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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;...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society of Hematology
2023
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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. |
format | Online Article Text |
id | pubmed-10471933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society of Hematology |
record_format | MEDLINE/PubMed |
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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