Understanding patient and parent/caregiver perceptions on gene therapy in Gaucher disease: an international survey

被引:3
|
作者
Collin-Histed, Tanya [1 ]
Rosenberg, Aviva [1 ]
Hopman, Noortje [2 ]
Pacey, Jessica [2 ]
机构
[1] Int Gaucher Alliance, 8 Silver St, Dursley GL11 4ND, England
[2] 67health, 18 Crucifix Ln, London SE1 3JW, England
关键词
Gaucher disease; Patient survey; Gene therapy; Lysosomal storage disease;
D O I
10.1186/s13023-022-02576-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Gaucher disease is a rare, autosomal recessive genetic disorder. It is caused by a lack of sufficient activity of the lysosomal enzyme known as glucocerebrosidase, which leads to an accumulation of glucocerebroside, a fatty substance, in the spleen, liver, bone marrow, and rarely, the lungs or central nervous system. While there are several treatments available for people with Type 1 Gaucher disease and the visceral aspects of Type 3 Gaucher disease, no cure is present for any type of Gaucher disease. Clinical trials are currently underway to investigate the safety and efficacy of gene therapy in Gaucher disease, which has the potential to become a new type of (curative) treatment in the future. Gene therapy is a relatively new therapeutic approach, and with the desire to keep the community informed about new treatment developments, the International Gaucher Alliance (IGA) set-up a Gaucher disease specific survey to gauge current perceptions. The survey aimed to benchmark understanding of, and the educational needs surrounding, gene therapy among the Gaucher disease community.Body An international, online survey was developed, comprising twelve questions ranging from multiple choice, Likert scale, single tick-box, ranking and open questions. The survey was developed following three patient and caregiver focus groups and underwent review from members of the IGA for readability and accuracy before going live to respondents. The survey was available for two months and shared to audiences via specific Gaucher community channels.Conclusion Over 100 patients and parents/caregivers from the Gaucher disease community completed the survey, including people living with Type 1 Gaucher disease (52.88%), people living with Type 3 Gaucher disease (3.85%), parents/caregivers of people living with Type 1, 2 or 3 Gaucher disease (39.42%), and other (3.85%) who were defined as parents of multiple people with Gaucher disease. The survey uncovered various commonalities in perception of gene therapy among all groups, with large knowledge gaps identified on the mode of action, the usefulness of gene therapy and overall understanding of the therapeutic area. This survey provides an overview of the type of information that could be valuable to the Gaucher disease community when developing educational materials.
引用
收藏
页数:5
相关论文
共 50 条
  • [11] Gene therapy for metachromatic leukodystrophy and Gaucher disease
    Severini, GM
    MINERVA BIOTECNOLOGICA, 1997, 9 (04) : 236 - 241
  • [12] TOWARD GENE-THERAPY FOR GAUCHER DISEASE
    KOHN, DB
    NOLTA, JA
    WEINTHAL, J
    BAHNER, I
    YU, XJ
    LILLEY, J
    CROOKS, GM
    HUMAN GENE THERAPY, 1991, 2 (02) : 101 - 105
  • [13] Parents' and caregivers' perceptions of the school climate: development and validation of the Parent and Caregiver Survey (PaCS)
    Aldridge, Jill M.
    McChesney, Katrina
    LEARNING ENVIRONMENTS RESEARCH, 2021, 24 (01) : 23 - 41
  • [14] Parents’ and caregivers’ perceptions of the school climate: development and validation of the Parent and Caregiver Survey (PaCS)
    Jill M. Aldridge
    Katrina McChesney
    Learning Environments Research, 2021, 24 : 23 - 41
  • [15] GENE-THERAPY FOR GAUCHER DISEASE - GLUCOCEREBROSIDASE GENE TRANSDUCTION OF GAUCHER MARROW BY RETROVIRAL VECTORS
    KOHN, DB
    NOLTA, JA
    YU, XJ
    HANLEY, MB
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 231 - 231
  • [16] Intravenously Administered Gene Therapy for Neuronopathic Gaucher Disease
    Massaro, Giulia
    Perocheau, Dany
    Cuka, Sam
    Hughes, Michael
    Baker, Rob
    Karlsson, Stefan
    Chen, Seng
    Waddington, Simon
    Rahim, Ahad
    MOLECULAR THERAPY, 2018, 26 (05) : 399 - 399
  • [17] Enzyme replacement and gene therapy for Gaucher's disease
    Brady, RO
    Barton, NW
    LIPIDS, 1996, 31 : S137 - S139
  • [18] Intravenously administered gene therapy for Neuronopathic Gaucher disease
    Massaro, Giulia
    Perocheau, Dany
    Cuka, Sam
    Hughes, Michael
    Karlsson, Stefan
    Cheng, Seng
    Waddington, Simon
    Rahim, Ahad
    HUMAN GENE THERAPY, 2018, 29 (07) : A2 - A3
  • [19] EVALUATION OF THE POTENTIAL OF GENE-THERAPY FOR GAUCHER DISEASE
    BARRANGER, JA
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 228 - 228
  • [20] Fetal Gene Therapy for Acute Neuronopathic Gaucher Disease
    Rahim, Ahad A.
    Wong, Andrew M.
    Buckley, Suzanne M.
    Hughes, Derralynn A.
    Karlsson, Stefan
    Cooper, Jonathan D.
    Thrasher, Adrian J.
    Mehta, Atul
    Waddington, Simon N.
    MOLECULAR THERAPY, 2009, 17 : S357 - S357