Literature DB >> 35980467

Cost-effectiveness analysis of gene-based therapies for patients with spinal muscular atrophy type I in Australia.

Tianjiao Wang1,2, Paul Scuffham3,4, Joshua Byrnes3,4, Martin Downes3,4.   

Abstract

INTRODUCTION: Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder and regarded as one of the most frequent genetic causes of infant mortality. The aim of this study is to develop a cost-effectiveness analysis of AVXS-101 (Onasemnogene Abeparvovec/Zolgensma®) and nusinersen (Spinraza®) for SMA to inform decision-making on reimbursement policies in Australia.
METHODS: A Markov model was developed with five health states to evaluate the costs and effects for patients with SMA Type I from a healthcare system perspective over a time-horizon of 100 years. The model parameters were based on clinical trials, parametric distributions, published literature, and Australian registries. One-way and probabilistic sensitivity analysis were performed to appraise the uncertainties of the parameters in the model. A threshold analysis was conducted to estimate the cost of AVXS-101 of being cost-effective.
RESULTS: The incremental cost-effectiveness ratio (ICER) of AVXS-101 was $1,808,471 per quality-adjusted life year (QALY) and that of nusinersen was $2,772,798 per QALY, compared to standard of care, respectively. The ICER of AVXS-101 was $1,238,288 per QALY compared to nusinersen. The key drivers influencing on ICERs were costs of using treatments and utility values of sitting and walking independently.
CONCLUSION: Both nusinersen and AVXS-101 resulted in health benefits, but they were not cost-effective with a commonly used willingness-to-pay (WTP) threshold of $50,000 per QALY. Developing high-quality clinical data and exploring appropriate WTP thresholds are critical for decision-making on reimbursement policies in the treatment of rare diseases.
© 2022. The Author(s).

Entities:  

Keywords:  Cost-effectiveness analysis; Genetic therapy; Nusinersen; Onasemnogene abeparvovec; Rare disease; Spinal muscular atrophy

Year:  2022        PMID: 35980467     DOI: 10.1007/s00415-022-11319-0

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   6.682


  30 in total

1.  Cost Effectiveness of Nusinersen in the Treatment of Patients with Infantile-Onset and Later-Onset Spinal Muscular Atrophy in Sweden.

Authors:  Santiago Zuluaga-Sanchez; Megan Teynor; Christopher Knight; Robin Thompson; Thomas Lundqvist; Mats Ekelund; Annabelle Forsmark; Adrian D Vickers; Andrew Lloyd
Journal:  Pharmacoeconomics       Date:  2019-06       Impact factor: 4.981

Review 2.  Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care.

Authors:  Eugenio Mercuri; Richard S Finkel; Francesco Muntoni; Brunhilde Wirth; Jacqueline Montes; Marion Main; Elena S Mazzone; Michael Vitale; Brian Snyder; Susana Quijano-Roy; Enrico Bertini; Rebecca Hurst Davis; Oscar H Meyer; Anita K Simonds; Mary K Schroth; Robert J Graham; Janbernd Kirschner; Susan T Iannaccone; Thomas O Crawford; Simon Woods; Ying Qian; Thomas Sejersen
Journal:  Neuromuscul Disord       Date:  2017-11-23       Impact factor: 4.296

3.  Spinal muscular atrophy: survival pattern and functional status.

Authors:  Brian H Y Chung; Virginia C N Wong; Patrick Ip
Journal:  Pediatrics       Date:  2004-10-18       Impact factor: 7.124

4.  The changing natural history of spinal muscular atrophy type 1.

Authors:  M Oskoui; G Levy; C J Garland; J M Gray; J O'Hagen; D C De Vivo; P Kaufmann
Journal:  Neurology       Date:  2007-11-13       Impact factor: 9.910

5.  New insights on the evolution of the SMN1 and SMN2 region: simulation and meta-analysis for allele and haplotype frequency calculations.

Authors:  Shuji Ogino; Robert B Wilson; Bert Gold
Journal:  Eur J Hum Genet       Date:  2004-12       Impact factor: 4.246

6.  Observational study of spinal muscular atrophy type I and implications for clinical trials.

Authors:  Richard S Finkel; Michael P McDermott; Petra Kaufmann; Basil T Darras; Wendy K Chung; Douglas M Sproule; Peter B Kang; A Reghan Foley; Michelle L Yang; William B Martens; Maryam Oskoui; Allan M Glanzman; Jean Flickinger; Jacqueline Montes; Sally Dunaway; Jessica O'Hagen; Janet Quigley; Susan Riley; Maryjane Benton; Patricia A Ryan; Megan Montgomery; Jonathan Marra; Clifton Gooch; Darryl C De Vivo
Journal:  Neurology       Date:  2014-07-30       Impact factor: 9.910

Review 7.  Spinal muscular atrophy.

Authors:  Mitchell R Lunn; Ching H Wang
Journal:  Lancet       Date:  2008-06-21       Impact factor: 79.321

Review 8.  Spinal muscular atrophy: molecular genetics and diagnostics.

Authors:  Shuji Ogino; Robert B Wilson
Journal:  Expert Rev Mol Diagn       Date:  2004-01       Impact factor: 5.225

9.  Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests.

Authors:  Alison Dalton Archibald; Melanie Jane Smith; Trent Burgess; Katrina Louise Scarff; Justine Elliott; Clare Elizabeth Hunt; Zoe McDonald; Caitlin Barns-Jenkins; Chelsea Holt; Karina Sandoval; Vanessa Siva Kumar; Lisa Ward; Emily Caroline Allen; Sarah Valerie Collis; Shannon Cowie; David Francis; Martin B Delatycki; Eppie Mildred Yiu; R John Massie; Mark Domenic Pertile; Desirée du Sart; Damien Bruno; David J Amor
Journal:  Genet Med       Date:  2017-10-26       Impact factor: 8.822

10.  Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens.

Authors:  Elaine A Sugarman; Narasimhan Nagan; Hui Zhu; Viatcheslav R Akmaev; Zhaoqing Zhou; Elizabeth M Rohlfs; Kerry Flynn; Brant C Hendrickson; Thomas Scholl; Deborah Alexa Sirko-Osadsa; Bernice A Allitto
Journal:  Eur J Hum Genet       Date:  2011-08-03       Impact factor: 4.246

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