Department of Surgery and Comprehensive Cancer Center, Medical University Vienna, Vienna, Austria.
Br J Cancer. 2013 Dec 10;109(12):2959-64. doi: 10.1038/bjc.2013.671. Epub 2013 Oct 24.
ER+/HER2- breast cancers have a proclivity for late recurrence. A personalised estimate of relapse risk after 5 years of endocrine treatment can improve patient selection for extended hormonal therapy.
A total of 1702 postmenopausal ER+/HER2- breast cancer patients from two adjuvant phase III trials (ABCSG6, ABCSG8) treated with 5 years of endocrine therapy participated in this study. The multigene test EndoPredict (EP) and the EPclin score (which combines EP with tumour size and nodal status) were predefined in independent training cohorts. All patients were retrospectively assigned to risk categories based on gene expression and on clinical parameters. The primary end point was distant metastasis (DM). Kaplan-Meier method and Cox regression analysis were used in an early (0-5 years) and late time interval (>5 years post diagnosis).
EP is a significant, independent, prognostic parameter in the early and late time interval. The expression levels of proliferative and ER signalling genes contribute differentially to the underlying biology of early and late DM. The EPclin stratified 64% of patients at risk after 5 years into a low-risk subgroup with an absolute 1.8% of late DM at 10 years of follow-up.
The EP test provides additional prognostic information for the identification of early and late DM beyond what can be achieved by combining the commonly used clinical parameters. The EPclin reliably identified a subgroup of patients who have an excellent long-term prognosis after 5 years of endocrine therapy. The side effects of extended therapy should be weighed against this projected outcome.
ER+/HER2- 乳腺癌有复发晚的倾向。在接受内分泌治疗 5 年后,对复发风险进行个体化估计可以改善延长激素治疗的患者选择。
本研究共纳入了来自两项辅助 III 期试验(ABCSG6、ABCSG8)的 1702 例绝经后 ER+/HER2- 乳腺癌患者,这些患者接受了 5 年的内分泌治疗。多基因检测 EndoPredict(EP)和 EPclin 评分(将 EP 与肿瘤大小和淋巴结状态相结合)在独立的训练队列中预先确定。所有患者均根据基因表达和临床参数回顾性地分配到风险类别。主要终点为远处转移(DM)。Kaplan-Meier 法和 Cox 回归分析用于早期(0-5 年)和晚期(诊断后>5 年)时间间隔。
EP 是早期和晚期时间间隔的一个显著、独立的预后参数。增殖和 ER 信号基因的表达水平对早期和晚期 DM 的潜在生物学有不同的贡献。EPclin 将 5 年后有风险的 64%的患者分为低风险亚组,这些患者在 10 年随访中晚期 DM 的绝对发生率为 1.8%。
EP 检测提供了额外的预后信息,可以在联合使用常用临床参数的基础上,进一步识别早期和晚期 DM。EPclin 可靠地识别了一组在接受 5 年内分泌治疗后具有良好长期预后的患者。应权衡延长治疗的副作用与这一预期结果。