Value of combining biological age with assessment of individual frailty to optimize management of cancer treated with targeted therapies: model of chronic myeloid leukemia treated with tyrosine kinase inhibitors (BIO-TIMER trial).


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
30 May 2024
Historique:
received: 26 04 2024
accepted: 22 05 2024
medline: 31 5 2024
pubmed: 31 5 2024
entrez: 30 5 2024
Statut: epublish

Résumé

In the era of targeted therapies, the influence of aging on cancer management varies from one patient to another. Assessing individual frailty using geriatric tools has its limitations, and is not appropriate for all patients especially the youngest one. Thus, assessing the complementary value of a potential biomarker of individual aging is a promising field of investigation. The chronic myeloid leukemia model allows us to address this question with obvious advantages: longest experience in the use of tyrosine kinase inhibitors, standardization of therapeutic management and response with minimal residual disease and no effect on age-related diseases. Therefore, the aim of the BIO-TIMER study is to assess the biological age of chronic myeloid leukemia or non-malignant cells in patients treated with tyrosine kinase inhibitors and to determine its relevance, in association or not with individual frailty to optimize the personalised management of each patient. The BIO-TIMER study is a multi-center, prospective, longitudinal study aiming to evaluate the value of combining biological age determination by DNA methylation profile with individual frailty assessment to personalize the management of chronic myeloid leukemia patients treated with tyrosine kinase inhibitors. Blood samples will be collected at diagnosis, 3 months and 12 months after treatment initiation. Individual frailty and quality of life will be assess at diagnosis, 6 months after treatment initiation, and then annually for 3 years. Tolerance to tyrosine kinase inhibitors will also be assessed during the 3-year follow-up. The study plans to recruit 321 patients and recruitment started in November 2023. The assessment of individual frailty should make it possible to personalize the treatment and care of patients. The BIO-TIMER study will provide new data on the role of aging in the management of chronic myeloid leukemia patients treated with tyrosine kinase inhibitors, which could influence clinical decision-making. ClinicalTrials.gov , ID NCT06130787; registered on November 14, 2023.

Sections du résumé

BACKGROUND BACKGROUND
In the era of targeted therapies, the influence of aging on cancer management varies from one patient to another. Assessing individual frailty using geriatric tools has its limitations, and is not appropriate for all patients especially the youngest one. Thus, assessing the complementary value of a potential biomarker of individual aging is a promising field of investigation. The chronic myeloid leukemia model allows us to address this question with obvious advantages: longest experience in the use of tyrosine kinase inhibitors, standardization of therapeutic management and response with minimal residual disease and no effect on age-related diseases. Therefore, the aim of the BIO-TIMER study is to assess the biological age of chronic myeloid leukemia or non-malignant cells in patients treated with tyrosine kinase inhibitors and to determine its relevance, in association or not with individual frailty to optimize the personalised management of each patient.
METHODS METHODS
The BIO-TIMER study is a multi-center, prospective, longitudinal study aiming to evaluate the value of combining biological age determination by DNA methylation profile with individual frailty assessment to personalize the management of chronic myeloid leukemia patients treated with tyrosine kinase inhibitors. Blood samples will be collected at diagnosis, 3 months and 12 months after treatment initiation. Individual frailty and quality of life will be assess at diagnosis, 6 months after treatment initiation, and then annually for 3 years. Tolerance to tyrosine kinase inhibitors will also be assessed during the 3-year follow-up. The study plans to recruit 321 patients and recruitment started in November 2023.
DISCUSSION CONCLUSIONS
The assessment of individual frailty should make it possible to personalize the treatment and care of patients. The BIO-TIMER study will provide new data on the role of aging in the management of chronic myeloid leukemia patients treated with tyrosine kinase inhibitors, which could influence clinical decision-making.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov , ID NCT06130787; registered on November 14, 2023.

Identifiants

pubmed: 38816821
doi: 10.1186/s12885-024-12415-2
pii: 10.1186/s12885-024-12415-2
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Tyrosine Kinase Inhibitors 0

Banques de données

ClinicalTrials.gov
['NCT06130787']

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

661

Subventions

Organisme : Fondation ARC pour la Recherche sur le Cancer
ID : ARCAGEING2022040004945

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Mélanie Casile (M)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France. mcasile@chu-clermontferrand.fr.
EA 7453 CHELTER, University of Clermont Auvergne, Clermont-Ferrand, France. mcasile@chu-clermontferrand.fr.

Gilles Albrand (G)

Geriatric Evaluation and Management unit, Antoine Charial Hospital, Francheville, Lyon, France.

Benjamin Lebecque (B)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
EA 7453 CHELTER, University of Clermont Auvergne, Clermont-Ferrand, France.

Joévin Besombes (J)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
EA 7453 CHELTER, University of Clermont Auvergne, Clermont-Ferrand, France.

Céline Bourgne (C)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
EA 7453 CHELTER, University of Clermont Auvergne, Clermont-Ferrand, France.

Bruno Pereira (B)

Biostatistics Unit, Clinical Research and Innovation Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Sandrine Saugues (S)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Biological Resources Centre - Auvergne, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Caroline Jamot (C)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Biological Resources Centre - Auvergne, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Eric Hermet (E)

Clinical Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Marc G Berger (MG)

Biological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
EA 7453 CHELTER, University of Clermont Auvergne, Clermont-Ferrand, France.
Biological Resources Centre - Auvergne, CHU Clermont-Ferrand, Clermont-Ferrand, France.

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