Single gene mutations and prognosis in limited-stage follicular lymphoma treated with radiation therapy.

genetics non‐Hodgkin lymphoma prognostic factors radiotherapy

Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
07 Aug 2024
Historique:
received: 14 05 2024
accepted: 28 07 2024
medline: 8 8 2024
pubmed: 8 8 2024
entrez: 7 8 2024
Statut: aheadofprint

Résumé

Radiotherapy is routinely used for management of limited-stage follicular lymphoma (FL), yet half of patients ultimately relapse. We hypothesized that the presence of specific gene mutations may predict outcomes. We performed targeted sequencing of a 69-gene panel in 117 limited-stage FL patients treated with radiotherapy and identified recurrently mutated genes. CREBBP was most frequently mutated, and mutated CREBBP was associated with inferior progression-free survival, though not after false discovery rate adjustment. This association failed to validate in an independent cohort. We conclude that recurrent gene mutations do not predict outcomes in this setting. Alternative biomarkers may offer better prognostic insight.

Identifiants

pubmed: 39112220
doi: 10.1111/bjh.19698
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Leukemia and Lymphoma Society of Canada
ID : 513421
Organisme : Hold 'em for Life Oncology Fellowship
ID : N/A

Informations de copyright

© 2024 The Author(s). British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Samantha A Hershenfeld (SA)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Josuha W D Tobin (JWD)

Mater Research University of Queensland, Brisbane, Queensland, Australia.
Department of Haematology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Victoria Shelton (V)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Lourdes Calvente (L)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Katherine Lajkosz (K)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Ting Liu (T)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Marianne Brodtkorb (M)

Department of Oncology, Oslo University Hospital, Oslo, Norway.

Francesco Annibale d'Amore (FA)

Department of Hematology, Aarhus University Hospital, Aarhus, Denmark.

Maja Ludvigsen (M)

Department of Hematology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Tara Baetz (T)

Queen's University, Kingston, Ontario, Canada.

David LeBrun (D)

Department of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.

Nathalie Johnson (N)

Departments of Medicine and Oncology, Jewish General Hospital, Montreal, Quebec, Canada.

Michael Crump (M)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Michael Hong (M)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

John Kuruvilla (J)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Rosemarie Tremblay-LeMay (R)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Michael MacManus (M)

Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.

Richard Tsang (R)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

David C Hodgson (DC)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Maher K Gandhi (MK)

Mater Research University of Queensland, Brisbane, Queensland, Australia.
Department of Haematology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Robert Kridel (R)

Princess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.

Classifications MeSH