Miyazono F, Metzger R, Warnecke-Eberz U, Baldus S E, Brabender J, Bollschweiler E, Doerfler W, Mueller R P, Dienes H P, Aikou T, Hoelscher A H, Schneider P M
Department of Visceral and Vascular Surgery, University of Cologne, Joseph-Stelzmann-Strasse 9, 50931 Cologne, Germany.
Br J Cancer. 2004 Aug 16;91(4):666-72. doi: 10.1038/sj.bjc.6601976.
We examined the potential of quantitative epidermal growth factor receptor (EGFR, synonym: c-erbB-1) and c-erbB-2 (synonym: HER2/neu) mRNA expression to predict minor or major histopathologic response to neoadjuvant radiochemotherapy (cis-platinum, 5-FU, 36 Gy), followed by radical surgical resection, in patients with oesophageal cancer. Tissue samples were collected by endoscopic biopsy prior to treatment. RNA was isolated from biopsies and quantitative real-time reverse transcriptase-polymerase chain reaction assays were performed to determine c-erbB-1 and c-erbB-2 mRNA expression. Relative expression (tumour/paired normal tissue ratio standardised for beta-actin) was calculated for EGFR and c-erbB-2 mRNA. Expression levels were correlated with the objective histopathologic response in resected specimens. Histomorphologic regression was defined as major response when resected specimens contained less than 10% of residual vital tumour cells, or in case a pathologically complete response was achieved. Expression of c-erbB-1 mRNA was not associated with the degree of histomorphological response. In contrast, the relative expression levels of c-erbB-2 mRNA >1 were not associated with major histopathologic responses (sensitivity 41.6%, specificity 100%), and 10 out of 36 (28%) patients could be unequivocally identified, whose tumours did not respond well to the delivered neoadjuvant radiochemotherapy (P<0.01). Quantitative expression levels of c-erbB-2, but not c-erbB-1 mRNA, in pretreatment biopsies appear to predict minor histopathologic response to our neoadjuvant radiochemotherapy protocol. This test could be used to prevent expensive, non effective and potentially harmful therapies in approximately one-fourth of our patients, and leads to a more individualised type of combined modality treatment.
我们研究了定量表皮生长因子受体(EGFR,同义词:c-erbB-1)和c-erbB-2(同义词:HER2/neu)mRNA表达预测食管癌患者对新辅助放化疗(顺铂、5-氟尿嘧啶、36 Gy)后进行根治性手术切除的轻微或主要组织病理学反应的潜力。治疗前通过内镜活检收集组织样本。从活检样本中分离RNA,并进行定量实时逆转录聚合酶链反应测定以确定c-erbB-1和c-erbB-2 mRNA表达。计算EGFR和c-erbB-2 mRNA的相对表达(针对β-肌动蛋白标准化的肿瘤/配对正常组织比率)。表达水平与切除标本中的客观组织病理学反应相关。当切除标本中残留的存活肿瘤细胞少于10%或实现病理完全缓解时,组织形态学消退被定义为主要反应。c-erbB-1 mRNA的表达与组织形态学反应程度无关。相比之下,c-erbB-2 mRNA>1的相对表达水平与主要组织病理学反应无关(敏感性41.6%,特异性100%),36例患者中有10例(28%)可以明确识别,其肿瘤对所给予的新辅助放化疗反应不佳(P<0.01)。治疗前活检中c-erbB-2而非c-erbB-1 mRNA的定量表达水平似乎可预测对我们的新辅助放化疗方案的轻微组织病理学反应。该检测可用于在约四分之一的患者中避免昂贵、无效且可能有害的治疗,并导致更个体化的联合治疗类型。