Biclonal lymphoproliferative disorders: another association with NOTCH1-mutated chronic lymphocytic leukaemias.

Biclonal lymphoproliferative disorder Chronic lymphocytic leukaemia NOTCH1 mutation Richter’s transformation

Journal

Irish journal of medical science
ISSN: 1863-4362
Titre abrégé: Ir J Med Sci
Pays: Ireland
ID NLM: 7806864

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 09 08 2019
accepted: 23 09 2020
pubmed: 18 10 2020
medline: 5 10 2021
entrez: 17 10 2020
Statut: ppublish

Résumé

Biclonal lymphoid disorders, when two distinct lymphoproliferative disorders (LPD) co-exist, are rare (incidence of 1.4%) and associated with a poor prognosis. NOTCH1 mutations occur in 10% of CLL at diagnosis, associated with a short disease-free interval and increased risk of Richter's transformation. We hypothesised that the incidence of NOTCH1 mutations in CLL with a second LPD may be increased, because the mutation occurs early in leukaemogenesis, permitting clonal divergence. We identified 19 patients with biclonal LPD at diagnosis: 11 with CLL and a second LPD (group A) and 8 with a second distinct CLL (group B). NOTCH1 mutation analysis was performed and clinical outcome investigated. Ten of 19 (52%) were NOTCH1 mutated: 5 in group A (45%) and 5 in group B (62.5%) with a favourable clinical outcome observed among this cohort with 28.7 (range 1-99) months of follow-up. In conclusion, we identified a significant (52%) incidence of NOTCH1 mutations in CLL in the context of biclonal LPD, associated with an indolent clinical course.

Identifiants

pubmed: 33068240
doi: 10.1007/s11845-020-02386-1
pii: 10.1007/s11845-020-02386-1
doi:

Substances chimiques

NOTCH1 protein, human 0
Receptor, Notch1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1087-1094

Informations de copyright

© 2020. Royal Academy of Medicine in Ireland.

Références

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Auteurs

Helen Fogarty (H)

Department of Cancer Molecular Diagnostics, St. James's Hospital, Dublin, Ireland. fogarthm@tcd.ie.
Department of Haematology, St James's Hospital and Trinity College, Dublin, Ireland. fogarthm@tcd.ie.
Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, 123 St Stephen's Green, Dublin 2, Ireland. fogarthm@tcd.ie.

Anita Dowling (A)

Department of Cancer Molecular Diagnostics, St. James's Hospital, Dublin, Ireland.
Department of Haematology, St James's Hospital and Trinity College, Dublin, Ireland.

David O'Brien (D)

Department of Haematology, St James's Hospital and Trinity College, Dublin, Ireland.

Steve Langabeer (S)

Department of Cancer Molecular Diagnostics, St. James's Hospital, Dublin, Ireland.

Christopher Laurence Bacon (CL)

Department of Haematology, St James's Hospital and Trinity College, Dublin, Ireland.

Richard Flavin (R)

Department of Pathology, St James's Hospital, Dublin, Ireland.

Michael O'Dwyer (M)

Department of Haematology, Galway Clinic, Galway, Ireland.

Brian Hennessy (B)

Department of Haematology, Waterford University Hospital, Waterford, Ireland.

Hilary O'Leary (H)

Department of Haematology, Limerick University Hospital, Limerick, Ireland.

Gerard Crotty (G)

Department of Haematology, Midlands Regional Hospital, Tullamore, Ireland.

Robert Henderson (R)

Department of Haematology, Midlands Regional Hospital, Tullamore, Ireland.

James Nolan (J)

Department of Haematology, Limerick University Hospital, Limerick, Ireland.

Patrick Thornton (P)

Department of Haematology, Beaumont Hospital, Dublin, Ireland.

Elisabeth Vandenberghe (E)

Department of Cancer Molecular Diagnostics, St. James's Hospital, Dublin, Ireland.
Department of Haematology, St James's Hospital and Trinity College, Dublin, Ireland.

Fiona Quinn (F)

Department of Cancer Molecular Diagnostics, St. James's Hospital, Dublin, Ireland.

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