Abdelrahman Aziza E, Rashed Hayam E, Abdelgawad Mohamed, Abdelhamid Mohamed I
Pathology Department, Faculty of Medicine, Zagazig University, Egypt.
Pathology Department, Faculty of Medicine, Zagazig University, Egypt.
Ann Diagn Pathol. 2017 Jun;28:43-53. doi: 10.1016/j.anndiagpath.2017.01.009. Epub 2017 Feb 4.
Triple-negative breast cancer (TNBC) has an aggressive behavior and limited therapeutic options due to lack of targeted therapy. We aimed in this study to assess the immunohistochemical expression of EGFR and cytokeratin 5/6 and their ability to predict survival and response to neoadjuvant chemotherapy (NAC) among triple-negative breast cancer patients. Thirty-five cases with TNBC were studied by immunohistochemistry for EGFR and CK5/6 expression. Data on overall survival (OS), disease-free survival (DFS) and response to NAC were collected. The resulted data were statistically analyzed. Invasive carcinoma of no special type (NST) was the predominant histopathological type (80%). The commonest histological grade was grade II-III (88.6%). About 57.1% of TNBC cases were CK5/6-positive, and 71.4% were EGFR-positive. EGFR expression showed a significant association with tumor grade and axillary lymph node metastasis (p=0.006, 0.016 respectively). EGFR expression was related to unfavorable response to NAC (p=0.036), poor OS (p=0.002) and poor DFS (p=0.003). CK5/6 expression showed a significant association with tumor grade, unfavorable response to NAC, poor OS & DFS (p=0.007, 0.048, <0.001, 0.043 respectively). Immunohistochemical expression of EGFR and/or CK5/6 showed a high significant association with an unfavorable response to NAC, poor DFS &OS (p=0.010, 0.012, 0.030 respectively).
EGFR and CK5/6 are adverse prognostic markers in TNBC. EGFR and CK5/6 expression could serve as biomarkers for identifying TNBC patients with poor survival that are unlikely to benefit from neoadjuvant chemotherapy. So, targeted therapy against EGFR may be a hopeful therapy for TNBC with NAC resistance.
三阴性乳腺癌(TNBC)具有侵袭性,且由于缺乏靶向治疗,治疗选择有限。本研究旨在评估三阴性乳腺癌患者中表皮生长因子受体(EGFR)和细胞角蛋白5/6的免疫组化表达及其预测生存和对新辅助化疗(NAC)反应的能力。通过免疫组化研究了35例三阴性乳腺癌患者的EGFR和CK5/6表达。收集了总生存(OS)、无病生存(DFS)和对NAC反应的数据。对所得数据进行统计学分析。非特殊类型浸润性癌(NST)是主要的组织病理学类型(80%)。最常见的组织学分级为II - III级(88.6%)。约57.1%的三阴性乳腺癌病例CK5/6呈阳性,71.4%的病例EGFR呈阳性。EGFR表达与肿瘤分级和腋窝淋巴结转移显著相关(分别为p = 0.006、0.016)。EGFR表达与对NAC的不良反应相关(p = 0.036),与较差的总生存(p = 0.002)和无病生存(p = 0.003)相关。CK5/6表达与肿瘤分级、对NAC的不良反应、较差的总生存和无病生存显著相关(分别为p = 0.007、0.048、<0.001、0.043)。EGFR和/或CK5/6的免疫组化表达与对NAC的不良反应、较差的无病生存和总生存高度显著相关(分别为p = 0.010、0.012、0.030)。
EGFR和CK5/6是三阴性乳腺癌的不良预后标志物。EGFR和CK5/6表达可作为生物标志物,用于识别生存较差且不太可能从新辅助化疗中获益的三阴性乳腺癌患者。因此,针对EGFR的靶向治疗可能是对NAC耐药的三阴性乳腺癌的一种有前景的治疗方法。