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      The potential price and access implications of the cost-utility and budget impact methodologies applied by NICE in England and ICER in the US for a novel gene therapy in Parkinson’s disease

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          ABSTRACT

          Background: NICE in England, and ICER in the US both use cost-utility analyses (CUA) and budget impact analyses (BIA) to assess value for money and affordability, however the thresholds used differ greatly.

          Objective: To perform a cross-country comparison of the results of the CUA and BIA and detail the implications for reimbursed price and volumes, for a novel gene therapy for Parkinson’s disease (PD).

          Methods: A Markov model was built to perform country-specific CUAs and BIAs

          Findings: The US ceiling price identified through CUA is ~ 1.8 times higher than in England (aligning to our previous US/UK price comparison analysis of high-cost drugs). However, the net budget impact corresponding to these price levels would limit number of patients treated in order not to exceed the BIA threshold. Performance-based annuity payments can increase patient access at launch without exceeding the thresholds while reducing payers’ data uncertainty.

          Conclusion: Our cost-utility analysis in PD shows a difference in price potential between the US and England that aligns with what is observed in practice for other high-cost drugs. Furthermore, the budget impact threshold operational in England imposes a greater downwards pressure on price and/or volumes than the one applied by ICER in the US.

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          Most cited references26

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          ACC/AHA statement on cost/value methodology in clinical practice guidelines and performance measures: a report of the American College of Cardiology/American Heart Association Task Force on Performance Measures and Task Force on Practice Guidelines.

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            Progression of Parkinson's disease as evaluated by Hoehn and Yahr stage transition times.

            This study was carried out to evaluate progression in Parkinson's disease (PD) by analyzing time taken to transit from one Hoehn and Yahr (H&Y) stage to the next stage and to investigate the variables that would be associated with H&Y transition times using a large PD database that contained prospectively collected information. Data were obtained from the movement disorder database of the National Neuroscience Institute in Singapore. Kaplan-Meier (KM) survival analysis was adopted to investigate the time taken to progress through various H&Y stages. Cox regression analysis was used to examine the association between the baseline variables at the entry point of each H&Y stage and the progression to the next stage. A total of 695 patients (mean age: 65.2, male: 57.3%) were studied. Using KM analysis, the median time taken to transit from H&Y stage 1 to 2, 2 to 2.5, 2.5 to 3 were 20, 62, and 25 months, respectively; whereas the median time taken to progress from stage 3 to 4 and 4 to 5 were 24 and 26 months, respectively. Cox regression analysis revealed that older age-at-diagnosis, longer PD duration, and higher Unified Parkinson's Disease Rating Scale (UPDRS) motor scores at baseline were associated with a significantly faster progression through various H&Y stages. Gender and ethnicity were not associated with disease progression. In conclusion, H&Y transition time is a useful measure of disease progression in PD and may be utilized in clinical studies evaluating therapeutic interventions and prognostic factors in PD. 2010 Movement Disorder Society
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              Classification of advanced stages of Parkinson’s disease: translation into stratified treatments

              Advanced stages of Parkinson’s disease (advPD) still impose a challenge in terms of classification and related stage-adapted treatment recommendations. Previous concepts that define advPD by certain milestones of motor disability apparently fall short in addressing the increasingly recognized complexity of motor and non-motor symptoms and do not allow to account for the clinical heterogeneity that require more personalized approaches. Therefore, deep phenotyping approaches are required to characterize the broad-scaled, continuous and multidimensional spectrum of disease-related motor and non-motor symptoms and their progression under real-life conditions. This will also facilitate the reasoning for clinical care and therapeutic decisions, as neurologists currently have to refer to clinical trials that provide guidance on a group level; however, this does not always account for the individual needs of patients. Here, we provide an overview on different classifications for advPD that translate into critical phenotypic patterns requiring the differential therapeutic adjustments. New concepts refer to precision medicine approaches also in PD and first studies on genetic stratification for therapeutic outcomes provide a potential for more objective treatment recommendations. We define novel treatment targets that align with this concept and make use of emerging device-based assessments of real-life information on PD symptoms. As these approaches require empowerment of patients and integration into treatment decisions, we present communication strategies and decision support based on new technologies to adjust treatment of advPD according to patient demands and safety.
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                Author and article information

                Journal
                J Mark Access Health Policy
                J Mark Access Health Policy
                ZJMA
                zjma20
                Journal of Market Access & Health Policy
                Routledge
                2001-6689
                2018
                06 August 2018
                : 6
                : 1
                : 1500419
                Affiliations
                [a ]Health Economics and Market Access Department, Cell and Gene Therapy Catapult , London, UK
                [b ]Business Development Department, Oxford BioMedica (UK) , Oxford, UK
                Author notes
                CONTACT Panos Kefalas panos.kefalas@ 123456ct.catapult.org.uk Cell and Gene Therapy Catapult , 12th Floor Tower Wing, Guys Hospital, Great Maze Pond, LondonSE1 9RT, UK
                Article
                1500419
                10.1080/20016689.2018.1500419
                6198614
                30364868
                465a2e2e-d2a4-4c6b-bd64-e6bfcf5409be
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 April 2018
                : 09 July 2018
                : 04 July 2018
                Page count
                Figures: 6, Tables: 4, References: 68, Pages: 16
                Funding
                Funded by: Oxford BioMedica (UK) Ltd and conducted by the Cell and Gene Therapy Catapult
                Award ID: not applicable
                This study was funded by Oxford BioMedica (UK) Ltd and conducted by the Cell and Gene Therapy Catapult.
                Categories
                Original Research Article

                gene therapy,parkinson’s disease,cost-utility analysis,budget impact analysis,pricing and reimbursement,patient access,england,united kingdom (uk)

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