Kimura H, Suminoe M, Kasahara K, Sone T, Araya T, Tamori S, Koizumi F, Nishio K, Miyamoto K, Fujimura M, Nakao S
Department of Respiratory Medicine, Kanazawa University Hospital, Takara-machi 13-1, Kanazawa, Ishikawa, Japan.
Br J Cancer. 2007 Sep 17;97(6):778-84. doi: 10.1038/sj.bjc.6603949.
The aim of this study was to evaluate the usefulness of EGFR mutation status in serum DNA as a means of predicting a benefit from gefitinib (IRESSA) therapy in Japanese patients with non-small cell lung cancer (NSCLC). We obtained pairs of tumour and serum samples from 42 patients treated with gefitinib. EGFR mutation status was determined by a direct sequencing method and by Scorpion Amplification Refractory Mutation System (ARMS) technology. EGFR mutations were detected in the tumour samples of eight patients and in the serum samples of seven patients. EGFR mutation status in the tumours and serum samples was consistent in 39 (92.9%) of the 42 pairs. EGFR mutations were strong correlations between both EGFR mutation status in the tumour samples and serum samples and objective response to gefitinib (P<0.001). Median progression-free survival time was significantly longer in the patients with EGFR mutations than in the patients without EGFR mutations (194 vs 55 days, P=0.016, in tumour samples; 174 vs 58 days, P=0.044, in serum samples). The results suggest that it is feasible to use serum DNA to detect EGFR mutation, and that it's potential as a predictor of response to, and survival on gefitinib is worthy of further evaluation.
本研究旨在评估血清DNA中表皮生长因子受体(EGFR)突变状态作为预测日本非小细胞肺癌(NSCLC)患者接受吉非替尼(易瑞沙)治疗是否获益的一种手段的有效性。我们从42例接受吉非替尼治疗的患者中获取了肿瘤和血清样本对。EGFR突变状态通过直接测序法和蝎形扩增难治突变系统(ARMS)技术来确定。在8例患者的肿瘤样本和7例患者的血清样本中检测到EGFR突变。42对样本中,有39对(92.9%)肿瘤样本和血清样本中的EGFR突变状态一致。肿瘤样本和血清样本中的EGFR突变状态与对吉非替尼的客观反应之间均存在强相关性(P<0.001)。EGFR突变患者的无进展生存期(PFS)中位数显著长于无EGFR突变的患者(肿瘤样本中为194天对55天,P=0.016;血清样本中为174天对58天,P=0.044)。结果表明,利用血清DNA检测EGFR突变是可行的,其作为吉非替尼反应和生存预测指标的潜力值得进一步评估。