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Interventions for cisplatin-induced hearing loss in children and adolescents with cancer.
Freyer, David R; Brock, Penelope; Knight, Kristin; Reaman, Gregory; Cabral, Sandra; Robinson, Paula D; Sung, Lillian.
Afiliación
  • Freyer DR; Children's Center for Cancer and Blood Diseases, Children's Hospital Los Angeles, Los Angeles, CA, USA; Departments of Pediatrics and Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Brock P; Department of Haematology and Oncology, Great Ormond Street Hospital, London, UK.
  • Knight K; Division of Pediatric Audiology, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, OR, USA.
  • Reaman G; Division of Oncology, Children's National Health System, Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington DC, USA.
  • Cabral S; Pediatric Oncology Group of Ontario, Toronto, ON, Canada.
  • Robinson PD; Pediatric Oncology Group of Ontario, Toronto, ON, Canada.
  • Sung L; Division of Haematology and Oncology, The Hospital for Sick Children, Toronto, ON, Canada. Electronic address: lillian.sung@sickkids.ca.
Lancet Child Adolesc Health ; 3(8): 578-584, 2019 08.
Article en En | MEDLINE | ID: mdl-31160205
ABSTRACT
The identification of preventive interventions that are safe and effective for cisplatin-induced ototoxicity is important, especially in children because hearing loss can impair speech-language acquisition development. Previous randomised trials assessed systemic drugs such as amifostine, sodium diethyldithiocarbamate or disulfiram, and sodium thiosulfate. Amifostine, sodium diethyldithiocarbamate, and disulfiram did not show hearing preservation. Paediatric trials assessing sodium thiosulfate showed efficacy in terms of hearing protection. The SIOPEL 6 trial consisted solely of patients with localised hepatoblastoma and no effects on survival were shown. In the ACCL0431 trial, which included heterogeneous patients, a post-hoc analysis showed significantly worse overall survival among patients who had disseminated disease receiving sodium thiosulfate than among controls, but not among those with localised disease. Intratympanically administered drugs have mainly been assessed in adults and include N-acetylcysteine and dexamethasone. Inconsistent effects of these drugs were identified but these studies were limited by design, small sample size, and statistical approach. Future studies of systemic drugs will need to consider the measurement of disease outcomes through study design and sample size, and ototoxicity endpoints should be harmonised to enhance comparability between trials.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cisplatino / Ototoxicidad / Neoplasias / Antineoplásicos Tipo de estudio: Clinical_trials Idioma: En Revista: Lancet Child Adolesc Health Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cisplatino / Ototoxicidad / Neoplasias / Antineoplásicos Tipo de estudio: Clinical_trials Idioma: En Revista: Lancet Child Adolesc Health Año: 2019 Tipo del documento: Article