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Published in: Advances in Therapy 3/2020

Open Access 01-03-2020 | Gene Therapy in Oncology | Original Research

An Economic Evaluation of Voretigene Neparvovec for the Treatment of Biallelic RPE65-Mediated Inherited Retinal Dystrophies in the UK

Authors: Daniel Viriato, Natalie Bennett, Raisa Sidhu, Elizabeth Hancock, Hannah Lomax, David Trueman, Robert E. MacLaren

Published in: Advances in Therapy | Issue 3/2020

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Abstract

Introduction

Voretigene neparvovec (VN) is a gene therapy and the first approved pharmacological treatment for biallelic RPE65-mediated inherited retinal dystrophies (IRD), a rare condition that starts in early life and causes vision to progressively deteriorate towards complete blindness. In a phase III trial, treatment with VN significantly improved functional vision and visual function, and in October 2019 the National Institute for Health and Care Excellence (NICE) Highly Specialised Technologies (HST) process recommended VN for patients in England and Wales. We assessed the cost-effectiveness of VN compared with best supportive care (BSC) in individuals with biallelic RPE65-mediated IRD in the UK.

Methods

A Markov model was developed to estimate the incremental cost per quality-adjusted life-year (QALY) gained for VN compared with BSC, from the perspective of the UK National Health Service and Personal Social Services. Phase III trial data were used to inform transition probabilities up to year 1, after which the treatment effect was assumed to be maintained for 40 years, followed by a decline in vision. A bespoke elicitation exercise involving clinical experts, patients and carers was conducted to estimate utility values for each model health state.

Results

At list price, VN is associated with incremental costs of £612,404 and incremental QALYs of 6.4, resulting in an incremental cost-effectiveness ratio (ICER) of £95,072 per QALY gained. Voretigene neparvovec is associated with a significant undiscounted QALY gain (20.5) and is therefore eligible for additional QALY weighting under the NICE HST process; an ICER of up to £205,000 per QALY gained could be considered cost-effective under this framework.

Conclusion

The results of the model show VN to be a cost-effective use of healthcare resources in the UK at list price. The availability of a commercial discount in the UK (as considered in the NICE appraisal) means that in reality the ICER will be even lower.

