Literature DB >> 31056304

Evaluating Benefit-risk Decision-making in Spinal Muscular Atrophy: A First-ever Study to Assess Risk Tolerance in the SMA Patient Community.

Rosángel Cruz1, Lisa Belter2, Mike Wasnock3, Al Nazarelli3, Jill Jarecki2.   

Abstract

PURPOSE: Patients' perceptions of benefit-risk are essential to informing the regulatory process and the context in which potential therapies are evaluated. To bring this critical information to regulators, Cure SMA launched a first-ever Benefit-Risk Survey for spinal muscular atrophy (SMA) to characterize decision-making and benefit-risk trade-offs in SMA associated with a potential therapy. We hypothesized that risk tolerance would be correlated with SMA type/severity and disease progression. This article presents the results of a benefit-risk survey to enhance understanding of how patients with SMA and caregivers evaluate specific benefits and risks associated with potential therapies.
METHODS: Affected adults, representing all SMA types (I-IV) within the Cure SMA database, and caregivers of affected individuals of all ages/types were invited via e-mail to participate. Best-worst scaling (BWS) was used to assess participants' priorities on benefit-risk trade-offs, as it provides higher discrimination and importance scaling among tested attributes. Twelve potentially clinically meaningful treatment benefits and 11 potential risks (ranging in severity and immediacy) were tested. Multiple factors were correlated with individual responses, including: SMA type/disease severity, stage of disease, respondent type, sex, and quality of life/level of independence (current and expected). Survey respondents were also evaluated for "risk-taking attitudes."
FINDINGS: A total of 298 responses were evaluated (28% affected adults and 72% caregivers, mostly parents). Most respondents were diagnosed >5 years ago (67.3%), with 22.1% SMA type I, 45.6% SMA type II, and 27.9% SMA type III. No strong correlation was found between risk tolerance and SMA type, stage of disease progression, respondent type, sex, quality of life assessment, or rated levels of independence. Irrespective of SMA type, respondents consistently rated the following risks, associated with a potential treatment, as "least tolerable": life-threatening allergic reactions; 1 in 1000 risk of life-threatening side effects leading to possible organ failure; or worsening quality of life. Furthermore, all SMA type respondents rated these risks as "most tolerable": invasive mode of treatment administration (including need for general anesthesia); side effect of dizziness; and other common side effects such as nausea, vomiting, loss of appetite, headaches, back pain, or fatigue. IMPLICATIONS: With the approval of the first SMA treatment, these findings offer a unique opportunity to assess and characterize baseline risk-tolerance in SMA against which to evaluate future SMA treatment options. Although differences had been expected in risk tolerance among respondents based on disease baseline and certain patient attributes, this was not observed. Survey results should inform future SMA drug development and benefit-risk assessments.
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  benefit–risk assessment; best-worst scaling; drug development; patients and caregivers; rare disease; risk tolerance; spinal muscular atrophy (SMA)

Mesh:

Year:  2019        PMID: 31056304     DOI: 10.1016/j.clinthera.2019.03.012

Source DB:  PubMed          Journal:  Clin Ther        ISSN: 0149-2918            Impact factor:   3.393


  10 in total

1.  Experiences of caregivers of children with spinal muscular atrophy participating in the expanded access program for nusinersen: a longitudinal qualitative study.

Authors:  Petra Kiefer; Janbernd Kirschner; Astrid Pechmann; Thorsten Langer
Journal:  Orphanet J Rare Dis       Date:  2020-07-29       Impact factor: 4.123

Review 2.  The SMA Clinical Trial Readiness Program: creation and evaluation of a program to enhance SMA trial readiness in the United States.

Authors:  Ilse Peterson; Rosángel Cruz; Fatou Sarr; Ann Marie Stanley; Jill Jarecki
Journal:  Orphanet J Rare Dis       Date:  2020-05-22       Impact factor: 4.123

3.  Treatment preference among patients with spinal muscular atrophy (SMA): a discrete choice experiment.

Authors:  Alisha Monnette; Er Chen; Dongzhe Hong; Alessandra Bazzano; Stacy Dixon; W David Arnold; Lizheng Shi
Journal:  Orphanet J Rare Dis       Date:  2021-01-20       Impact factor: 4.123

4.  Therapeutic decisions under uncertainty for spinal muscular atrophy: The DECISIONS-SMA study protocol.

Authors:  Gustavo Saposnik; Paola Díaz-Abós; Victoria Sánchez-Menéndez; Carmen Álvarez; María Terzaghi; Jorge Maurino; María Brañas-Pampillón; Ignacio Málaga
Journal:  PLoS One       Date:  2022-02-15       Impact factor: 3.240

5.  A Comparison of Caregiver and Patient Preferences for Treating Duchenne Muscular Dystrophy.

Authors:  Norah L Crossnohere; Ryan Fischer; Elizabeth Vroom; Patricia Furlong; John F P Bridges
Journal:  Patient       Date:  2022-03-04       Impact factor: 3.481

6.  Fetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients.

Authors:  Marisa E Schwab; Julia E H Brown; Billie Lianoglou; Chengshi Jin; Patricia C Conroy; Renata C Gallagher; Paul Harmatz; Tippi C MacKenzie
Journal:  Orphanet J Rare Dis       Date:  2022-01-29       Impact factor: 4.123

7.  Therapeutic Decision-Making Under Uncertainty in the Management of Spinal Muscular Atrophy: Results From DECISIONS-SMA Study.

Authors:  Gustavo Saposnik; Ana Camacho; Paola Díaz-Abós; María Brañas-Pampillón; Victoria Sánchez-Menéndez; Rosana Cabello-Moruno; María Terzaghi; Jorge Maurino; Ignacio Málaga
Journal:  Neurol Ther       Date:  2022-06-03

Review 8.  In Search of a Cure: The Development of Therapeutics to Alter the Progression of Spinal Muscular Atrophy.

Authors:  Kristine S Ojala; Emily J Reedich; Christine J DiDonato; Stephen D Meriney
Journal:  Brain Sci       Date:  2021-02-05

9.  Quality of life data for individuals affected by spinal muscular atrophy: a baseline dataset from the Cure SMA Community Update Survey.

Authors:  Lisa Belter; Rosángel Cruz; Jill Jarecki
Journal:  Orphanet J Rare Dis       Date:  2020-08-24       Impact factor: 4.123

10.  Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment Era.

Authors:  Maggie C Walter; Claudia Chiriboga; Tina Duong; Nathalie Goemans; Anna Mayhew; Laëtitia Ouillade; Maryam Oskoui; Ros Quinlivan; Juan F Vázquez-Costa; John Vissing; Laurent Servais
Journal:  J Neuromuscul Dis       Date:  2021
  10 in total

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