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非小细胞肺癌细针穿刺细胞学标本中EGFR和KRAS突变的临床研究

[Clinical Research of EGFR and KRAS Mutation in Fine Needle Aspiration Cytology Specimens of Non-small Cell Lung Carcinoma].

作者信息

Zhang Zhihui, Wu Xilan, Ying Jianming, Li Junling, Qiu Tian, Guo Huiqin, Zhao Huan, Shan Ling, Ling Yun

机构信息

Department of Pathology, Tumor hospital Chinese Academy of Medical Sciences, Beijing 100021, China.

Department of Pathology of Medicine University of Kunming, Kunming 650031, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2015 Apr;18(4):199-205. doi: 10.3779/j.issn.1009-3419.2015.04.05.

DOI:10.3779/j.issn.1009-3419.2015.04.05
PMID:25936883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6000285/
Abstract

BACKGROUND

Epidermal growth factor receptor (EGFR) and KRAS must be detected mutation status before patients of lung cancer use targeted drugs. The aim of this study is to elucidate the significance of EGFR and KRAS mutation in fine needle aspiration (FNA) cytology suspension specimens of non-small cell lung carcinoma.

METHODS

EGFR gene exons 18-21 and KRAS codons 12, 13 of exons 2 were performed by Real-time PCR methods in fine needle aspiration cytology suspension specimens of lymph nodes.

RESULTS

85 metastasis lymph nodes were detected in fine needle aspiration cytology samples of lung cancer. EGFR mutation rate was 37.3%. KRAS mutation rate was 7.2%. 19 formalin fixed paraffin-embedded tissue specimens were available and match cytology specimens. Analysis of EGFR mutation status in those samples revealed agreement with the results obtained in cytological samples (kappa=1.0). Clinical follow-up was available for 13 who presented with stage IV disease. Based on the identification of such mutations, these patients received subsequent therapy with a TKI in clinic. We observed two cases complete remission (16.7%) and 8 cases partial remission (66.7%) and three had ongoing stable disease.

CONCLUSIONS: Fine-needle aspiration cytology samples were detected EGFR and KRAS mutation. The method which collects samples was easier, simple and convenient. This method has higher application value in clinical treatment.
.

摘要

背景

肺癌患者在使用靶向药物前必须检测表皮生长因子受体(EGFR)和KRAS的突变状态。本研究旨在阐明EGFR和KRAS突变在非小细胞肺癌细针穿刺(FNA)细胞学悬液标本中的意义。

方法

采用实时荧光定量PCR方法检测淋巴结细针穿刺细胞学悬液标本中EGFR基因第18-21外显子及KRAS基因第2外显子第12、13密码子。

结果

在肺癌细针穿刺细胞学样本中检测到85个转移淋巴结。EGFR突变率为37.3%。KRAS突变率为7.2%。有19份福尔马林固定石蜡包埋组织标本与细胞学标本匹配。对这些样本中EGFR突变状态的分析显示与细胞学样本结果一致(kappa=1.0)。13例IV期疾病患者有临床随访资料。基于此类突变的鉴定,这些患者在临床上接受了TKI后续治疗。我们观察到2例完全缓解(16.7%),8例部分缓解(66.7%),3例病情持续稳定。

结论

细针穿刺细胞学样本检测到EGFR和KRAS突变。该样本采集方法简便易行。该方法在临床治疗中具有较高的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea22/6000285/8d8c32c36637/zgfazz-18-4-199-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea22/6000285/f387d62ad692/zgfazz-18-4-199-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea22/6000285/8d8c32c36637/zgfazz-18-4-199-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea22/6000285/f387d62ad692/zgfazz-18-4-199-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea22/6000285/8d8c32c36637/zgfazz-18-4-199-2.jpg

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本文引用的文献

1
Detection of EGFR gene mutations in non-small cell lung cancer: lessons from a single-institution routine analysis of 1,403 tumor samples.检测非小细胞肺癌中的 EGFR 基因突变:来自单机构 1403 例肿瘤样本常规分析的经验。
Int J Oncol. 2013 Oct;43(4):1045-51. doi: 10.3892/ijo.2013.2056. Epub 2013 Aug 7.
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Mutations of the EGFR and K-ras genes in resected stage I lung adenocarcinoma and their clinical significance.切除的 I 期肺腺癌中 EGFR 和 K-ras 基因突变及其临床意义。
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Association of epidermal growth factor receptor and K-Ras mutations with smoking history in non-small cell lung cancer patients.
非小细胞肺癌患者中表皮生长因子受体和K-Ras突变与吸烟史的关联
Exp Ther Med. 2013 Feb;5(2):495-498. doi: 10.3892/etm.2012.829. Epub 2012 Nov 23.
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[Relationship of epidermal growth factor receptor gene mutations, clinicopathologic features and prognosis in patients with non-small cell lung cancer].非小细胞肺癌患者表皮生长因子受体基因突变、临床病理特征与预后的关系
Zhonghua Bing Li Xue Za Zhi. 2011 Oct;40(10):679-82.
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Epidermal growth factor receptor and K-Ras in non-small cell lung cancer-molecular pathways involved and targeted therapies.非小细胞肺癌中的表皮生长因子受体和K-Ras——相关分子途径及靶向治疗
World J Clin Oncol. 2011 Nov 10;2(11):367-76. doi: 10.5306/wjco.v2.i11.367.
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Assessment of epidermal growth factor receptor and K-ras mutation status in cytological stained smears of non-small cell lung cancer patients: correlation with clinical outcomes.评估非小细胞肺癌患者细胞学染色涂片的表皮生长因子受体和 K-ras 突变状态:与临床结局的相关性。
Oncologist. 2011;16(6):877-85. doi: 10.1634/theoncologist.2010-0155. Epub 2011 May 14.
7
EGFR and KRAS mutations in lung carcinoma: molecular testing by using cytology specimens.肺癌中 EGFR 和 KRAS 基因突变:细胞学标本的分子检测。
Cancer Cytopathol. 2011 Apr 25;119(2):111-7. doi: 10.1002/cncy.20151. Epub 2011 Mar 11.
8
[Relationship between EGFR and K-ras mutations and clinicopathological characteristics and response to erlotinib treatment in 301 Chinese patients with non-small cell lung cancer].301例中国非小细胞肺癌患者中EGFR与K-ras突变及其与临床病理特征和厄洛替尼治疗反应的关系
Zhonghua Zhong Liu Za Zhi. 2010 Sep;32(9):667-70.
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[EGFR gene mutation status among lung cancer patients in China].[中国肺癌患者的表皮生长因子受体(EGFR)基因突变状态]
Zhonghua Zhong Liu Za Zhi. 2007 Apr;29(4):270-3.
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Distinct epidermal growth factor receptor and KRAS mutation patterns in non-small cell lung cancer patients with different tobacco exposure and clinicopathologic features.不同烟草暴露及临床病理特征的非小细胞肺癌患者中表皮生长因子受体和KRAS的独特突变模式
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