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表皮生长因子受体基因多态性预测 EGFR 突变阳性非小细胞肺癌患者接受厄洛替尼治疗的预后改善。

EGFR Gene Polymorphism Predicts Improved Outcome in Patients With EGFR Mutation-positive Non-small cell Lung Cancer Treated With Erlotinib.

机构信息

Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.

Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Clin Lung Cancer. 2019 May;20(3):161-166.e1. doi: 10.1016/j.cllc.2019.02.011. Epub 2019 Feb 26.

Abstract

BACKGROUND

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.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

患者和方法

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。

结果

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。

结论

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。

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