Prognostic impact of pretreatment cell-free DNA concentration in newly diagnosed peripheral T-cell lymphomas.

DNA prognosis T-cell lymphoma haematological malignancies prognostic factors

Journal

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

Informations de publication

Date de publication:
04 Jan 2024
Historique:
revised: 14 12 2023
received: 03 10 2023
accepted: 19 12 2023
medline: 5 1 2024
pubmed: 5 1 2024
entrez: 4 1 2024
Statut: aheadofprint

Résumé

Peripheral T-cell lymphomas (PTCLs) have a poor prognosis and, to date, there are no reliable predictive biomarkers of response. In this work we explored the prognostic impact of cell-free DNA (cfDNA) concentration in 75 newly diagnosed patients enrolled in a prospective multicenter study. Pre-treatment cfDNA was strongly associated with clinical risk factors and was identified as a superior predictor for shorter progression-free survival in multivariable analysis, outweighing canonical risk parameters. Furthermore, we identified a cfDNA value above which survival worsens. In conclusion, pre-treatment cfDNA concentration represents an easily usable predictive biomarker that is highly associated with survival of PTCL patients.

Identifiants

pubmed: 38176400
doi: 10.1111/bjh.19280
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Associazione Italiana per la Ricerca sul Cancro
ID : IG22089
Organisme : Associazione Italiana Contro le Leucemie - Linfomi e Mieloma

Informations de copyright

© 2024 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

Références

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Auteurs

E Fardella (E)

University of Milan, Milan, Italy.

G Zanirato (G)

Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

M Magni (M)

Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

N Caldarelli (N)

University of Milan, Milan, Italy.

A Chiappella (A)

Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

A Dodero (A)

Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

S Ljevar (S)

Unit of Biostatistics for Clinical Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

L Orsucci (L)

Division of Hematology, Azienda Ospedaliera e Universitaria Città della Salute e della Scienza, Turin, Italy.

A Re (A)

Hematology Division, ASST Spedali Civili di Brescia, Brescia, Italy.

S V Usai (SV)

Hematology Unit, Ospedale Oncologico Armando Businco, Cagliari, Italy.

V Stefoni (V)

Institute of Hematology Seràgnoli, University of Bologna, Bologna, Italy.

C Castellino (C)

Division of Hematology, Azienda Ospedaliera S. Croce e Carle, Cuneo, Italy.

F G Rossi (FG)

Division of Hematology, Fondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.

A Pinto (A)

Hematology-Oncology & Stem Cell Transplantation Unit, IRCCS Istituto Nazionale Tumori, Fondazione G. Pascale, Napoli, Italy.

C Carniti (C)

Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

P Corradini (P)

University of Milan, Milan, Italy.
Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Classifications MeSH