Cargando…
Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer
PURPOSE: To prospectively compare HRQoL effects of two modern adjuvant chemotherapy breast cancer treatment regimens at six time-points up to 16 months after random assignment. METHODS: The open-label, randomized, Phase 3 “Panther trial” was conducted between February 2007 and September 2011. 760 wo...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182635/ https://www.ncbi.nlm.nih.gov/pubmed/32232698 http://dx.doi.org/10.1007/s10549-020-05602-9 |
_version_ | 1783526269259874304 |
---|---|
author | Brandberg, Yvonne Johansson, Hemming Hellström, Mats Gnant, Michael Möbus, Volker Greil, Richard Foukakis, Theodoros Bergh, Jonas |
author_facet | Brandberg, Yvonne Johansson, Hemming Hellström, Mats Gnant, Michael Möbus, Volker Greil, Richard Foukakis, Theodoros Bergh, Jonas |
author_sort | Brandberg, Yvonne |
collection | PubMed |
description | PURPOSE: To prospectively compare HRQoL effects of two modern adjuvant chemotherapy breast cancer treatment regimens at six time-points up to 16 months after random assignment. METHODS: The open-label, randomized, Phase 3 “Panther trial” was conducted between February 2007 and September 2011. 760 women, aged 65 years and younger, after surgery for non-metastatic node-positive or high-risk node-negative breast cancer were randomized 1:1 to the experimental group (four cycles of tailored and dose-dense adjuvant epirubicin and cyclophosphamide/2 weeks followed by four cycles of tailored dose-dense docetaxel/2 weeks) or standard group (three cycles of fluorouracil and epirubicin-cyclophosphamide/3 weeks followed by three cycles of docetaxel/3 weeks). HRQoL was assessed at all Swedish centres using EORTC QLQ-C30 and EORTC QLQ-BR23 at six points during 16 months before randomization. RESULTS: Response rates to questionnaires were highest at baseline 728/780 (93%) and lowest 16 months after randomization, 557/750 (74%). HRQoL declined during treatment in both groups. At the end of treatment, the experimental group reported statistically significantly lower HRQoL (P < 0.001) than the standard group on global health status, physical functioning, role functioning, social functioning, fatigue, sexual functioning, and systemic therapy effects. No differences were found for emotional functioning, body image, and arm and breast symptoms. There were no statistically significant differences between the groups at the first follow-up and at subsequent assessments. HRQoL levels at the 16-month follow-up were similar to baseline values. CONCLUSIONS: Negative HRQoL impact of the dose-dense and tailored strategy appears to be prominent during treatment, but HRQoL recover once treatment ends. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00798070; isrctn.org Identifier: ISRCTN39017665. |
format | Online Article Text |
id | pubmed-7182635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-71826352020-04-29 Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer Brandberg, Yvonne Johansson, Hemming Hellström, Mats Gnant, Michael Möbus, Volker Greil, Richard Foukakis, Theodoros Bergh, Jonas Breast Cancer Res Treat Clinical Trial PURPOSE: To prospectively compare HRQoL effects of two modern adjuvant chemotherapy breast cancer treatment regimens at six time-points up to 16 months after random assignment. METHODS: The open-label, randomized, Phase 3 “Panther trial” was conducted between February 2007 and September 2011. 760 women, aged 65 years and younger, after surgery for non-metastatic node-positive or high-risk node-negative breast cancer were randomized 1:1 to the experimental group (four cycles of tailored and dose-dense adjuvant epirubicin and cyclophosphamide/2 weeks followed by four cycles of tailored dose-dense docetaxel/2 weeks) or standard group (three cycles of fluorouracil and epirubicin-cyclophosphamide/3 weeks followed by three cycles of docetaxel/3 weeks). HRQoL was assessed at all Swedish centres using EORTC QLQ-C30 and EORTC QLQ-BR23 at six points during 16 months before randomization. RESULTS: Response rates to questionnaires were highest at baseline 728/780 (93%) and lowest 16 months after randomization, 557/750 (74%). HRQoL declined during treatment in both groups. At the end of treatment, the experimental group reported statistically significantly lower HRQoL (P < 0.001) than the standard group on global health status, physical functioning, role functioning, social functioning, fatigue, sexual functioning, and systemic therapy effects. No differences were found for emotional functioning, body image, and arm and breast symptoms. There were no statistically significant differences between the groups at the first follow-up and at subsequent assessments. HRQoL levels at the 16-month follow-up were similar to baseline values. CONCLUSIONS: Negative HRQoL impact of the dose-dense and tailored strategy appears to be prominent during treatment, but HRQoL recover once treatment ends. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT00798070; isrctn.org Identifier: ISRCTN39017665. Springer US 2020-03-31 2020 /pmc/articles/PMC7182635/ /pubmed/32232698 http://dx.doi.org/10.1007/s10549-020-05602-9 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/. |
spellingShingle | Clinical Trial Brandberg, Yvonne Johansson, Hemming Hellström, Mats Gnant, Michael Möbus, Volker Greil, Richard Foukakis, Theodoros Bergh, Jonas Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
title | Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
title_full | Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
title_fullStr | Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
title_full_unstemmed | Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
title_short | Long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
title_sort | long-term (up to 16 months) health-related quality of life after adjuvant tailored dose-dense chemotherapy vs. standard three-weekly chemotherapy in women with high-risk early breast cancer |
topic | Clinical Trial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7182635/ https://www.ncbi.nlm.nih.gov/pubmed/32232698 http://dx.doi.org/10.1007/s10549-020-05602-9 |
work_keys_str_mv | AT brandbergyvonne longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT johanssonhemming longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT hellstrommats longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT gnantmichael longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT mobusvolker longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT greilrichard longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT foukakistheodoros longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT berghjonas longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer AT longtermupto16monthshealthrelatedqualityoflifeafteradjuvanttailoreddosedensechemotherapyvsstandardthreeweeklychemotherapyinwomenwithhighriskearlybreastcancer |