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肺癌手术切除样本与非手术切除样本中EGFR、KRAS、BRAF、EML4-ALK和ROS1的临床特征及突变状态

Clinical features and mutation status of EGFR, KRAS, BRAF, EML4-ALK and ROS1 between surgical resection samples and non surgical resection samples in lung cancer.

作者信息

Li Wentao, Qu Jichen, Xu Zhifei

机构信息

1 Department of Thoracic Surgery, Shanghai pulmonary hospital, Tongji University School of Medicine, Shanghai 200433, China ; 2 Department of Thoracic Surgery, Shanghai Changzheng hospital Affiliated to Shanghai Second Military University, Shanghai 200061, China.

出版信息

J Thorac Dis. 2015 May;7(5):875-80. doi: 10.3978/j.issn.2072-1439.2015.04.49.

Abstract

BACKGROUND

Target therapy is the first-line treatment in lung cancer. The testing of driver gene mutations is crucial for decision of treatment. Many lung cancer patients are in advanced grade, and lose the chance of operation.

METHODS

The tissue used to perform mutation testing is only from biopsy. In order to analysis the difference between surgical resection samples (SRSs) and non-surgical resection samples (NSRSs), 1,357 surgical tissues and 145 biopsy samples histopathologically diagnosed with lung cancer were collected to detect the mutation status of EGFR, KRAS, BRAF, EML4-ALK and ROS1 in this study.

RESULTS

There were no significant differences of age, gender, and histological type between the two group patients we collected; however, the significant difference was present in grade. More early stage patients were in the surgical group, but more advanced stage lung cancer patients were in non surgical group. In the mutation analysis, we also found no significant differences in all driver genes we detected between the two groups.

CONCLUSIONS

Both surgical resection samples and biopsy samples could be used to perform the testing the driver gene mutation.

摘要

背景

靶向治疗是肺癌的一线治疗方法。驱动基因突变检测对于治疗决策至关重要。许多肺癌患者处于晚期,失去了手术机会。

方法

用于进行突变检测的组织仅来自活检。为了分析手术切除样本(SRS)和非手术切除样本(NSRS)之间的差异,本研究收集了1357例经组织病理学诊断为肺癌的手术组织和145例活检样本,以检测EGFR、KRAS、BRAF、EML4-ALK和ROS1的突变状态。

结果

我们收集的两组患者在年龄、性别和组织学类型方面无显著差异;然而,在分期方面存在显著差异。手术组早期患者较多,而非手术组晚期肺癌患者较多。在突变分析中,我们还发现两组之间在所有检测的驱动基因中均无显著差异。

结论

手术切除样本和活检样本均可用于进行驱动基因突变检测。

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Targeted therapy for lung cancer: present and future.肺癌的靶向治疗:现状与未来。
Ann Palliat Med. 2014 Jul;3(3):229-35. doi: 10.3978/j.issn.2224-5820.2014.06.01.
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Lung cancer molecular epidemiology in China: recent trends.中国肺癌分子流行病学:近期趋势。
Transl Lung Cancer Res. 2014 Oct;3(5):270-9. doi: 10.3978/j.issn.2218-6751.2014.09.01.
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ERCC1 and personalized medicine in lung cancer.ERCC1 与肺癌的个体化医学。
Ann Transl Med. 2014 Apr;2(4):32. doi: 10.3978/j.issn.2305-5839.2013.12.01.
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