Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Clin Lung Cancer. 2019 May;20(3):161-166.e1. doi: 10.1016/j.cllc.2019.02.011. Epub 2019 Feb 26.
Patients with advanced-stage non-small cell lung cancer with epidermal growth factor receptor (EGFR) mutations are successfully treated with tyrosine kinase inhibitors (TKIs). However, treatment outcome varies significantly. Previously, we found the polymorphism 181946C>T (rs2293347) located in exon 25 of the EGFR gene to be a predictor of improved outcome. However, these data were based on a subgroup analysis. Furthermore, other minor studies have found conflicting data. Thus, the aim of this study was to demonstrate the association of 181946C>T with clinical outcome in an independent cohort of EGFR-mutated patients treated with erlotinib.
Seventy-five patients were prospectively enrolled. Blood samples were collected, and genotype for 181946C>T was determined by allele-specific polymerase chain reaction. Genotype was correlated with outcome.
In 73 patients, 181946C>T was successfully measured. Patients harboring the 181946CT genotype had a significantly longer median progression-free survival compared with patients harboring the 181946CC genotype (49.9 months [95% confidence interval (CI), 5.9-93.9 months] versus 11.1 months (95% CI, 7.4-14.9 months); P = .020). Moreover, a significantly longer median overall survival of 65.6 months (95% CI, 11.0-120.3 months) versus 31.2 months (95% CI, 10.9-51.6 months) was found (P = .019). Both results remained significant in a multivariate analysis adjusting for potential confounders.
We demonstrate that the 181946C>T polymorphism is a significant predictor of prolonged progression-free survival and overall survival in an independent cohort of EGFR mutation-positive patients treated with erlotinib. The polymorphism could be an important predictor of treatment response in these patients. A large multicenter cohort study involving other concurrent genetic alterations is warranted.
表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌患者经酪氨酸激酶抑制剂(TKI)治疗可取得显著疗效,但治疗效果存在显著差异。既往研究发现,EGFR 基因第 25 外显子的 181946C>T(rs2293347)多态性可预测患者的获益。但上述数据基于亚组分析,且其他少量研究结果存在矛盾。本研究旨在通过一项独立的 EGFR 突变患者接受厄洛替尼治疗的队列研究,进一步验证 181946C>T 与临床结局的相关性。
前瞻性纳入 75 例患者,采集血样,采用等位基因特异性聚合酶链反应检测 181946C>T 基因型,分析基因型与结局的相关性。
73 例患者成功检测到 181946C>T 基因型。携带 181946CT 基因型的患者中位无进展生存期显著长于携带 181946CC 基因型的患者(49.9 个月[95%置信区间(CI):5.9-93.9 个月] vs. 11.1 个月[95%CI:7.4-14.9 个月];P=0.020),中位总生存期也显著延长(65.6 个月[95%CI:11.0-120.3 个月] vs. 31.2 个月[95%CI:10.9-51.6 个月];P=0.019)。多变量分析校正潜在混杂因素后,上述结果仍有统计学意义。
本研究证实,在接受厄洛替尼治疗的 EGFR 突变阳性患者的独立队列中,181946C>T 多态性是无进展生存期和总生存期的显著预测因素。该多态性可能是此类患者治疗反应的重要预测因素,有必要开展涉及其他共突变的多中心大样本队列研究。