Department of Internal Medicine, College of Medicine, National Taiwan University Hospital Yun-Lin Branch, Yun-Lin, Taiwan.
PLoS One. 2011;6(8):e23303. doi: 10.1371/journal.pone.0023303. Epub 2011 Aug 9.
Epidermal growth factor receptor (EGFR) is a novel target for therapy in subsets of non-small cell lung cancer, especially adenocarcinoma. Tumors with EGFR mutations showed good response to EGFR tyrosine kinase inhibitors (TKIs). We aimed to identify the discriminating capacity of immunohistochemical (IHC) scoring to detect L858R and E746-A750 deletion mutation in lung adenocarcinoma patients and predict EGFR TKIs response. Patients with surgically resected lung adenocarcinoma were enrolled. EGFR mutation status was genotyped by PCR and direct sequencing. Mutation-specific antibodies for L858R and E746-A750 deletion were used for IHC staining. Receiver operating characteristic (ROC) curves were used to determine the capacity of IHC, including intensity and/or quickscore (Q score), in differentiating L858R and E746-A750 deletion. We enrolled 143 patients during September 2000 to May 2009. Logistic-regression-model-based scoring containing both L858R Q score and total EGFR expression Q score was able to obtain a maximal area under the curve (AUC: 0.891) to differentiate the patients with L858R. Predictive model based on IHC Q score of E746-A750 deletion and IHC intensity of total EGFR expression reached an AUC of 0.969. The predictive model of L858R had a significantly higher AUC than L858R intensity only (p = 0.036). Of the six patients harboring complex EGFR mutations with classical mutation patterns, five had positive IHC staining. For EGFR TKI treated cancer recurrence patients, those with positive mutation-specific antibody IHC staining had better EGFR TKI response (p = 0.008) and longer progression-free survival (p = 0.012) than those without. In conclusion, total EGFR expression should be included in the IHC interpretation of L858R. After adjusting for total EGFR expression, the scoring method decreased the false positive rate and increased diagnostic power. According to the scoring method, the IHC method is useful to predict the clinical outcome and refine personalized therapy.
表皮生长因子受体 (EGFR) 是某些非小细胞肺癌,特别是腺癌的新型治疗靶点。具有 EGFR 突变的肿瘤对 EGFR 酪氨酸激酶抑制剂 (TKI) 反应良好。我们旨在确定免疫组织化学 (IHC) 评分对检测肺腺癌患者中 L858R 和 E746-A750 缺失突变的区分能力,并预测 EGFR TKI 反应。入组接受手术切除的肺腺癌患者。通过 PCR 和直接测序对 EGFR 突变状态进行基因分型。使用突变特异性 L858R 和 E746-A750 缺失抗体进行 IHC 染色。使用受试者工作特征 (ROC) 曲线确定 IHC,包括强度和/或快速评分 (Q 评分),在区分 L858R 和 E746-A750 缺失方面的能力。我们于 2000 年 9 月至 2009 年 5 月期间入组了 143 名患者。基于逻辑回归模型的评分包含 L858R Q 评分和总 EGFR 表达 Q 评分,能够获得区分 L858R 的最大曲线下面积 (AUC:0.891)。基于 E746-A750 缺失的 IHC Q 评分和总 EGFR 表达的 IHC 强度的预测模型达到 AUC 为 0.969。基于 L858R 的预测模型的 AUC 明显高于仅基于 L858R 强度的预测模型 (p = 0.036)。在具有经典突变模式的 6 名具有复杂 EGFR 突变的患者中,有 5 名具有阳性 IHC 染色。对于接受 EGFR TKI 治疗的癌症复发患者,那些具有阳性突变特异性抗体 IHC 染色的患者具有更好的 EGFR TKI 反应 (p = 0.008) 和更长的无进展生存期 (p = 0.012)。总之,应将总 EGFR 表达纳入 L858R 的 IHC 解释中。在调整总 EGFR 表达后,评分方法降低了假阳性率并提高了诊断能力。根据评分方法,IHC 方法可用于预测临床结果并完善个体化治疗。