Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
10 2020
Historique:
received: 21 04 2020
revised: 30 06 2020
accepted: 01 07 2020
entrez: 20 10 2020
pubmed: 21 10 2020
medline: 15 5 2021
Statut: ppublish

Résumé

Molecular diagnostics of inherited platelet disorders (IPD) has been revolutionized by the implementation of high-throughput sequencing (HTS) approaches. A conclusive diagnosis using HTS tests can be obtained quickly and cost-effectively in many, but not all patients. The expanding use of HTS tests has raised concerns regarding complex variant interpretation and the ethical implications of detecting unsolicited findings such as variants in IPD genes RUNX1, ETV6, and ANKRD26, which are associated with increased leukemic risk. This guidance document has been developed and written by a multidisciplinary team of researchers and clinicians, with expertise in hematology, clinical and molecular genetics, and bioethics, alongside a RUNX1 patient advocacy representative. We recommend that for clinical diagnostics, HTS for IPD should use a multigene panel of curated diagnostic-grade genes. Critically, we advise that an HTS test for clinical diagnostics should only be ordered by a clinical expert that is: (a) fully aware of the complexity of genotype-phenotype correlations for IPD; (b) able to discuss these complexities with a patient and family members before the test is initiated; and (c) able to interpret and appropriately communicate the results of a HTS diagnostic report, including the implication of variants of uncertain clinical significance. Each patient should know what an HTS test could mean for his or her clinical management before initiating a test. We hereby propose an exemplified informed consent document that includes information on these ethical concerns and can be used by the community for implementation of HTS of IPD in a clinical diagnostic setting. This paper does not include recommendations for HTS of IPD in a research setting.

Identifiants

pubmed: 33079472
doi: 10.1111/jth.14993
pmc: PMC7589386
pii: S1538-7836(22)01169-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2751-2758

Informations de copyright

© 2020 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.

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Auteurs

Kate Downes (K)

East Genomic Laboratory Hub, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.

Pascal Borry (P)

Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.

Katrin Ericson (K)

The RUNX1 Research Program, Santa Barbara, CA, USA.

Keith Gomez (K)

Haemophilia Centre and Thrombosis Unit, Royal Free London NHS Foundation Trust, London, UK.

Andreas Greinacher (A)

Institut für Immunologie und Transfusionsmedizin, Universitätsmedizin Greifswald, Greifswald, Germany.

Michele Lambert (M)

Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

Eva Leinoe (E)

Department of Haematology, Rigshospitalet, National University Hospital, Copenhagen, Denmark.

Patrizia Noris (P)

IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.

Chris Van Geet (C)

Department of Cardiovascular Sciences, Center or Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.

Kathleen Freson (K)

Department of Cardiovascular Sciences, Center or Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.

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