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Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer

OBJECTIVES: Few studies to date have investigated the prognostic significance of Ki67 expression as a continuous variable in breast cancer. This study aimed to evaluate the impact of Ki67 expression as a dichotomous or continuous variable on outcomes in estrogen receptor (ER)+ and human epidermal gr...

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Autores principales: Ushimado, Kaori, Kobayashi, Naomi, Hikichi, Masahiro, Tsukamoto, Tetsuya, Urano, Makoto, Utsumi, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fujita Medical Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766244/
https://www.ncbi.nlm.nih.gov/pubmed/35111506
http://dx.doi.org/10.20407/fmj.2018-021
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author Ushimado, Kaori
Kobayashi, Naomi
Hikichi, Masahiro
Tsukamoto, Tetsuya
Urano, Makoto
Utsumi, Toshiaki
author_facet Ushimado, Kaori
Kobayashi, Naomi
Hikichi, Masahiro
Tsukamoto, Tetsuya
Urano, Makoto
Utsumi, Toshiaki
author_sort Ushimado, Kaori
collection PubMed
description OBJECTIVES: Few studies to date have investigated the prognostic significance of Ki67 expression as a continuous variable in breast cancer. This study aimed to evaluate the impact of Ki67 expression as a dichotomous or continuous variable on outcomes in estrogen receptor (ER)+ and human epidermal growth factor receptor 2 (HER2)– breast cancer. METHODS: Survival analysis was performed to estimate the likelihood of distant recurrence and death in retrospective data from 794 patients with ER+/HER2– breast cancer. We assessed the relationship between outcomes and two Ki67 cutoffs, 14% and 20%, and the Ki67 labeling index as a continuous variable. RESULTS: In univariate analysis, T stage, lymph node involvement, histological grade, progesterone receptor status, and Ki67 expression at the two cutoffs and as a continuous variable were identified as significant prognostic factors for distant disease-free survival (DDFS) and overall survival (OS). There were no statistical differences in DDFS and OS between women with Ki67 expression of <14% and 14–<20%. Multivariate analysis showed that Ki67 expression ≥20% was an independent prognostic indicator for DDFS. Regarding the risk of distant metastasis, the 20% cutoff was more reliable than 14%. We also found that Ki67 expression as a continuous variable was an independent prognostic factor for DDFS and OS in multivariate analyses. CONCLUSIONS: High Ki67 expression is associated with a survival disadvantage in patients with ER+/HER2– breast cancer, indicating that these patients might have a higher risk of recurrence after primary treatment and might therefore benefit from individualized treatment.
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spelling pubmed-87662442022-02-01 Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer Ushimado, Kaori Kobayashi, Naomi Hikichi, Masahiro Tsukamoto, Tetsuya Urano, Makoto Utsumi, Toshiaki Fujita Med J Original Article OBJECTIVES: Few studies to date have investigated the prognostic significance of Ki67 expression as a continuous variable in breast cancer. This study aimed to evaluate the impact of Ki67 expression as a dichotomous or continuous variable on outcomes in estrogen receptor (ER)+ and human epidermal growth factor receptor 2 (HER2)– breast cancer. METHODS: Survival analysis was performed to estimate the likelihood of distant recurrence and death in retrospective data from 794 patients with ER+/HER2– breast cancer. We assessed the relationship between outcomes and two Ki67 cutoffs, 14% and 20%, and the Ki67 labeling index as a continuous variable. RESULTS: In univariate analysis, T stage, lymph node involvement, histological grade, progesterone receptor status, and Ki67 expression at the two cutoffs and as a continuous variable were identified as significant prognostic factors for distant disease-free survival (DDFS) and overall survival (OS). There were no statistical differences in DDFS and OS between women with Ki67 expression of <14% and 14–<20%. Multivariate analysis showed that Ki67 expression ≥20% was an independent prognostic indicator for DDFS. Regarding the risk of distant metastasis, the 20% cutoff was more reliable than 14%. We also found that Ki67 expression as a continuous variable was an independent prognostic factor for DDFS and OS in multivariate analyses. CONCLUSIONS: High Ki67 expression is associated with a survival disadvantage in patients with ER+/HER2– breast cancer, indicating that these patients might have a higher risk of recurrence after primary treatment and might therefore benefit from individualized treatment. Fujita Medical Society 2019 2019-04-17 /pmc/articles/PMC8766244/ /pubmed/35111506 http://dx.doi.org/10.20407/fmj.2018-021 Text en https://creativecommons.org/licenses/by/4.0/This is an Open access article distributed under the Terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Ushimado, Kaori
Kobayashi, Naomi
Hikichi, Masahiro
Tsukamoto, Tetsuya
Urano, Makoto
Utsumi, Toshiaki
Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer
title Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer
title_full Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer
title_fullStr Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer
title_full_unstemmed Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer
title_short Inverse correlation between Ki67 expression as a continuous variable and outcomes in luminal HER2-negative breast cancer
title_sort inverse correlation between ki67 expression as a continuous variable and outcomes in luminal her2-negative breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766244/
https://www.ncbi.nlm.nih.gov/pubmed/35111506
http://dx.doi.org/10.20407/fmj.2018-021
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