Prognostic Impact of Ki-67 Overexpression in Subgroups Categorized according to St. Gallen with Early Stage Breast Cancer

被引:11
作者
Matsubara, Nobuaki [1 ]
Mukai, Hirofumi [1 ]
Itoh, Kuniaki [1 ]
Nagai, Shunji [1 ]
机构
[1] Natl Canc Ctr Hosp E, Dept Oncol & Hematol, Chiba, Japan
关键词
Breast cancer; Ki-67; Prognostic factors; Proliferation; Tumor recurrence; HISTOLOGICAL GRADE; KI67; EXPRESSION; NUCLEAR ANTIGEN; IMAGE-ANALYSIS; PROLIFERATION; MARKER; CHEMOTHERAPY; THERAPY; CONSENSUS; EFFICACY;
D O I
10.1159/000334920
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Ki-67 overexpression has been reported to be related to a poor prognosis for early stage breast cancer. We analyzed whether Ki-67 has a prognostic impact on risk subgroups based on the recommendations at St. Gallen in 2007. Methods: To determine the impact of Ki-67 on each risk group, a retrospective analysis was performed in patients with breast cancer who underwent curative surgery. Ki-67 was examined by immunohistochemistry with a predefined cutoff level of 10%. Results: A total of 1,166 patients were eligible for this analysis. During the follow-up period, distant metastasis was observed in 164 patients (14.1%), and 80 patients (6.9%) died. Ki-67 overexpression (Ki-67 >= 10%) was identified as an independent prognostic factor for distant-metastatic-free survival (DFS) and overall survival (OS) by univariate and multivariate analysis. In the intermediate-risk group, the difference between Ki-67 overexpression and no overexpression was statistically significant in 5-year DFS (90.9 vs. 83.4%, p = 0.002) and OS (98.1 vs. 95.8%, p = 0.002). However, in both the low-and high-risk groups, Ki-67 overexpression was not an independent prognostic factor for either 5-year DFS or OS. Conclusions: Ki-67 overexpression indicates an unfavorable prognostic impact for DFS and OS. However, this impact is restricted only to those patients classified at intermediate risk. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:345 / 352
页数:8
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