Evidence map›Paper›PMID 38816821›Full record

ArticleBMC cancer2024

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).

Mélanie Casile, Gilles Albrand, Clément Lahaye, Benjamin Lebecque, Joévin Besombes, Céline Bourgne, Bruno Pereira, Sandrine Saugues, Caroline Jamot, Eric Hermet and 1 more

Erratum issued Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT06130787 (Value of Biological Age, in Addition to Individual Frailty, for Personalising the Management of Cancer Treated with Targeted Therapy), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06130787 narecruitingnot on this map

Value of Biological Age, in Addition to Individual Frailty, for Personalising the Management of Cancer Treated with Targeted Therapy: the Model of Chronic Myeloid Leukemia Treated with Tyrosine Kinase Inhibitors.

TypeinterventionalSponsorUniversity Hospital, Clermont-FerrandRan2023 to 2028Enrolled321ConditionsLeukemia,Myeloid, ChronicArmsBlood and bone marrow sample
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Mélanie CasileBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France. mcasile@chu-clermontferrand.fr.
Gilles AlbrandGeriatric Evaluation and Management unit, Antoine Charial Hospital, Francheville, Lyon, France.
Clément LahayeUnité mobile de Gériatrie, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Benjamin LebecqueBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Joévin BesombesBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Céline BourgneBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Bruno PereiraBiostatistics Unit, Clinical Research and Innovation Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Sandrine SauguesBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Caroline JamotBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Eric HermetClinical Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Marc G BergerBiological Hematology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Funding

Fondation ARC pour la Recherche sur le Cancer ARCAGEING2022040004945
6 · The paper itself

Abstract

backgroundIn 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.

methodsThe 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: 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 registrationClinicalTrials.gov , ID NCT06130787; registered on November 14, 2023.

Indexed as

FrailtyLeukemia, Myelogenous, Chronic, BCR-ABL PositiveTyrosine Kinase InhibitorsAdultAgedAged, 80 and overAgingDNA MethylationFemaleHumansLongitudinal StudiesMaleMiddle AgedMolecular Targeted TherapyPrecision MedicineProspective StudiesTyrosine Kinase InhibitorsBiological AgeChronic myeloid leukemiaIndividual FrailtyTyrosine kinase inhibitors

Identifiers

PMID38816821
PMCPMC11140958

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.