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Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada

BACKGROUND: Little is known on the impact of emerging treatments for advanced melanoma (stages III and IV) on patients’ functioning and well-being. The objective of this study was to describe the patient-reported treatment-related symptom (TRS) burden in advanced melanoma. METHOD: Twenty-nine in-dep...

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Autores principales: Cheung, Winson Y., White, Michelle K., Bayliss, Martha S., Stroupe, Angela, Lovley, Andrew, King-Kallimanis, Bellinda L., Lasch, Kathryn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281076/
https://www.ncbi.nlm.nih.gov/pubmed/29934684
http://dx.doi.org/10.1007/s00520-018-4316-9
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author Cheung, Winson Y.
White, Michelle K.
Bayliss, Martha S.
Stroupe, Angela
Lovley, Andrew
King-Kallimanis, Bellinda L.
Lasch, Kathryn
author_facet Cheung, Winson Y.
White, Michelle K.
Bayliss, Martha S.
Stroupe, Angela
Lovley, Andrew
King-Kallimanis, Bellinda L.
Lasch, Kathryn
author_sort Cheung, Winson Y.
collection PubMed
description BACKGROUND: Little is known on the impact of emerging treatments for advanced melanoma (stages III and IV) on patients’ functioning and well-being. The objective of this study was to describe the patient-reported treatment-related symptom (TRS) burden in advanced melanoma. METHOD: Twenty-nine in-depth, qualitative interviews were conducted among adult patients with advanced melanoma in Canada using a semi-structured interview method. Interviews were transcribed verbatim, and key concepts were identified using a grounded theory analytic approach. RESULTS: The 29 patients reported 13 unique treatment journeys involving the following drug therapy categories: cytotoxic chemotherapies, CTLA-4 inhibitors, BRAF or MEK inhibitors, and PD-1 inhibitors. Patients typically underwent multiple treatment episodes over time. Common TRSs included nausea, fatigue, diarrhea or constipation, and skin rashes. Patients described these as impacting their physical functioning, ability to perform activities of daily living, social functioning, and overall quality of life. CONCLUSION: Our findings provide a description of the patient’s experience with treatment for advanced melanoma. Our sample included patients typically diagnosed in mid-life, facing an urgent sequence of medical procedures and a pharmacological treatment journey that was burdensome. There is a need for less toxic and more efficacious treatments earlier in the patient journey to alleviate the impact of advanced melanoma treatment on patients’ health-related quality of life.
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spelling pubmed-62810762018-12-26 Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada Cheung, Winson Y. White, Michelle K. Bayliss, Martha S. Stroupe, Angela Lovley, Andrew King-Kallimanis, Bellinda L. Lasch, Kathryn Support Care Cancer Original Article BACKGROUND: Little is known on the impact of emerging treatments for advanced melanoma (stages III and IV) on patients’ functioning and well-being. The objective of this study was to describe the patient-reported treatment-related symptom (TRS) burden in advanced melanoma. METHOD: Twenty-nine in-depth, qualitative interviews were conducted among adult patients with advanced melanoma in Canada using a semi-structured interview method. Interviews were transcribed verbatim, and key concepts were identified using a grounded theory analytic approach. RESULTS: The 29 patients reported 13 unique treatment journeys involving the following drug therapy categories: cytotoxic chemotherapies, CTLA-4 inhibitors, BRAF or MEK inhibitors, and PD-1 inhibitors. Patients typically underwent multiple treatment episodes over time. Common TRSs included nausea, fatigue, diarrhea or constipation, and skin rashes. Patients described these as impacting their physical functioning, ability to perform activities of daily living, social functioning, and overall quality of life. CONCLUSION: Our findings provide a description of the patient’s experience with treatment for advanced melanoma. Our sample included patients typically diagnosed in mid-life, facing an urgent sequence of medical procedures and a pharmacological treatment journey that was burdensome. There is a need for less toxic and more efficacious treatments earlier in the patient journey to alleviate the impact of advanced melanoma treatment on patients’ health-related quality of life. Springer Berlin Heidelberg 2018-06-23 2019 /pmc/articles/PMC6281076/ /pubmed/29934684 http://dx.doi.org/10.1007/s00520-018-4316-9 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Cheung, Winson Y.
White, Michelle K.
Bayliss, Martha S.
Stroupe, Angela
Lovley, Andrew
King-Kallimanis, Bellinda L.
Lasch, Kathryn
Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
title Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
title_full Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
title_fullStr Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
title_full_unstemmed Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
title_short Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
title_sort patient-reported treatment-related symptom burden for patients with advanced melanoma in canada
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281076/
https://www.ncbi.nlm.nih.gov/pubmed/29934684
http://dx.doi.org/10.1007/s00520-018-4316-9
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