Department of Oncology, Clinical Sciences, Lund University and Lund University Hospital, SE 221 85 Lund, Sweden.
Mod Pathol. 2010 Feb;23(2):251-9. doi: 10.1038/modpathol.2009.167. Epub 2009 Nov 20.
The aim of this study was to evaluate the prognostic value of Ki67 in relation to established prognostic factors in lymph node-negative breast cancer, and furthermore, whether the prognostic impact was dependent on estrogen receptor (ER) status and histological grade. In 200 premenopausal patients, with 5 years of follow-up, Ki67 was determined on tissue microarrays. In univariate analysis, Ki67 (< or = 20 vs >20%) was a prognostic factor for distant disease-free survival (hazard ratio: 2.7, 95% confidence interval: 1.3-5.4, P=0.005) and overall survival (hazard ratio: 4.9, 95% confidence interval: 1.7-14, P=0.003). When stratifying for ER status and histological grade, Ki67 was a significant prognostic factor for distant disease-free survival and overall survival only in the ER-positive group, and only in patients with histological grade 2, respectively. In multivariate analysis, human epidermal growth factor receptor 2 and age were independent prognostic factors for distant disease-free survival, whereas Ki67, histological grade, and tumor size were not. Ki67 was, however, an independent prognostic factor in the 87% of the patients who had not received adjuvant medical treatment. Agreement between the three readers was very good (kappa-values: 0.83-0.88). Furthermore, Ki67 was a significant prognostic factor for all three investigators (hazard ratio: 2.7-3.2). This study shows that Ki67 is a prognostic factor in node-negative breast cancer. It is noteworthy that the prognostic information of Ki67 is restricted to ER-positive patients, and to patients with histological grade 2. Taken together, Ki67, as an easily assessed and reproducible proliferation factor, may be an alternative or complement to histological grade as a prognostic tool and for selection of adjuvant treatment.
本研究旨在评估 Ki67 在淋巴结阴性乳腺癌中与已建立的预后因素的相关性,并进一步评估其预后影响是否依赖于雌激素受体 (ER) 状态和组织学分级。在 200 例有 5 年随访的绝经前患者中,使用组织微阵列测定 Ki67。在单因素分析中,Ki67(≤20% vs >20%)是远处无病生存的预后因素(风险比:2.7,95%置信区间:1.3-5.4,P=0.005)和总生存(风险比:4.9,95%置信区间:1.7-14,P=0.003)。当按 ER 状态和组织学分级分层时,Ki67 仅在 ER 阳性组,且仅在组织学分级为 2 级的患者中,是远处无病生存和总生存的显著预后因素。在多因素分析中,人表皮生长因子受体 2 和年龄是远处无病生存的独立预后因素,而 Ki67、组织学分级和肿瘤大小则不是。然而,在未接受辅助治疗的 87%的患者中,Ki67 是独立的预后因素。三位读者之间的一致性非常好(kappa 值:0.83-0.88)。此外,Ki67 是所有三位研究者的显著预后因素(风险比:2.7-3.2)。本研究表明,Ki67 是淋巴结阴性乳腺癌的预后因素。值得注意的是,Ki67 的预后信息仅限于 ER 阳性患者和组织学分级为 2 级的患者。总之,Ki67 作为一种易于评估和可重复的增殖因子,可能是组织学分级作为预后工具和辅助治疗选择的替代或补充。