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[表皮生长因子受体酪氨酸激酶抑制剂疗效与晚期肺鳞状细胞癌中EGFR突变的相关性]

[Correlation between the efficacy of epidermal growth factor receptor tyrosine kinase inhibitors and EGFR mutations in advanced squamous cell lung cancer].

作者信息

Duan Jian-chun, An Tong-tong, Wu Mei-na, Yang Lu, Bai Hua, Wang Zhi-jie, Wang Yu-yan, Zhuo Ming-lei, Zhao Jun, Wang Shu-hang, Wang Jie

机构信息

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Thoracic Oncology, Peking University School of Oncology, Beijing Cancer Hospital & Institute, Beijing 100142, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2012 May;35(5):323-8.

Abstract

OBJECTIVE

To investigate the frequency of epidermal growth factor receptor (EGFR) mutations and their correlation with the efficacy of tyrosine kinase inhibitors (EGFR-TKI) in advanced squamous cell lung cancer.

METHODS

This retrospective study enrolled 79 patients with advanced squamous cell lung cancer who received EGFR-TKI at Department of Thoracic Medical Oncology in Peking University Cancer Hospital from June 2004 to June 2011. Among them, 67 patients had tissue and/or plasma EGFR exon 19 and 21 mutation detection in order to make an analysis on the relationship between EGFR mutation and the TKI's effect.

RESULTS

The disease control rate (DCR) was 56% in all the patients. The median progression free survival (mPFS) and median overall survival (mOS) was 3.7 months (95%CI: 2.0 - 5.0) and 11.5 months (95%CI: 6.6 - 14.2), respectively. Of the 67 patients who received EGFR mutation detection, there were 31 patients harboring EGFR-mutation, for whom the DCR was 71% (22/31), and mPFS and mOS was 6.3 months (95%CI: 2.2 - 10.0) and 13.5 months (95%CI: 7.3 - 18.6) respectively. 36 patients' EGFR status were wild type, for whom the DCR was 44% (16/36), mPFS and mOS was 2.2 months (95%CI: 1.1 - 4.0) and 6.4 months (95%CI: 4.0 - 12.0). There were 17 patients who received erlotinib and 7 patients who received gefitinib as second or more line treatment. mPFS and mOS were 7.9 months and 15.8 months in the erlotinib group, respectively; and the mPFS and mOS were both 6.3 months in gefitinib group; the difference between the 2 groups did not reach statistical significance. Cox-regression analysis showed that EGFR mutation was significantly correlated with PFS and OS (P < 0.05, respectively). EGFR mutation was significantly correlated with DCR by Chi-square test, P < 0.05.

CONCLUSIONS

EGFR mutation was a predictor for advanced squamous cell lung cancer to EGFR-TKI. However, the effect was inferior in advanced squamous cell lung cancer as compared to lung adenocarcinoma. Erlotinib tended to be superior to gefitinib.

摘要

目的

探讨晚期肺鳞癌中表皮生长因子受体(EGFR)突变的频率及其与酪氨酸激酶抑制剂(EGFR-TKI)疗效的相关性。

方法

本回顾性研究纳入了2004年6月至2011年6月在北京大学肿瘤医院胸内肿瘤内科接受EGFR-TKI治疗的79例晚期肺鳞癌患者。其中67例患者进行了组织和/或血浆EGFR第19和21外显子突变检测,以分析EGFR突变与TKI疗效之间的关系。

结果

所有患者的疾病控制率(DCR)为56%。中位无进展生存期(mPFS)和中位总生存期(mOS)分别为3.7个月(95%CI:2.0 - 5.0)和11.5个月(95%CI:6.6 - 14.2)。在67例接受EGFR突变检测的患者中,有31例存在EGFR突变,其DCR为71%(22/31),mPFS和mOS分别为6.3个月(95%CI:2.2 - 10.0)和13.5个月(95%CI:7.3 - 18.6)。36例患者的EGFR状态为野生型,其DCR为44%(16/36),mPFS和mOS分别为2.2个月(95%CI:1.1 - 4.0)和6.4个月(95%CI:4.0 - 12.0)。有17例患者接受厄洛替尼作为二线或更后线治疗,7例患者接受吉非替尼作为二线或更后线治疗。厄洛替尼组的mPFS和mOS分别为7.9个月和15.8个月;吉非替尼组的mPFS和mOS均为6.3个月;两组之间的差异未达到统计学意义。Cox回归分析显示,EGFR突变与PFS和OS均显著相关(P均<0.05)。经卡方检验,EGFR突变与DCR显著相关,P<0.05。

结论

EGFR突变是晚期肺鳞癌对EGFR-TKI治疗的一个预测指标。然而,与肺腺癌相比,其在晚期肺鳞癌中的疗效较差。厄洛替尼的疗效倾向于优于吉非替尼。

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