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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)
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...
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Published in: | BMC cancer 2024-05, Vol.24 (1), p.661-8, Article 661 |
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description | 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. |
doi_str_mv | 10.1186/s12885-024-12415-2 |
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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.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-024-12415-2</identifier><identifier>PMID: 38816821</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Age ; Age determination ; Aged ; Aged, 80 and over ; Aging ; Biological Age ; Biomarkers ; Bone marrow ; Cancer therapies ; Chronic myeloid leukemia ; Decision making ; Demographic aspects ; Diagnosis ; Disease management ; DNA Methylation ; Drug dosages ; Drug therapy ; Female ; Frailty ; Health aspects ; Humans ; Individual Frailty ; Influence ; ISO standards ; Leukemia ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy ; Longitudinal Studies ; Male ; Middle Aged ; Minimal residual disease ; Molecular Targeted Therapy ; Mortality ; Myeloid leukemia ; Observatories ; Patients ; Precision medicine ; Precision Medicine - methods ; Prospective Studies ; Protein Kinase Inhibitors - therapeutic use ; Quality of Life ; Standardization ; Tyrosine Kinase Inhibitors</subject><ispartof>BMC cancer, 2024-05, Vol.24 (1), p.661-8, Article 661</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-dac54bf98113dd4e0181840f9c1a3c1b89237ef84b3370c2b7bf7213e5e1f3053</citedby><cites>FETCH-LOGICAL-c503t-dac54bf98113dd4e0181840f9c1a3c1b89237ef84b3370c2b7bf7213e5e1f3053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/3066880994?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25751,27922,27923,37010,37011,44588</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38816821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Casile, Mélanie</creatorcontrib><creatorcontrib>Albrand, Gilles</creatorcontrib><creatorcontrib>Lebecque, Benjamin</creatorcontrib><creatorcontrib>Besombes, Joévin</creatorcontrib><creatorcontrib>Bourgne, Céline</creatorcontrib><creatorcontrib>Pereira, Bruno</creatorcontrib><creatorcontrib>Saugues, Sandrine</creatorcontrib><creatorcontrib>Jamot, Caroline</creatorcontrib><creatorcontrib>Hermet, Eric</creatorcontrib><creatorcontrib>Berger, Marc G</creatorcontrib><title>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)</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>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.</description><subject>Adult</subject><subject>Age</subject><subject>Age determination</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging</subject><subject>Biological Age</subject><subject>Biomarkers</subject><subject>Bone marrow</subject><subject>Cancer therapies</subject><subject>Chronic myeloid leukemia</subject><subject>Decision making</subject><subject>Demographic aspects</subject><subject>Diagnosis</subject><subject>Disease management</subject><subject>DNA Methylation</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Frailty</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Individual Frailty</subject><subject>Influence</subject><subject>ISO standards</subject><subject>Leukemia</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Minimal residual disease</subject><subject>Molecular Targeted Therapy</subject><subject>Mortality</subject><subject>Myeloid leukemia</subject><subject>Observatories</subject><subject>Patients</subject><subject>Precision medicine</subject><subject>Precision Medicine - methods</subject><subject>Prospective Studies</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Quality of Life</subject><subject>Standardization</subject><subject>Tyrosine Kinase