Decision making for health-related research outcomes that alter diagnosis: A model from paediatric brain tumours.

archival studies health‐related findings human tissue molecular pathology paediatric brain tumours

Journal

Neuropathology and applied neurobiology
ISSN: 1365-2990
Titre abrégé: Neuropathol Appl Neurobiol
Pays: England
ID NLM: 7609829

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 10 05 2024
accepted: 20 05 2024
medline: 10 7 2024
pubmed: 10 7 2024
entrez: 10 7 2024
Statut: ppublish

Résumé

The question of how to handle clinically actionable outcomes from retrospective research studies is poorly explored. In neuropathology, this problem is exacerbated by ongoing refinement in tumour classification. We sought to establish a disclosure threshold for potential revised diagnoses as determined by the neuro-oncology speciality. As part of a previous research study, the diagnoses of 73 archival paediatric brain tumour samples were reclassified according to the WHO 2016 guidelines. To determine the disclosure threshold and clinical actionability of pathology-related findings, we conducted a result-evaluation approach within the ethical framework of BRAIN UK using a surrogate clinical multidisciplinary team (MDT) of neuro-oncology specialists. The MDT identified key determinants impacting decision-making, including anticipated changes to patient management, time elapsed since initial diagnosis, likelihood of the patient being alive and absence of additional samples since cohort inception. Ultimately, none of our research findings were considered clinically actionable, largely due to the cohort's historic archival and high-risk nature. From this experience, we developed a decision-making framework to determine if research findings indicating a change in diagnosis require reporting to the relevant clinical teams. Ethical issues relating to the use of archival tissue for research and the potential to identify actionable findings must be carefully considered. We have established a structured framework to assess the actionability of research data relating to patient diagnosis. While our specific findings are most applicable to the pathology of poor prognostic brain tumour groups in children, the model can be adapted to a range of disease settings, for example, other diseases where research is dependent on retrospective tissue cohorts, and research findings may have implications for patients and families, such as other tumour types, epilepsy-related pathology, genetic disorders and degenerative diseases.

Identifiants

pubmed: 38982613
doi: 10.1111/nan.12994
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12994

Subventions

Organisme : Olivia Hodson Cancer Fund
ID : SR16A23
Organisme : Brain Tumour Charity
ID : GN-16/193

Informations de copyright

© 2024 The Author(s). Neuropathology and Applied Neurobiology published by John Wiley & Sons Ltd on behalf of British Neuropathological Society.

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Auteurs

Jessica C Pickles (JC)

Developmental Biology and Cancer & Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Department of Histopathology, NIHR Great Ormond Street Hospital Biomedical Research Centre and UCL, London, UK.

Kristian Aquilina (K)

Department of Paediatric Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Jane Chalker (J)

Specialist Integrated Haematology and Malignancy Diagnostic Service-Acquired Genomics, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Christine Dahl (C)

Department of Paediatric Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Abel Devadass (A)

Beaumont Hospital, Dublin, Ireland.

Kshitij Mankad (K)

Department of Paediatric Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Ashirwad Merve (A)

Department of Histopathology, NIHR Great Ormond Street Hospital Biomedical Research Centre and UCL, London, UK.

Munaza Ahmed (M)

North East Thames Regional Clinical Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

James A R Nicoll (JAR)

Clinical & Experimental Sciences, University of Southampton, Southampton, UK.
Cellular Pathology, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Tabitha Bloom (T)

Clinical & Experimental Sciences, University of Southampton, Southampton, UK.

David A Hilton (DA)

Department of Histopathology, University Hospitals Plymouth, Plymouth, UK.

Neil J Sebire (NJ)

Developmental Biology and Cancer & Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Department of Histopathology, NIHR Great Ormond Street Hospital Biomedical Research Centre and UCL, London, UK.

Darren Hargrave (D)

Developmental Biology and Cancer & Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Department of Paediatric Haematology and Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Thomas S Jacques (TS)

Developmental Biology and Cancer & Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Department of Histopathology, NIHR Great Ormond Street Hospital Biomedical Research Centre and UCL, London, UK.

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