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Protocol for a comprehensive prospective cohort study of trio-based whole-genome sequencing for underlying cancer predisposition in paediatric and adolescent patients newly diagnosed with cancer: the PREDICT study.
Fuentes Bolanos, Noemi Auxiliadora; Padhye, Bhavna; Daley, Macabe; Hunter, Jacqueline; Hetherington, Kate; Warby, Meera; Courtney, Eliza; Kirk, Judy; Josephi-Taylor, Sarah; Chen, Yuyan; Alvaro, Frank; Barlow-Stewart, Kristine; Wong-Erasmus, Marie; Barahona, Paulette; Ajuyah, Pamela; Altekoester, Ann-Kristin; Tyrrell, Vanessa J; Lau, Loretta M S; Wakefield, Claire; Sylvester, Dianne; Tucker, Katherine; Pinese, Mark; Dalla Pozza, Luciano; O'Brien, Tracey A.
Afiliação
  • Fuentes Bolanos NA; Kids Cancer Centre, Sydney Children's Hospitals Network Randwick, Randwick, New South Wales, Australia.
  • Padhye B; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
  • Daley M; Cancer Centre for Children, The Children's Hospital at Westmead, Westmead, New South Wales, Australia bhavna.padhye@health.nsw.gov.au.
  • Hunter J; Kids Research, Children's Cancer Research Unit, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Hetherington K; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
  • Warby M; Behavioural Sciences Unit, Kids Cancer Centre, Randwick, New South Wales, Australia.
  • Courtney E; School of Women's and Children's Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Kirk J; School of Women's and Children's Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Josephi-Taylor S; Behavioural Sciences Unit, Sydney Children's Hospital Randwick, Randwick, New South Wales, Australia.
  • Chen Y; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
  • Alvaro F; Hereditary Cancer Centre, Prince of Wales Hospital Nelune Comprehensive Cancer Centre - NCCC, Randwick, New South Wales, Australia.
  • Barlow-Stewart K; Kids Cancer Centre, Sydney Children's Hospitals Network Randwick, Randwick, New South Wales, Australia.
  • Wong-Erasmus M; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
  • Barahona P; Familial Cancer Service, Westmead Hospital, Westmead, New South Wales, Australia.
  • Ajuyah P; Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
  • Altekoester AK; Department of Clinical Genetics, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Tyrrell VJ; Discipline of Genomic Medicine, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
  • Lau LMS; Kids Research, Children's Cancer Research Unit, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Wakefield C; Paediatric Oncology Service, John Hunter Children's Hospital, Hunter Region Mail Centre, New South Wales, Australia.
  • Sylvester D; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
  • Tucker K; Behavioural Sciences Unit, Kids Cancer Centre, Randwick, New South Wales, Australia.
  • Pinese M; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
  • Dalla Pozza L; School of Women's and Children's Health, University of New South Wales, Sydney, New South Wales, Australia.
  • O'Brien TA; Children's Cancer Institute, Lowy Cancer Centre, UNSW, Randwick, New South Wales, Australia.
BMJ Open ; 13(5): e070082, 2023 05 30.
Article em En | MEDLINE | ID: mdl-37253493
ABSTRACT

INTRODUCTION:

Identifying an underlying germline cancer predisposition (CP) in a child with cancer has potentially significant implications for both the child and biological relatives. Cohort studies indicate that 10%-15% of paediatric cancer patients carry germline pathogenic or likely pathogenic variants in cancer predisposition genes, but many of these patients do not meet current clinical criteria for genetic testing. This suggests broad tumour agnostic germline testing may benefit paediatric cancer patients. However, the utility and psychosocial impact of this approach remain unknown. We hypothesise that an approach involving trio whole-genome germline sequencing (trio WGS) will identify children and families with an underlying CP in a timely fashion, that the trio design will streamline cancer risk counselling to at-risk relatives if CP was inherited, and that trio testing will not have a negative psychosocial impact on families. METHOD AND

ANALYSIS:

To test this, we present the Cancer PREDisposition In Childhood by Trio sequencing study (PREDICT). This study will assess the clinical utility of trio WGS to identify CP in unselected patients with cancer 21 years or younger in New South Wales, Australia. PREDICT will perform analysis of biological parents to determine heritability and will examine the psychosocial impact of this trio sequencing approach. PREDICT also includes a broad genomics research programme to identify new candidate genes associated with childhood cancer risk. ETHICS AND DISSEMINATION By evaluating the feasibility, utility and psychosocial impact of trio WGS to identify CP in paediatric cancer, PREDICT will inform how such comprehensive testing can be incorporated into a standard of care at diagnosis for all childhood cancer patients. TRIAL REGISTRATION NUMBER NCT04903782.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article