Plain Language Summary

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Literature
2.
go back to reference Russell S, Bennett J, Wellman JA, Chung DC, Yu Z-F, Tillman A, Wittes J, Pappas J, Elci O, McCague S, Cross D, Marshall KA, Walshire J, Kehoe TL, Reichert H, Davis M, Raffini L, George LA, Hudson FP, Dingfield L, Zhu X, Haller JA, Sohn EH, Mahajan VB, Pfeifer W, Weckmann M, Johnson C, Gewaily D, Drack A, Stone E, Wachtel K, Simonelli F, Leroy BP, Wright JF, High KA, Maguire AM. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial. Lancet. 2017;390:849–60. https://doi.org/10.1016/S0140-6736(17)31868-8.CrossRefPubMedCentralPubMed Russell S, Bennett J, Wellman JA, Chung DC, Yu Z-F, Tillman A, Wittes J, Pappas J, Elci O, McCague S, Cross D, Marshall KA, Walshire J, Kehoe TL, Reichert H, Davis M, Raffini L, George LA, Hudson FP, Dingfield L, Zhu X, Haller JA, Sohn EH, Mahajan VB, Pfeifer W, Weckmann M, Johnson C, Gewaily D, Drack A, Stone E, Wachtel K, Simonelli F, Leroy BP, Wright JF, High KA, Maguire AM. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial. Lancet. 2017;390:849–60. https://​doi.​org/​10.​1016/​S0140-6736(17)31868-8.CrossRefPubMedCentralPubMed
9.
go back to reference Bolat N, Doğangün B, Yavuz M, Demir T, Kayaalp L. Depression and anxiety levels and self-concept characteristics of adolescents with congenital complete visual impairment. Turk Psikiyatri Dergisi Turk J Psychiatry. 2011;22:77–82. Bolat N, Doğangün B, Yavuz M, Demir T, Kayaalp L. Depression and anxiety levels and self-concept characteristics of adolescents with congenital complete visual impairment. Turk Psikiyatri Dergisi Turk J Psychiatry. 2011;22:77–82.
13.
go back to reference Leger D, Guilleminault C, Defrance R, Domont A, Paillard M. Prevalence of sleep/wake disorders in persons with blindness. Clin Sci. 1999;97:193–9 (London, England: 1979).CrossRef Leger D, Guilleminault C, Defrance R, Domont A, Paillard M. Prevalence of sleep/wake disorders in persons with blindness. Clin Sci. 1999;97:193–9 (London, England: 1979).CrossRef
16.
go back to reference Viriato D, Glen F, Bennett N, Aouadj C, Hancock E, Lomax H, Sidhu R. (PSS6) What is the lifetime cost of blindness in people with RPE65-mediated inherited retinal dystrophy in the UK? Value Health. 2019;22(Supplement 3):S886–7.CrossRef Viriato D, Glen F, Bennett N, Aouadj C, Hancock E, Lomax H, Sidhu R. (PSS6) What is the lifetime cost of blindness in people with RPE65-mediated inherited retinal dystrophy in the UK? Value Health. 2019;22(Supplement 3):S886–7.CrossRef
19.
go back to reference Drack AV, Bennett J, Russell S, High KA, Yu Z-F, Tillman A, Chung DC, Reape KZ, Ciulla T, Maguire AM. How long does gene therapy last? 4 Year follow-up of Phase 3 Voretigene Neparvovec Trial in RPE65-associated LCA/inherited retinal disease. J AAPOS. 2019;23(4):e7.CrossRef Drack AV, Bennett J, Russell S, High KA, Yu Z-F, Tillman A, Chung DC, Reape KZ, Ciulla T, Maguire AM. How long does gene therapy last? 4 Year follow-up of Phase 3 Voretigene Neparvovec Trial in RPE65-associated LCA/inherited retinal disease. J AAPOS. 2019;23(4):e7.CrossRef
20.
go back to reference Chung DC, Lee K, Reape KZ, High K, Lacey S, Viriato D. Long-term effect of voretigene neparvovec on the full-field light sensitivity threshold test of patients with RPE65 mutation-associated inherited retinal dystrophy—post hoc analysis of Phase I trial data. Investig Ophthalmol Vis Sci. 2019;60:3398.CrossRef Chung DC, Lee K, Reape KZ, High K, Lacey S, Viriato D. Long-term effect of voretigene neparvovec on the full-field light sensitivity threshold test of patients with RPE65 mutation-associated inherited retinal dystrophy—post hoc analysis of Phase I trial data. Investig Ophthalmol Vis Sci. 2019;60:3398.CrossRef
21.
go back to reference Maguire AM, Russell S, Wellman JA, Chung DC, Yu Z-F, Tillman A, Wittes J, Pappas J, Elci O, Marshall KA, McCague S, Reichert H, Davis M, Simonelli F, Leroy BP, Wright JF, High KA, Bennett J. Efficacy, safety, and durability of voretigene neparvovec-rzyl in RPE65 mutation-associated inherited retinal dystrophy. Ophthalmology. 2019;126(9):1273–85. https://doi.org/10.1016/j.ophtha.2019.06.017.CrossRefPubMed Maguire AM, Russell S, Wellman JA, Chung DC, Yu Z-F, Tillman A, Wittes J, Pappas J, Elci O, Marshall KA, McCague S, Reichert H, Davis M, Simonelli F, Leroy BP, Wright JF, High KA, Bennett J. Efficacy, safety, and durability of voretigene neparvovec-rzyl in RPE65 mutation-associated inherited retinal dystrophy. Ophthalmology. 2019;126(9):1273–85. https://​doi.​org/​10.​1016/​j.​ophtha.​2019.​06.​017.CrossRefPubMed
25.
30.
go back to reference Pastores GB, Hughes J, Rogers Y, Stenson C, Clark A, Lloyd A, Alvarez I, Jain M, Kha A, Monavari A. 262-Estimation of resource use and quality of life in phenylketonuria (PKU) patients in Ireland. J Inborn Errors Metab Screen. 2017;5:118. Pastores GB, Hughes J, Rogers Y, Stenson C, Clark A, Lloyd A, Alvarez I, Jain M, Kha A, Monavari A. 262-Estimation of resource use and quality of life in phenylketonuria (PKU) patients in Ireland. J Inborn Errors Metab Screen. 2017;5:118.
40.
go back to reference Chung DC, Russell SR, Bennett J, Maguire AM, Wellman JA, Yu ZF, Tillman A, High KA. Correlation of multi-luminance mobility testing with visual function tests in a phase 3 trial of voretigene neparvovec for biallelic RPE65-mediated inherited retinal disease. Investig Ophthalmol Vis Sci. 2017;58:3292. Chung DC, Russell SR, Bennett J, Maguire AM, Wellman JA, Yu ZF, Tillman A, High KA. Correlation of multi-luminance mobility testing with visual function tests in a phase 3 trial of voretigene neparvovec for biallelic RPE65-mediated inherited retinal disease. Investig Ophthalmol Vis Sci. 2017;58:3292.
Metadata
Title
An Economic Evaluation of Voretigene Neparvovec for the Treatment of Biallelic RPE65-Mediated Inherited Retinal Dystrophies in the UK
Authors
Daniel Viriato
Natalie Bennett
Raisa Sidhu
Elizabeth Hancock
Hannah Lomax
David Trueman
Robert E. MacLaren
Publication date
01-03-2020
Publisher
Springer Healthcare
Published in
Advances in Therapy / Issue 3/2020
Print ISSN: 0741-238X
Electronic ISSN: 1865-8652
DOI
https://doi.org/10.1007/s12325-020-01243-y

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