Department of Pathology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Department of Breast Surgery, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Breast Cancer Res Treat. 2017 Nov;166(1):77-84. doi: 10.1007/s10549-017-4397-z. Epub 2017 Jul 15.
Accurate testing of the status of human epidermal growth factor receptor type 2 (HER2) is a prerequisite for HER2-directed therapy. The American Society of Clinical Oncology (ASCO) and the College of American Pathologists (CAP) published joint guideline recommendations for HER2 testing in breast cancer in 2007 and it was updated in 2013. We compared the HER2 gene amplification status based on these two guidelines and analyzed the molecular characteristics of the equivocal cases.
A total of 1894 patient samples were analyzed for both immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH). HER2 FISH amplification was examined and re-assessed using 2013 guidelines.
According to the 2013 ASCO/CAP recommendations, 763 (40.3%) cases were classified as HER2 positive compared with 729 (38.5%) cases defined by 2007 guidelines. There was a significant increase of 6.1% in the proportion of HER2 FISH equivocal cases that were interpreted using ASCO/CAP 2013 (7.3%) compared with 2007 (1.2%) guidelines (P < 0.001). Of 138 FISH equivocal cases defined by 2013 guidelines, 125 cases were IHC2+ and 13 cases were IHC1+. These 125 cases included 4 double equivocal cases which were defined as equivocal by both 2007 and 2013 guidelines and 121 cases whose status was changed from negative defined by 2007 guidelines to equivocal defined by 2013 guidelines. Compared with luminal A type and luminal B type respectively, these 121 equivocal cases demonstrated no significant difference with luminal B type in T stage and N stage (P = 0.192, P = 0.421). When we divided the luminal B type into two parts that included HER2 negative cases and HER2 positive cases, the equivocal cases also showed no significant difference with these two subtypes in T stage and N stage.
Our study suggested that implementation of the revised ASCO/CAP 2013 guidelines resulted in an increase of 1.7% in overall HER2 positivity rate and of 6.1% in equivocal cases. Pathological analysis revealed that these equivocal cases exhibit similar biological behavior with luminal B type tumors. Clinical utility data on targeted therapy in equivocal patients should be further investigated.
准确检测人类表皮生长因子受体 2(HER2)的状态是 HER2 靶向治疗的前提。美国临床肿瘤学会(ASCO)和美国病理学家协会(CAP)于 2007 年发布了乳腺癌 HER2 检测的联合指南建议,并于 2013 年进行了更新。我们比较了基于这两个指南的 HER2 基因扩增状态,并分析了不确定病例的分子特征。
共分析了 1894 例患者的免疫组织化学(IHC)和荧光原位杂交(FISH)结果。使用 2013 年指南检查和重新评估 HER2 FISH 扩增。
根据 2013 年 ASCO/CAP 建议,763 例(40.3%)病例被归类为 HER2 阳性,而 2007 年指南定义的 729 例(38.5%)病例有所增加。使用 ASCO/CAP 2013 年指南(7.3%)与 2007 年指南(1.2%)相比,HER2 FISH 不确定病例的比例显著增加了 6.1%(P<0.001)。在 2013 年指南定义的 138 例 FISH 不确定病例中,125 例为 IHC2+,13 例为 IHC1+。这 125 例包括 4 例双不确定病例,这 4 例病例在 2007 年和 2013 年指南中均被定义为不确定,121 例病例的状态从 2007 年指南定义的阴性变为不确定。与 luminal A 型和 luminal B 型相比,这些不确定的 121 例病例在 T 分期和 N 分期上与 luminal B 型无显著差异(P=0.192,P=0.421)。当我们将 luminal B 型分为包括 HER2 阴性和 HER2 阳性病例的两部分时,不确定病例在 T 分期和 N 分期上与这两个亚组也无显著差异。
我们的研究表明,实施修订后的 ASCO/CAP 2013 指南导致总体 HER2 阳性率增加了 1.7%,不确定病例增加了 6.1%。病理分析显示,这些不确定病例的生物学行为与 luminal B 型肿瘤相似。应进一步研究不确定患者靶向治疗的临床应用数据。