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Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy

BACKGROUND: Advanced breast cancer (ABC) is characterized by multidimensional clinical complexity that is usually not considered in randomized clinical trials. In the present real-life study, we investigated the link between clinical complexity and quality of life of patients with HR(+)/HER2(−) ABC...

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Autores principales: Tagliaferri, Barbara, Mollica, Ludovica, Palumbo, Raffella, Leli, Claudia, Malovini, Alberto, Terzaghi, Matteo, Quaquarini, Erica, Teragni, Cristina, Maccarone, Stefano, Premoli, Andrea, Sottotetti, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291968/
https://www.ncbi.nlm.nih.gov/pubmed/37378079
http://dx.doi.org/10.7573/dic.2023-1-7
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author Tagliaferri, Barbara
Mollica, Ludovica
Palumbo, Raffella
Leli, Claudia
Malovini, Alberto
Terzaghi, Matteo
Quaquarini, Erica
Teragni, Cristina
Maccarone, Stefano
Premoli, Andrea
Sottotetti, Federico
author_facet Tagliaferri, Barbara
Mollica, Ludovica
Palumbo, Raffella
Leli, Claudia
Malovini, Alberto
Terzaghi, Matteo
Quaquarini, Erica
Teragni, Cristina
Maccarone, Stefano
Premoli, Andrea
Sottotetti, Federico
author_sort Tagliaferri, Barbara
collection PubMed
description BACKGROUND: Advanced breast cancer (ABC) is characterized by multidimensional clinical complexity that is usually not considered in randomized clinical trials. In the present real-life study, we investigated the link between clinical complexity and quality of life of patients with HR(+)/HER2(−) ABC treated with CDK4/6 inhibitors. METHODS: We evaluated multimorbidity burden assessed with the Cumulative Illness Rating Scale (CIRS), polypharmacy and patient-reported outcomes (PROs). PROs were assessed at baseline (T0), after 3 months of therapy (T1), and at disease progression (T2) using EORTC QLC-C30 and QLQ-BR23 questionnaires. Baseline PROs and changes between T0 and T1 were evaluated amongst patients with different multimorbidity burden (CIRS <5 and ≥5) and polypharmacy (<2 or ≥2 drugs). RESULTS: From January 2018 to January 2022, we enrolled 54 patients (median age 66 years, IQR 59–74). The median CIRS score was 5 (IQR 2–7), whilst the median number of drugs taken by patients was 2 (IQR 0–4). No changes in QLQ-C30 final scoring between T0 and T1 were observed in the overall cohort (p=0.8944). At T2, QLQ-C30 global score deteriorated with respect to baseline (p=0.0089). At baseline, patients with CIRS ≥5 had worse constipation than patients without comorbidities (p<0.05) and a lower trend in the median QLQ-C30 global score. Patients on ≥2 drugs had lower QLQ-C30 final scores and worse insomnia and constipation (p<0.05). No change in QLQ-C30 final score from T0 to T1 was observed (p>0.05). CONCLUSION: Multimorbidity and polypharmacy increase the clinical complexity of patients with ABC and may affect baseline PROs. The safety profile of CDK4/6 inhibitors seems to be maintained in this population. Further studies are needed to assess clinical complexity in patients with ABC. This article is part of the Tackling clinical complexity in breast cancer Special Issue: https://www.drugsincontext.com/special_issues/tackling-clinical-complexity-in-breast-cancer/
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spelling pubmed-102919682023-06-27 Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy Tagliaferri, Barbara Mollica, Ludovica Palumbo, Raffella Leli, Claudia Malovini, Alberto Terzaghi, Matteo Quaquarini, Erica Teragni, Cristina Maccarone, Stefano Premoli, Andrea Sottotetti, Federico Drugs Context Original Research BACKGROUND: Advanced breast cancer (ABC) is characterized by multidimensional clinical complexity that is usually not considered in randomized clinical trials. In the present real-life study, we investigated the link between clinical complexity and quality of life of patients with HR(+)/HER2(−) ABC treated with CDK4/6 inhibitors. METHODS: We evaluated multimorbidity burden assessed with the Cumulative Illness Rating Scale (CIRS), polypharmacy and patient-reported outcomes (PROs). PROs were assessed at baseline (T0), after 3 months of therapy (T1), and at disease progression (T2) using EORTC QLC-C30 and QLQ-BR23 questionnaires. Baseline PROs and changes between T0 and T1 were evaluated amongst patients with different multimorbidity burden (CIRS <5 and ≥5) and polypharmacy (<2 or ≥2 drugs). RESULTS: From January 2018 to January 2022, we enrolled 54 patients (median age 66 years, IQR 59–74). The median CIRS score was 5 (IQR 2–7), whilst the median number of drugs taken by patients was 2 (IQR 0–4). No changes in QLQ-C30 final scoring between T0 and T1 were observed in the overall cohort (p=0.8944). At T2, QLQ-C30 global score deteriorated with respect to baseline (p=0.0089). At baseline, patients with CIRS ≥5 had worse constipation than patients without comorbidities (p<0.05) and a lower trend in the median QLQ-C30 global score. Patients on ≥2 drugs had lower QLQ-C30 final scores and worse insomnia and constipation (p<0.05). No change in QLQ-C30 final score from T0 to T1 was observed (p>0.05). CONCLUSION: Multimorbidity and polypharmacy increase the clinical complexity of patients with ABC and may affect baseline PROs. The safety profile of CDK4/6 inhibitors seems to be maintained in this population. Further studies are needed to assess clinical complexity in patients with ABC. This article is part of the Tackling clinical complexity in breast cancer Special Issue: https://www.drugsincontext.com/special_issues/tackling-clinical-complexity-in-breast-cancer/ BioExcel Publishing Ltd 2023-06-20 /pmc/articles/PMC10291968/ /pubmed/37378079 http://dx.doi.org/10.7573/dic.2023-1-7 Text en Copyright © 2023 Tagliaferri B, Mollica L, Palumbo R, Leli C, Malovini A, Terzaghi M, Quaquarini E, Teragni C, Maccarone S, Premoli A, Sottotetti F https://creativecommons.org/licenses/by-nc-nd/4.0/Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0, which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission.
spellingShingle Original Research
Tagliaferri, Barbara
Mollica, Ludovica
Palumbo, Raffella
Leli, Claudia
Malovini, Alberto
Terzaghi, Matteo
Quaquarini, Erica
Teragni, Cristina
Maccarone, Stefano
Premoli, Andrea
Sottotetti, Federico
Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy
title Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy
title_full Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy
title_fullStr Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy
title_full_unstemmed Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy
title_short Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR(+)/HER2(−) breast cancer treated with CDK4/6 inhibitors and endocrine therapy
title_sort health-related quality of life and clinical complexity of a real-life cohort of patients with advanced hr(+)/her2(−) breast cancer treated with cdk4/6 inhibitors and endocrine therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291968/
https://www.ncbi.nlm.nih.gov/pubmed/37378079
http://dx.doi.org/10.7573/dic.2023-1-7
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