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岭南现代临床外科 ›› 2016, Vol. 16 ›› Issue (02): 123-126.DOI: 10.3969/j.issn.1009-976X.2016.02.001

• 论著与临床研究 •    下一篇

Ki67、PgR在ER阳性且HER-2阴性乳腺癌Luminal分型中的意义

胡越 贾卫娟 谭翠 顾然 杨雅平 刘凤桃 苏逢锡   

  1. 中山大学孙逸仙纪念医院
  • 通讯作者: 苏逢锡

The significance of Ki67 and PgR in distinguishing ER-positive and HER-2-negative Luminal breast cancers

HU Yue, JIA Weijuan, TAN Cui, GU Ran, YANG Yaping, LIU Fengtao, SU Fengxi   

  • Received:2016-02-04 Revised:2016-01-18 Online:2016-04-20 Published:2016-04-20
  • Contact: SU Fengxi

摘要: 【摘要】 目的 探讨Ki67、PgR在Luminal型乳腺癌分型中的意义。方法〓回顾中山大学孙逸仙纪念医院2006~2012年入院治疗的ER阳性且HER-2阴性浸润性乳腺癌病人,收集病人的基本临床病理资料和随访结果。以无病生存时间为研究终点,采用Kaplan-Meier检验和Cox回归进行生存分析。结果〓共964例浸润性乳腺癌入组。K-M单因素分析结果表明,Ki67 14%具有统计学意义,而PgR 20%仅在早期生存分析时具有统计学意义。Cox多因素分析结果表明,Ki67是无病生存的独立预测因子,而PgR却没有统计学意义。Ki67低表达且PgR低表达的亚组较Ki67高表达且PgR高表达的亚组有着不一致的生存结果。结论〓在ER阳性且HER-2阴性乳腺癌Luminal分型中,不能将PgR和Ki67置于同等重要的位置,对于Ki67低表达且PgR低表达的乳腺癌,需要结合其它临床病理资料或多基因分析。

关键词: Ki67, PgR, 乳腺癌, Luminal A, Luminal B, 无病生存

Abstract: 【Abstract】〓Objective〓The objective of this study was to analyze the prognostic significance of Ki67 and PgR in distinguishing Luminal breast cancers. Methods〓Patients with ER-positive and HER-2-negative invasive breast cancer who were treated from 2006 to 2012, were selected by searching breast cancer registries at Sun Yat-sen Memorial Hospital..Clinicopathologic characteristics and prognoses were collected. The primary end point was DFS (disease free survival) which was analyzed by Kaplan-Meier curve with log rank test or Breslow test. Cox proportional hazards model was used to balance the risk factors for prognosis. Results〓A total of 964 patients with invasive breast cancer were eligible for inclusion in this study. Ki67 was found to be of prognostic significance in univariate analysis and multivariate analysis, but PgR was not an independent risk factor. Patients with low-Ki67-level and low-PgR level had different prognoses with high-Ki67-level and high-PgR-level subtype. Conclusion〓In order to optimize management of ER-positive and HER-2-negative patients, we need to consult other clinicopathologic characteristics or multi-gene assay, especially for low-Ki67-level and low-PgR level subtype.

Key words: Ki67, PgR, Breast cancer, Luminal A, Luminal B, Disease free survival

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