Parise Carol A, Caggiano Vincent
Sutter Institute for Medical Research, 2801 Capitol Avenue, Suite 400, Sacramento, CA 95816, USA.
J Cancer Epidemiol. 2014;2014:469251. doi: 10.1155/2014/469251. Epub 2014 May 26.
Introduction. ER, PR, and HER2 are routinely available in breast cancer specimens. The purpose of this study is to contrast breast cancer-specific survival for the eight ER/PR/HER2 subtypes with survival of an immunohistochemical surrogate for the molecular subtype based on the ER/PR/HER2 subtypes and tumor grade. Methods. We identified 123,780 cases of stages 1-3 primary female invasive breast cancer from California Cancer Registry. The surrogate classification was derived using ER/PR/HER2 and tumor grade. Kaplan-Meier survival analysis and Cox proportional hazards modeling were used to assess differences in survival and risk of mortality for the ER/PR/HER2 subtypes and surrogate classification within each stage. Results. The luminal B/HER2- surrogate classification had a higher risk of mortality than the luminal B/HER2+ for all stages of disease. There was no difference in risk of mortality between the ER+/PR+/HER2- and ER+/PR+/HER2+ in stage 3. With one exception in stage 3, the ER-negative subtypes all had an increased risk of mortality when compared with the ER-positive subtypes. Conclusions. Assessment of survival using ER/PR/HER2 illustrates the heterogeneity of HER2+ subtypes. The surrogate classification provides clear separation in survival and adjusted mortality but underestimates the wide variability within the subtypes that make up the classification.
引言。雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2(HER2)在乳腺癌标本中常规可得。本研究的目的是对比基于ER/PR/HER2亚型和肿瘤分级的8种ER/PR/HER2分子亚型的乳腺癌特异性生存率与免疫组化替代分子亚型的生存率。方法。我们从加利福尼亚癌症登记处识别出123780例1-3期原发性女性浸润性乳腺癌病例。替代分类是使用ER/PR/HER2和肿瘤分级得出的。采用Kaplan-Meier生存分析和Cox比例风险模型来评估各期内ER/PR/HER2亚型和替代分类在生存率和死亡风险上的差异。结果。在疾病的所有阶段,管腔B/HER2-替代分类的死亡风险均高于管腔B/HER2+。在3期,ER+/PR+/HER2-和ER+/PR+/HER2+的死亡风险没有差异。除3期有一个例外情况外,与ER阳性亚型相比,ER阴性亚型的死亡风险均增加。结论。使用ER/PR/HER2评估生存率说明了HER2阳性亚型的异质性。替代分类在生存率和校正死亡率方面有明显区分,但低估了构成该分类的各亚型内的广泛变异性。