Cargando…
Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial
BACKGROUND: Despite its proven efficacy in reducing recurrence and improving survival, adherence to endocrine therapy (ET) is suboptimal in women with breast cancer (BC). Health-related quality of life (HRQoL) in BC has been widely studied and many positive effects have been highlighted. Recently, a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296931/ https://www.ncbi.nlm.nih.gov/pubmed/32546198 http://dx.doi.org/10.1186/s13063-020-04397-w |
_version_ | 1783546925971144704 |
---|---|
author | Mamguem Kamga, Ariane Di Martino, Cyril Anota, Amelie Paget-Bailly, Sophie Coutant, Charles Arveux, Patrick Desmoulins, Isabelle Dabakuyo-Yonli, Tienhan Sandrine |
author_facet | Mamguem Kamga, Ariane Di Martino, Cyril Anota, Amelie Paget-Bailly, Sophie Coutant, Charles Arveux, Patrick Desmoulins, Isabelle Dabakuyo-Yonli, Tienhan Sandrine |
author_sort | Mamguem Kamga, Ariane |
collection | PubMed |
description | BACKGROUND: Despite its proven efficacy in reducing recurrence and improving survival, adherence to endocrine therapy (ET) is suboptimal in women with breast cancer (BC). Health-related quality of life (HRQoL) in BC has been widely studied and many positive effects have been highlighted. Recently, a link between HRQoL and compliance with ET has been suggested, which would suggest a potential role for HRQoL assessment in improving compliance with ET. With the advent of digital technologies, electronic collection of HRQoL on a tablet is now possible. Thus, we hypothesize that systematic HRQoL assessment (using a tablet, prior to each consultation, with presentation of scores to clinicians) coupled with therapeutic information could have an impact on 12-month compliance with ET in patients with non-metastatic BC. METHODS: In this study, we will include 342 women with non-metastatic hormone receptor–positive BC with an indication for treatment with ET. Patients will be randomly assigned 1:1 by minimization and stratified by age, stage, type of ET prescribed, and presence of comorbidities (or not) in two arms. The intervention will consist of numerical HRQoL assessment using the CHES (Computer-based Health Evaluation System) software before each consultation (with delivery of scores to clinicians) coupled with therapeutic information. Therapeutic information will consist of three workshops related to understanding the prescription, nutrition, and fatigue. A reminder letter will be sent to patients every month. Patients in the control group will follow standard care. HRQoL will be assessed using a classic “paper-pencil” collection at baseline in both arms to ensure comparability between arms and at 12 months. The primary endpoint is 12-month compliance with ET. Patient satisfaction with care and the clinicians’ perception of the usefulness of routine HRQoL assessment will also be assessed. DISCUSSION: This study will allow clinicians to identify and better understand the areas in which patients who receive ET have difficulties and thus it will assist clinicians with patient management. Systematic evaluation of HRQoL could provide an additional endpoint for measuring patients’ health status and treatment-related symptoms, including ET. If the results of this study are positive, this intervention could be proposed as an integral part of daily clinical practice in patients who receive ET. TRIAL REGISTRATION: ClinicalTrials.govNCT04176809. Registered Nov. 25, 2019. |
format | Online Article Text |
id | pubmed-7296931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72969312020-06-16 Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial Mamguem Kamga, Ariane Di Martino, Cyril Anota, Amelie Paget-Bailly, Sophie Coutant, Charles Arveux, Patrick Desmoulins, Isabelle Dabakuyo-Yonli, Tienhan Sandrine Trials Study Protocol BACKGROUND: Despite its proven efficacy in reducing recurrence and improving survival, adherence to endocrine therapy (ET) is suboptimal in women with breast cancer (BC). Health-related quality of life (HRQoL) in BC has been widely studied and many positive effects have been highlighted. Recently, a link between HRQoL and compliance with ET has been suggested, which would suggest a potential role for HRQoL assessment in improving compliance with ET. With the advent of digital technologies, electronic collection of HRQoL on a tablet is now possible. Thus, we hypothesize that systematic HRQoL assessment (using a tablet, prior to each consultation, with presentation of scores to clinicians) coupled with therapeutic information could have an impact on 12-month compliance with ET in patients with non-metastatic BC. METHODS: In this study, we will include 342 women with non-metastatic hormone receptor–positive BC with an indication for treatment with ET. Patients will be randomly assigned 1:1 by minimization and stratified by age, stage, type of ET prescribed, and presence of comorbidities (or not) in two arms. The intervention will consist of numerical HRQoL assessment using the CHES (Computer-based Health Evaluation System) software before each consultation (with delivery of scores to clinicians) coupled with therapeutic information. Therapeutic information will consist of three workshops related to understanding the prescription, nutrition, and fatigue. A reminder letter will be sent to patients every month. Patients in the control group will follow standard care. HRQoL will be assessed using a classic “paper-pencil” collection at baseline in both arms to ensure comparability between arms and at 12 months. The primary endpoint is 12-month compliance with ET. Patient satisfaction with care and the clinicians’ perception of the usefulness of routine HRQoL assessment will also be assessed. DISCUSSION: This study will allow clinicians to identify and better understand the areas in which patients who receive ET have difficulties and thus it will assist clinicians with patient management. Systematic evaluation of HRQoL could provide an additional endpoint for measuring patients’ health status and treatment-related symptoms, including ET. If the results of this study are positive, this intervention could be proposed as an integral part of daily clinical practice in patients who receive ET. TRIAL REGISTRATION: ClinicalTrials.govNCT04176809. Registered Nov. 25, 2019. BioMed Central 2020-06-16 /pmc/articles/PMC7296931/ /pubmed/32546198 http://dx.doi.org/10.1186/s13063-020-04397-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Mamguem Kamga, Ariane Di Martino, Cyril Anota, Amelie Paget-Bailly, Sophie Coutant, Charles Arveux, Patrick Desmoulins, Isabelle Dabakuyo-Yonli, Tienhan Sandrine Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
title | Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
title_full | Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
title_fullStr | Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
title_full_unstemmed | Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
title_short | Impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
title_sort | impact of routine assessment of health-related quality of life coupled with therapeutic information on compliance with endocrine therapy in patients with non-metastatic breast cancer: protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296931/ https://www.ncbi.nlm.nih.gov/pubmed/32546198 http://dx.doi.org/10.1186/s13063-020-04397-w |
work_keys_str_mv | AT mamguemkamgaariane impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT dimartinocyril impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT anotaamelie impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT pagetbaillysophie impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT coutantcharles impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT arveuxpatrick impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT desmoulinsisabelle impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial AT dabakuyoyonlitienhansandrine impactofroutineassessmentofhealthrelatedqualityoflifecoupledwiththerapeuticinformationoncompliancewithendocrinetherapyinpatientswithnonmetastaticbreastcancerprotocolforarandomizedcontrolledtrial |