Muscle biopsies in clinical trials for Duchenne muscular dystrophy - Patients' and caregivers' perspective

被引:15
|
作者
Verhaart, Ingrid E. C. [1 ,2 ]
Johnson, Alex [3 ]
Thakrar, Sejal [3 ]
Vroom, Elizabeth [1 ]
De Angelis, Fernando [4 ]
Muntoni, Francesco [5 ,6 ,7 ]
Aartsma-Rus, Annemieke M. [2 ]
Niks, Erik H. [8 ]
机构
[1] Duchenne Parent Project Netherlands, Veenendaal, Netherlands
[2] Leiden Univ, Med Ctr, Dept Human Genet, Leiden, Netherlands
[3] Duchenne UK, London, England
[4] Parent Project Onlus, Rome, Italy
[5] UCL, Great Ormond St Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England
[6] UCL, NIHR Great Ormond St Hosp, Biomed Res Ctr, Great Ormond St Inst Child Hlth, London, England
[7] Great Ormond St Hosp Trust, London, England
[8] Leiden Univ, Dept Neurol, Med Ctr, Leiden, Netherlands
关键词
Clinical trials; Duchenne muscular dystrophy; Muscle biopsy; Patient perspective; Scarring; ANTISENSE OLIGONUCLEOTIDE; RESTORATION; DRISAPERSEN; ANESTHESIA; THERAPY; PHASE-2;
D O I
10.1016/j.nmd.2019.06.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The number of clinical trials for Duchenne muscular dystrophy is increasing. Many trials require muscle biopsies, which involve an invasive surgical procedure. Little is known about short- and long-term impacts of muscle biopsies as perceived by patients and caregivers. Therefore a survey was held among patients and their caregivers who participated in trials involving muscle biopsies, in seven countries. Seventy-eight responses were received. Analysis revealed that many patients and parents had significant anxiety before the biopsy. The main concern of caregivers was the required general anaesthesia. In most cases biopsies caused pain and temporarily hampered daily activities. The main long-term impact was scarring, although large variation in size was reported. Seventy-nine percent of caregivers were little bothered and 21% were moderately or severely bothered by the scar. Willingness to consider another biopsy in future protocols was higher for open-label studies than for placebo-controlled trials. Caregivers stressed the importance of knowing the results of biopsy analyses; only a minority actually received this information. Recommendations are made on the informed consent procedure regarding risks and consequences of muscle biopsies, and communication of results. Furthermore, efforts should be made to minimise the impact of biopsies through pain management and by considering plastic surgery. (C) 2019 The Authors. Published by Elsevier B.V.
引用
收藏
页码:576 / 584
页数:9
相关论文
共 50 条
  • [21] Microdystrophin Expression as a Surrogate Endpoint for Duchenne Muscular Dystrophy Clinical Trials
    Chamberlain, Jeffrey S. S.
    Robb, Melissa
    Braun, Serge
    Brown, Kristy J. J.
    Danos, Olivier
    Ganot, Annie
    Gonzalez-Alegre, Pedro
    Hunter, Nina
    McDonald, Craig
    Morris, Carl
    Tobolowsky, Mark
    Wagner, Kathryn R. R.
    Ziolkowski, Olivia
    Duan, Dongsheng
    HUMAN GENE THERAPY, 2023, 34 (9-10) : 404 - 415
  • [22] Cell Therapy in Duchenne Muscular Dystrophy Treatment: Clinical Trials Overview
    Bajek, Anna
    Porowinska, Dorota
    Kloskowski, Tomasz
    Brzoska, Edyta
    Ciemerych, Maria A.
    Drewa, Tomasz
    CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2015, 25 (01): : 1 - 11
  • [23] Steroids in Duchenne muscular dystrophy: from clinical trials to genomic research
    Muntoni, F
    Fisher, I
    Morgan, JE
    Abraham, D
    NEUROMUSCULAR DISORDERS, 2002, 12 : S162 - S165
  • [24] Expectations and Decision Making in Clinical Trials for Duchenne and Becker Muscular Dystrophy
    Peay, H. L.
    Sheffer, H.
    Tibben, A.
    ANNALS OF NEUROLOGY, 2013, 74 : S184 - S184
  • [25] Dystrophin as a biochemical outcome measure in Duchenne muscular dystrophy clinical trials
    Sardone, V.
    Ellis, M.
    Torelli, S.
    Feng, L.
    Chambers, D.
    Ricotti, V.
    Domingos, J. Pisco
    Phadke, R.
    Sewry, C. A.
    Morgan, J.
    Muntoni, F.
    NEUROMUSCULAR DISORDERS, 2016, 26 : S16 - S16
  • [26] INSPIRATORY MUSCLE TRAINING IN PATIENTS WITH DUCHENNE MUSCULAR-DYSTROPHY
    WANKE, T
    TOIFL, K
    MERKLE, M
    FORMANEK, D
    LAHRMANN, H
    ZWICK, H
    CHEST, 1994, 105 (02) : 475 - 482
  • [27] Purine and carnitine metabolism in muscle of patients with Duchenne muscular dystrophy
    Camina, F
    NovoRodriguez, MI
    RodriguezSegade, S
    CastroGago, M
    CLINICA CHIMICA ACTA, 1995, 243 (02) : 151 - 164
  • [28] Evaluation of skeletal muscle DTI in patients with duchenne muscular dystrophy
    Hooijmans, M. T.
    Damon, B. M.
    Froeling, M.
    Versluis, M. J.
    Burakiewicz, J.
    Verschuuren, J. J. G. M.
    Niks, E. H.
    Webb, A. G.
    Kan, H. E.
    NMR IN BIOMEDICINE, 2015, 28 (11) : 1589 - 1597
  • [29] Assessment of Treatment Effect With Multiple Outcomes in 2 Clinical Trials of Patients With Duchenne Muscular Dystrophy
    Li, Daniel
    McDonald, Craig M.
    Elfring, Gary L.
    Souza, Marcio
    McIntosh, Joseph
    Kim, Dae Hyun
    Wei, Lee-Jen
    JAMA NETWORK OPEN, 2020, 3 (02)
  • [30] The incidence of revertant and trace dystrophin expression in muscle biopsies of Duchenne Muscular Dystrophy patients with different exon deletions
    Lourbakos, A.
    Sipkens, J.
    Beekman, C.
    Kreuger, D.
    Brasz, L.
    Janson, A.
    Campion, G.
    van Deutekom, J.
    de Kipme, S.
    NEUROMUSCULAR DISORDERS, 2011, 21 (9-10) : 643 - 643