TY - JOUR
T1 - Prognostic significance of the Ki67 scoring categories in breast cancer subgroups
AU - Niikura, Naoki
AU - Masuda, Shinobu
AU - Kumaki, Nobue
AU - Xiaoyan, Tang
AU - Terada, Mizuho
AU - Terao, Mayako
AU - Iwamoto, Takayuki
AU - Oshitanai, Risa
AU - Morioka, Toru
AU - Tuda, Banri
AU - Okamura, Takuho
AU - Saito, Yuki
AU - Suzuki, Yasuhiro
AU - Tokuda, Yutaka
N1 - Funding Information:
We thank Mitsuko Kobayashi for secretarial assistance. This research was supported in part by the MEXT-Supported Program for the Strategic Research Foundation at Private Universities, 2012-2016. The authors thank Editage for providing editorial assistance.
Publisher Copyright:
© 2014 Elsevier Inc.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2014
Y1 - 2014
N2 - We aimed to estimate the usefulness of scoring categories of IHC Ki67 as a prognostic factor for breast cancer subgroups. Our data demonstrated that Ki67 scores have a prognostic value in breast cancer patients with ERpositive and HER2-negative tumors. Background: Immunohistochemical (IHC) expression of Ki67 has a prognostic and predictive value for breast cancer, and the IHC Ki67 labeling index is estimated by counting the number of positive and negative cells. It has not been clarified whether IHC Ki67 estimated using a semiquantitative scoring system has a prognostic value. We aimed to estimate the usefulness of scoring categories of IHC Ki67 as a prognostic factor for breast cancer subgroups. Patients and Methods: We retrospectively identified patients in the Tokai University breast cancer database for whom IHC Ki67 data were available between January 1, 2000 and December 31, 2010. Survival curves were calculated using the Kaplan-Meier method and compared using the log-rank test. Results: Of the 1331 primary breast cancer patients included in the study, In patients with estrogen receptor (ER)-positive and HER2-negative tumors (n = 971), high and intermediate Ki67 scores were associated with poorer relapse-free survival than low Ki67 scores (P < .001 and P = .002, respectively). Furthermore, in the multivariate analyses of this subgroup, progression-free survival (PFS) was significantly longer in patients with low Ki67 scores than in patients with high Ki67 scores (hazard ratio, 0.387; 95% confidence interval, 0.233-0.643; P < .001). In the multivariate analyses, the Ki67 score was not significantly associated with PFS in the ER-positive and HER2-positive, ER-negative and HER2-positive, or ER-negative and HER2- negative subgroups. Conclusion: Our data demonstrated that low, intermediate, and high Ki67 scores have a prognostic value in breast cancer patients with ER-positive and HER2-negative tumors.
AB - We aimed to estimate the usefulness of scoring categories of IHC Ki67 as a prognostic factor for breast cancer subgroups. Our data demonstrated that Ki67 scores have a prognostic value in breast cancer patients with ERpositive and HER2-negative tumors. Background: Immunohistochemical (IHC) expression of Ki67 has a prognostic and predictive value for breast cancer, and the IHC Ki67 labeling index is estimated by counting the number of positive and negative cells. It has not been clarified whether IHC Ki67 estimated using a semiquantitative scoring system has a prognostic value. We aimed to estimate the usefulness of scoring categories of IHC Ki67 as a prognostic factor for breast cancer subgroups. Patients and Methods: We retrospectively identified patients in the Tokai University breast cancer database for whom IHC Ki67 data were available between January 1, 2000 and December 31, 2010. Survival curves were calculated using the Kaplan-Meier method and compared using the log-rank test. Results: Of the 1331 primary breast cancer patients included in the study, In patients with estrogen receptor (ER)-positive and HER2-negative tumors (n = 971), high and intermediate Ki67 scores were associated with poorer relapse-free survival than low Ki67 scores (P < .001 and P = .002, respectively). Furthermore, in the multivariate analyses of this subgroup, progression-free survival (PFS) was significantly longer in patients with low Ki67 scores than in patients with high Ki67 scores (hazard ratio, 0.387; 95% confidence interval, 0.233-0.643; P < .001). In the multivariate analyses, the Ki67 score was not significantly associated with PFS in the ER-positive and HER2-positive, ER-negative and HER2-positive, or ER-negative and HER2- negative subgroups. Conclusion: Our data demonstrated that low, intermediate, and high Ki67 scores have a prognostic value in breast cancer patients with ER-positive and HER2-negative tumors.
KW - ER
KW - Ki67
KW - Prognostic marker
KW - Proliferation
KW - Subgroups
UR - http://www.scopus.com/inward/record.url?scp=84922653564&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84922653564&partnerID=8YFLogxK
U2 - 10.1016/j.clbc.2013.12.013
DO - 10.1016/j.clbc.2013.12.013
M3 - Article
C2 - 24492237
AN - SCOPUS:84922653564
SN - 1526-8209
VL - 14
SP - 323-329.e3
JO - Clinical Breast Cancer
JF - Clinical Breast Cancer
IS - 5
ER -