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Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer
We assumed that the effect of adjuvant trastuzumab on survival is mediated by the treatment time and we conducted this trial-level meta-regression to determine the appropriate length of treatment. Twelve adjuvant trastuzumab trials (from January 2000 to June 2019, consisting of 20,271 patients) were...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406512/ https://www.ncbi.nlm.nih.gov/pubmed/32802960 http://dx.doi.org/10.1038/s41698-020-00128-1 |
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author | Yu, Ke-Da Wang, Xin Chen, Wan-Kun Fan, Lei Mo, Miao Chen, Han |
author_facet | Yu, Ke-Da Wang, Xin Chen, Wan-Kun Fan, Lei Mo, Miao Chen, Han |
author_sort | Yu, Ke-Da |
collection | PubMed |
description | We assumed that the effect of adjuvant trastuzumab on survival is mediated by the treatment time and we conducted this trial-level meta-regression to determine the appropriate length of treatment. Twelve adjuvant trastuzumab trials (from January 2000 to June 2019, consisting of 20,271 patients) were included. We considered 12-month trastuzumab treatment as the standard. The primary study endpoint was disease-free survival (DFS). By quantifying the relationship between shortened treatment time (month) and altered recurrence risk (expressed as hazard ratio), we found the regression coefficient β was 0.05 (95% confidence interval: 0.02–0.08, P = 0.002), indicating the recurrence risk would increase 5.1% for each month that treatment was shortened. Accordingly, 3, 6, and 9-month reductions in treatment time resulted in 16%, 35%, and 57% increases in recurrence risk, respectively. We revealed a significant linear association between shortened treatment time of trastuzumab and recurrence risk. The clinical duration of adjuvant trastuzumab should be tailored. |
format | Online Article Text |
id | pubmed-7406512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74065122020-08-13 Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer Yu, Ke-Da Wang, Xin Chen, Wan-Kun Fan, Lei Mo, Miao Chen, Han NPJ Precis Oncol Article We assumed that the effect of adjuvant trastuzumab on survival is mediated by the treatment time and we conducted this trial-level meta-regression to determine the appropriate length of treatment. Twelve adjuvant trastuzumab trials (from January 2000 to June 2019, consisting of 20,271 patients) were included. We considered 12-month trastuzumab treatment as the standard. The primary study endpoint was disease-free survival (DFS). By quantifying the relationship between shortened treatment time (month) and altered recurrence risk (expressed as hazard ratio), we found the regression coefficient β was 0.05 (95% confidence interval: 0.02–0.08, P = 0.002), indicating the recurrence risk would increase 5.1% for each month that treatment was shortened. Accordingly, 3, 6, and 9-month reductions in treatment time resulted in 16%, 35%, and 57% increases in recurrence risk, respectively. We revealed a significant linear association between shortened treatment time of trastuzumab and recurrence risk. The clinical duration of adjuvant trastuzumab should be tailored. Nature Publishing Group UK 2020-08-05 /pmc/articles/PMC7406512/ /pubmed/32802960 http://dx.doi.org/10.1038/s41698-020-00128-1 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yu, Ke-Da Wang, Xin Chen, Wan-Kun Fan, Lei Mo, Miao Chen, Han Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
title | Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
title_full | Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
title_fullStr | Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
title_full_unstemmed | Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
title_short | Tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
title_sort | tailored duration of adjuvant trastuzumab for human epidermal growth factor receptor 2-positive breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406512/ https://www.ncbi.nlm.nih.gov/pubmed/32802960 http://dx.doi.org/10.1038/s41698-020-00128-1 |
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