A new cytokine-based dynamic stratification during induction is highly predictive of survivals in acute myeloid leukemia.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
01 2021
Historique:
received: 17 04 2020
revised: 29 10 2020
accepted: 19 11 2020
pubmed: 29 12 2020
medline: 20 7 2021
entrez: 28 12 2020
Statut: ppublish

Résumé

The aim of this study was to assess the potential impact of the kinetics of serum levels of seven cytokines during induction in acute myeloid leukemia (AML) patients. Indeed, the role of cytokines, in the pathophysiology and response to therapy of AML patients, remains under investigation. Here, we report on the impact of peripheral levels of two cytokines, the Fms-like tyrosine kinase 3 ligand (FL) and interleukin-6 (IL-6), evaluated during first-line intensive induction. A new risk stratification can be proposed, which supersedes the ELN 2017 classification to predict survivals in AML patients by examining the kinetic profile of these cytokines during the induction phase. It segregates three groups of, respectively, high-risk, characterized by a stagnation of low FL levels, intermediate risk, with dynamic increasing FL levels and high IL-6 at day 22, and favorable risk with increasing FL levels but low IL-6 at day 22.

Identifiants

pubmed: 33369136
doi: 10.1002/cam4.3648
pmc: PMC7877358
doi:

Substances chimiques

Biomarkers, Tumor 0
IL6 protein, human 0
Interleukin-6 0
Membrane Proteins 0
flt3 ligand protein 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

642-648

Informations de copyright

© 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Pierre Peterlin (P)

Hematology Clinic, CHU, Nantes, France.
CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

Joelle Gaschet (J)

CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

Thierry Guillaume (T)

Hematology Clinic, CHU, Nantes, France.
CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

Alice Garnier (A)

Hematology Clinic, CHU, Nantes, France.

Marion Eveillard (M)

CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.
Hematology Biology, CHU, Nantes, France.

Amandine Le Bourgeois (A)

Hematology Clinic, CHU, Nantes, France.

Michel Cherel (M)

CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.
Nuclear Medicine Unit, ICO Cancer Center Gauducheau, Saint Herblain, France.

Camille Debord (C)

Hematology Biology, CHU, Nantes, France.

Yannick Le Bris (Y)

CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.
Hematology Biology, CHU, Nantes, France.

Olivier Theisen (O)

Hematology Biology, CHU, Nantes, France.

Catherine Godon (C)

Hematology Biology, CHU, Nantes, France.

Béatrice Mahé (B)

Hematology Clinic, CHU, Nantes, France.

Viviane Dubruille (V)

Hematology Clinic, CHU, Nantes, France.

Soraya Wuilleme (S)

Hematology Biology, CHU, Nantes, France.

Cyrille Touzeau (C)

Hematology Clinic, CHU, Nantes, France.

Thomas Gastinne (T)

Hematology Clinic, CHU, Nantes, France.

Nicolas Blin (N)

Hematology Clinic, CHU, Nantes, France.

Anne Lok (A)

Hematology Clinic, CHU, Nantes, France.

Benoît Tessoulin (B)

Hematology Clinic, CHU, Nantes, France.

Steven Le Gouill (S)

Hematology Clinic, CHU, Nantes, France.
CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

Philippe Moreau (P)

Hematology Clinic, CHU, Nantes, France.
CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

Marie-C Béné (MC)

CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.
Hematology Biology, CHU, Nantes, France.

Patrice Chevallier (P)

Hematology Clinic, CHU, Nantes, France.
CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

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