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Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study

Clinical implications of frailty in myeloproliferative neoplasms (MPN), including essential thrombocythemia (ET), polycythemia vera (PV), and myelofibrosis (MF), are unknown. In this population-based study, all incident cases of MPN from the Ontario cancer registry between 2004 and 2019 (N = 10 336;...

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Autores principales: Bankar, Aniket, Chan, Wing C., Liu, Ning, Cheung, Matthew, Alibhai, Shabbir, Gupta, Vikas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471933/
https://www.ncbi.nlm.nih.gov/pubmed/37184988
http://dx.doi.org/10.1182/bloodadvances.2023009825
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author Bankar, Aniket
Chan, Wing C.
Liu, Ning
Cheung, Matthew
Alibhai, Shabbir
Gupta, Vikas
author_facet Bankar, Aniket
Chan, Wing C.
Liu, Ning
Cheung, Matthew
Alibhai, Shabbir
Gupta, Vikas
author_sort Bankar, Aniket
collection PubMed
description Clinical implications of frailty in myeloproliferative neoplasms (MPN), including essential thrombocythemia (ET), polycythemia vera (PV), and myelofibrosis (MF), are unknown. In this population-based study, all incident cases of MPN from the Ontario cancer registry between 2004 and 2019 (N = 10 336; ET = 5108; PV = 3843; MF = 1385) and their matched controls (for age, sex, residence, and income) in a 1:4 ratio were included. Baseline frailty measured using the Johns Hopkins Adjusted Clinical Groups frailty indicator and McIsaac frailty index (mFI), categorized as fit, prefrail, or frail if mFI <0.10, 0.11 to 0.20, >0.20), was significantly higher in ET, PV, and MF compared with matched controls (standardized mean difference of 0.27, 0.27, and 0.28). Over 23%, 20%, and 34% of patients with ET, PV, and MF were frail or prefrail despite a younger age (<65 years) or minimal comorbidities. In Cox proportional regression, frailty was independently associated with worse overall survival (OS) after adjusting for age, sex, and comorbidities compared with mFI-fit patients. The hazard ratios (95% confidence interval) for OS for mFI-prefrail and mFI-frail patients were: 1.6 (1.3-1.9) and 3.6 (2.9-4.4) in ET, 1.3 (1.1-1.5) and 2.7 (2.1-3.4) in PV, and 1.2 (1.0-1.5) and 2.0 (1.5-2.7) in MF. Patients with MPN have a substantially higher prevalence of frailty compared with matched controls, which is associated with reduced OS, independent of age or comorbidities.
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spelling pubmed-104719332023-09-02 Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study Bankar, Aniket Chan, Wing C. Liu, Ning Cheung, Matthew Alibhai, Shabbir Gupta, Vikas Blood Adv Health Services and Outcomes Clinical implications of frailty in myeloproliferative neoplasms (MPN), including essential thrombocythemia (ET), polycythemia vera (PV), and myelofibrosis (MF), are unknown. In this population-based study, all incident cases of MPN from the Ontario cancer registry between 2004 and 2019 (N = 10 336; ET = 5108; PV = 3843; MF = 1385) and their matched controls (for age, sex, residence, and income) in a 1:4 ratio were included. Baseline frailty measured using the Johns Hopkins Adjusted Clinical Groups frailty indicator and McIsaac frailty index (mFI), categorized as fit, prefrail, or frail if mFI <0.10, 0.11 to 0.20, >0.20), was significantly higher in ET, PV, and MF compared with matched controls (standardized mean difference of 0.27, 0.27, and 0.28). Over 23%, 20%, and 34% of patients with ET, PV, and MF were frail or prefrail despite a younger age (<65 years) or minimal comorbidities. In Cox proportional regression, frailty was independently associated with worse overall survival (OS) after adjusting for age, sex, and comorbidities compared with mFI-fit patients. The hazard ratios (95% confidence interval) for OS for mFI-prefrail and mFI-frail patients were: 1.6 (1.3-1.9) and 3.6 (2.9-4.4) in ET, 1.3 (1.1-1.5) and 2.7 (2.1-3.4) in PV, and 1.2 (1.0-1.5) and 2.0 (1.5-2.7) in MF. Patients with MPN have a substantially higher prevalence of frailty compared with matched controls, which is associated with reduced OS, independent of age or comorbidities. The American Society of Hematology 2023-05-26 /pmc/articles/PMC10471933/ /pubmed/37184988 http://dx.doi.org/10.1182/bloodadvances.2023009825 Text en © 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Health Services and Outcomes
Bankar, Aniket
Chan, Wing C.
Liu, Ning
Cheung, Matthew
Alibhai, Shabbir
Gupta, Vikas
Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
title Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
title_full Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
title_fullStr Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
title_full_unstemmed Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
title_short Prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
title_sort prevalence of frailty and its association with clinical outcomes in myeloproliferative neoplasms: a population-based study
topic Health Services and Outcomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471933/
https://www.ncbi.nlm.nih.gov/pubmed/37184988
http://dx.doi.org/10.1182/bloodadvances.2023009825
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