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Article

An Updated Cost-Utility Model for Onasemnogene Abeparvovec (Zolgensma®) in Spinal Muscular Atrophy Type 1 Patients and Comparison with Evaluation by the Institute for Clinical and Effectiveness Review (ICER)

by
Rebecca Dean
1,
Ivar Jensen
1,
Phil Cyr
1,
Beckley Miller
1,
Benit Maru
2,
Douglas M. Sproule
3,
Douglas E. Feltner
3,
Thomas Wiesner
4,
Daniel C. Malone
5,
Matthias Bischof
3,
Walter Toro
3 and
Omar Dabbous
3,*
1
HEOR, Precision Xtract, Boston, MA, USA
2
Medical Consulting, SSI Strategy, London, UK
3
Global HEOR & RWE, Novartis Gene Therapies, Bannockburn, IL, USA
4
Business Consulting, SSI Strategy, Parsippany, NJ, USA
5
Department of Pharmacotherapy, College of Pharmacy, University of Utah, Salt Lake City, UT, USA
*
Author to whom correspondence should be addressed.
J. Mark. Access Health Policy 2021, 9(1), 1889841; https://doi.org/10.1080/20016689.2021.1889841
Submission received: 11 September 2020 / Revised: 3 February 2021 / Accepted: 9 February 2021 / Published: 28 February 2021

Abstract

Background: Recent cost-utility analysis (CUA) models for onasemnogene abeparvovec (Zolgensma®, formerly AVXS-101) in spinal muscular atrophy type 1 (SMA1) differ on key assumptions and results. Objective: To compare the manufacturer’s proprietary CUA model to the model published by the Institute for Clinical and Economic Review (ICER), and to update the manufacturer’s model with long-term follow-up data and some key ICER assumptions. Study design: We updated a recent CUA evaluating value for money in cost per incremental Quality-adjusted Life Year (QALY) of onasemnogene abeparvovec versus nusinersen (Spinraza®) or best supportive care (BSC) in symptomatic SMA1 patients, and compared it to the ICER model. Setting/Perspective: USA/Commercial payer. Participants: Children aged <2 years with SMA1. Interventions: Onasemnogene abeparvovec, a single-dose gene replacement therapy, versus nusinersen, an antisense oligonucleotide, versus BSC. Main outcome measure: Incremental-cost effectiveness ratio and value-based price using traditional thresholds for general medicines in the US. Results: Updated survival (undiscounted) predicted by the model was 37.60 years for onasemnogene abeparvovec compared to 12.10 years for nusinersen and 7.27 years for BSC. Updated quality-adjusted survival using ICER’s utility scores and discounted at 3% were 13.33, 2.85, and 1.15 discounted QALYs for onasemnogene abeparvovec, nusinersen, and BSC, respectively. Using estimated net prices, the discounted lifetime cost/patient was $3.93 M for onasemnogene abeparvovec, $4.60 M for nusinersen, and $1.96 M for BSC. The incremental cost per QALY gained for onasemnogene abeparvovec was dominant against nusinersen and $161,648 against BSC. These results broadly align with the results of the ICER model, which predicted a cost per QALY gained of $139,000 compared with nusinersen, and $243,000 compared with BSC (assuming a placeholder price of $2 M for onasemnogene abeparvovec), differences in methodology notwithstanding. Exploratory analyses in presymptomatic patients were similar. Conclusion: This updated CUA model is similar to ICER analyses comparing onasemnogene abeparvovec with nusinersen in the symptomatic and presymptomatic SMA populations. At a list price of $2.125 M, onasemnogene abeparvovec is cost-effective compared to nusinersen for SMA1 patients treated before age 2 years. When compared to BSC, cost per QALY of onasemnogene abeparvovec is higher than commonly used thresholds for therapies in the USA ($150,000 per QALY).
Keywords: cost-effectiveness analysis; gene therapy; spinal muscular atrophy; onasemnogene abeparvovec; cost-utility analysis; nusinersen cost-effectiveness analysis; gene therapy; spinal muscular atrophy; onasemnogene abeparvovec; cost-utility analysis; nusinersen

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MDPI and ACS Style

Dean, R.; Jensen, I.; Cyr, P.; Miller, B.; Maru, B.; Sproule, D.M.; Feltner, D.E.; Wiesner, T.; Malone, D.C.; Bischof, M.; et al. An Updated Cost-Utility Model for Onasemnogene Abeparvovec (Zolgensma®) in Spinal Muscular Atrophy Type 1 Patients and Comparison with Evaluation by the Institute for Clinical and Effectiveness Review (ICER). J. Mark. Access Health Policy 2021, 9, 1889841. https://doi.org/10.1080/20016689.2021.1889841

AMA Style

Dean R, Jensen I, Cyr P, Miller B, Maru B, Sproule DM, Feltner DE, Wiesner T, Malone DC, Bischof M, et al. An Updated Cost-Utility Model for Onasemnogene Abeparvovec (Zolgensma®) in Spinal Muscular Atrophy Type 1 Patients and Comparison with Evaluation by the Institute for Clinical and Effectiveness Review (ICER). Journal of Market Access & Health Policy. 2021; 9(1):1889841. https://doi.org/10.1080/20016689.2021.1889841

Chicago/Turabian Style

Dean, Rebecca, Ivar Jensen, Phil Cyr, Beckley Miller, Benit Maru, Douglas M. Sproule, Douglas E. Feltner, Thomas Wiesner, Daniel C. Malone, Matthias Bischof, and et al. 2021. "An Updated Cost-Utility Model for Onasemnogene Abeparvovec (Zolgensma®) in Spinal Muscular Atrophy Type 1 Patients and Comparison with Evaluation by the Institute for Clinical and Effectiveness Review (ICER)" Journal of Market Access & Health Policy 9, no. 1: 1889841. https://doi.org/10.1080/20016689.2021.1889841

APA Style

Dean, R., Jensen, I., Cyr, P., Miller, B., Maru, B., Sproule, D. M., Feltner, D. E., Wiesner, T., Malone, D. C., Bischof, M., Toro, W., & Dabbous, O. (2021). An Updated Cost-Utility Model for Onasemnogene Abeparvovec (Zolgensma®) in Spinal Muscular Atrophy Type 1 Patients and Comparison with Evaluation by the Institute for Clinical and Effectiveness Review (ICER). Journal of Market Access & Health Policy, 9(1), 1889841. https://doi.org/10.1080/20016689.2021.1889841

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