Medline, Embase, the Cochrane Library and grey literature (GlobalData) on epidemiology and cost of RP; and (3) qualitative research with senior physicians treating RP patients in the EU4 and the UK to validate research findings from secondary sources. RP severely impacts the daily lives of over a million people worldwide. Progressive vision loss significantly affects the ability to perform basic daily tasks, to maintain employment, and maintain independence. Consequently, most patients will experience reduced quality of life, with a greater emotional and psychological impact than other conditions related to vision loss such as diabetic retinopathy or age-related macular degeneration. RP is also associated with a high level of carer burden, arising from psychological and financial stress. The therapeutic landscape for RP is limited, with few treatment options and minimal guidance for the diagnosis, treatment, and care of patients. A curative intervention, voretigene neparvovec (Luxturna®), only exists for 1-6% of patients. Although disease management can be successful in developing coping strategies, most patients live with this chronic, progressive condition without interventions to change the disease course. Innovative new therapies can transform the therapeutic landscape, provided appropriate clinical guidance is forthcoming.
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