Inhibitors</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptks1u1DAUhSMEoqXwAiyQJSTULlLsOJk47EpVYKSiSqWwtRznJnNbxx5sBxjel_fA02lLp0Je-EffObbvPVn2ktFDxsTsbWCFEFVOizJnRcmqvHiU7bKyZnlR0vrxvfVO9iyES0pZLah4mu1wIdhMFGw3-_NNmQmI64l2Y4sW7UBadMYNqJUhagDyE-OCqBAghBFsXLNoO_yB3ZSI3is0cUWiI24ZccTfQEZlk_AW1spq8CR6UBG6jV1UfoD1Li7AqyVCeEdG14G5Fiy8s6jJuALjsCMGpisYUT2wWHkX0AK5QqsCpDctsMXofCD77-dn-cX888l5kqAyB8-zJ70yAV7czHvZ1w8nF8ef8tOzj_Pjo9NcV5THvFO6Ktu-EYzxriuBMsFESftGM8U1a0VT8Bp6Ubac11QXbd32dcE4VMB6Tiu-l803vp1Tl3LpcVR-JZ1CeX3g_CCVj6gNyLahmvG-g4J2pQDeclrPWMPatkoX6D557W-8lt59nyBEOWLQYIyy4KYgOZ3xshJlQRP6-gF66SZv00_X1EwI2jTlP2pQ6X60vYte6bWpPKqbSswqUc8SdfgfKo0utUA7Cz2m8y3BwZYgMRF-xUFNIcj5l_Nt9s09dgHKxEVwZorobNgGiw2oU5ODh_6umIzKdfjlJvwyhV9eh18WSfTqpgxTO0J3J7lNO_8LGHQAyw</recordid><startdate>20240530</startdate><enddate>20240530</enddate><creator>Casile, Mélanie</creator><creator>Albrand, Gilles</creator><creator>Lebecque, Benjamin</creator><creator>Besombes, Joévin</creator><creator>Bourgne, Céline</creator><creator>Pereira, Bruno</creator><creator>Saugues, Sandrine</creator><creator>Jamot, Caroline</creator><creator>Hermet, Eric</creator><creator>Berger, Marc G</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20240530</creationdate><title>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)</title><author>Casile, Mélanie ; Albrand, Gilles ; Lebecque, Benjamin ; Besombes, Joévin ; Bourgne, Céline ; Pereira, Bruno ; Saugues, Sandrine ; Jamot, Caroline ; Hermet, Eric ; Berger, Marc G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-dac54bf98113dd4e0181840f9c1a3c1b89237ef84b3370c2b7bf7213e5e1f3053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Age</topic><topic>Age determination</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging</topic><topic>Biological Age</topic><topic>Biomarkers</topic><topic>Bone marrow</topic><topic>Cancer therapies</topic><topic>Chronic myeloid leukemia</topic><topic>Decision making</topic><topic>Demographic aspects</topic><topic>Diagnosis</topic><topic>Disease management</topic><topic>DNA Methylation</topic><topic>Drug dosages</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Frailty</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Individual Frailty</topic><topic>Influence</topic><topic>ISO standards</topic><topic>Leukemia</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Minimal residual disease</topic><topic>Molecular Targeted Therapy</topic><topic>Mortality</topic><topic>Myeloid leukemia</topic><topic>Observatories</topic><topic>Patients</topic><topic>Precision medicine</topic><topic>Precision Medicine - methods</topic><topic>Prospective Studies</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Quality of Life</topic><topic>Standardization</topic><topic>Tyrosine Kinase Inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Casile, Mélanie</creatorcontrib><creatorcontrib>Albrand, Gilles</creatorcontrib><creatorcontrib>Lebecque, Benjamin</creatorcontrib><creatorcontrib>Besombes, Joévin</creatorcontrib><creatorcontrib>Bourgne, Céline</creatorcontrib><creatorcontrib>Pereira, Bruno</creatorcontrib><creatorcontrib>Saugues, Sandrine</creatorcontrib><creatorcontrib>Jamot, Caroline</creatorcontrib><creatorcontrib>Hermet, Eric</creatorcontrib><creatorcontrib>Berger, Marc G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Casile, Mélanie</au><au>Albrand, Gilles</au><au>Lebecque, Benjamin</au><au>Besombes, Joévin</au><au>Bourgne, Céline</au><au>Pereira, Bruno</au><au>Saugues, Sandrine</au><au>Jamot, Caroline</au><au>Hermet, Eric</au><au>Berger, Marc G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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)</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2024-05-30</date><risdate>2024</risdate><volume>24</volume><issue>1</issue><spage>661</spage><epage>8</epage><pages>661-8</pages><artnum>661</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>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.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38816821</pmid><doi>10.1186/s12885-024-12415-2</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Age Age determination Aged Aged, 80 and over Aging Biological Age Biomarkers Bone marrow Cancer therapies Chronic myeloid leukemia Decision making Demographic aspects Diagnosis Disease management DNA Methylation Drug dosages Drug therapy Female Frailty Health aspects Humans Individual Frailty Influence ISO standards Leukemia Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy Longitudinal Studies Male Middle Aged Minimal residual disease Molecular Targeted Therapy Mortality Myeloid leukemia Observatories Patients Precision medicine Precision Medicine - methods Prospective Studies Protein Kinase Inhibitors - therapeutic use Quality of Life Standardization Tyrosine Kinase Inhibitors |
title | 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) |
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