Rudas M, Gnant M F, Mittlböck M, Neumayer R, Kummer A, Jakesz R, Reiner G, Reiner A
Institute for Clinical Pathology, University of Vienna, Austria.
Breast Cancer Res Treat. 1994;32(2):165-75. doi: 10.1007/BF00665767.
In situ determination of proliferative activity was performed on 184 consecutive primary invasive breast cancers. Methods used were monoclonal antibody Ki-67 in immunohistochemistry and thymidine labeling index. Tumor proliferation correlated between both methods (p = 0.0001). For thymidine labeling index and Ki-67, respectively, significant correlations existed with histologic tumour grade and steroid hormone receptors (Tumor grade: TLI p = 0.0001; Ki-67 p = 0.0001. ER-ICA: TLI = 0.0001; Ki-67 p = 0.014. PgR-ICA: TLI p = 0.0001; Ki-67 p = 0.0008). For thymidine labeling index a significant correlation was demonstrated for overall survival (p = 0.001) and recurrence free survival (p = 0.01). No statistical significance was observed for clinical outcome and Ki-67 (overall survival p = 0.18; recurrence free survival p = 0.1). None of the factors, TLI or Ki-67, was an independent prognostic factor as demonstrated by multivariate analysis.
对184例连续的原发性浸润性乳腺癌进行了增殖活性的原位测定。使用的方法是免疫组织化学中的单克隆抗体Ki-67和胸腺嘧啶核苷标记指数。两种方法之间的肿瘤增殖具有相关性(p = 0.0001)。对于胸腺嘧啶核苷标记指数和Ki-67,分别与组织学肿瘤分级和类固醇激素受体存在显著相关性(肿瘤分级:TLI p = 0.0001;Ki-67 p = 0.0001。ER-ICA:TLI = 0.0001;Ki-67 p = 0.014。PgR-ICA:TLI p = 0.0001;Ki-67 p = 0.0008)。对于胸腺嘧啶核苷标记指数,总生存期(p = 0.001)和无复发生存期(p = 0.01)显示出显著相关性。未观察到临床结局与Ki-67之间的统计学意义(总生存期p = 0.18;无复发生存期p = 0.1)。多变量分析表明,TLI或Ki-67这些因素均不是独立的预后因素。