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Concomitant Presence of EGFR and ALK Fusion Gene Mutation in Adenocarcinoma of Lung: A Case Report and Review of the Literature.肺腺癌中EGFR和ALK融合基因突变的同时存在:一例报告并文献复习
J Pharm Pract. 2018 Apr;31(2):244-248. doi: 10.1177/0897190017704751. Epub 2017 Apr 25.
2
Clinical Outcome of ALK-Positive Non-Small Cell Lung Cancer (NSCLC) Patients with De Novo EGFR or KRAS Co-Mutations Receiving Tyrosine Kinase Inhibitors (TKIs).ALK 阳性非小细胞肺癌(NSCLC)患者中初发的 EGFR 或 KRAS 合并突变接受酪氨酸激酶抑制剂(TKI)治疗的临床结局。
J Thorac Oncol. 2017 Apr;12(4):681-688. doi: 10.1016/j.jtho.2016.12.003. Epub 2016 Dec 19.
3
[Lung adenocarcinoma with concomitant EGFR mutation and ALK rearrangement].伴有表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排的肺腺癌
Rev Mal Respir. 2017 May;34(5):576-580. doi: 10.1016/j.rmr.2016.08.002. Epub 2016 Sep 17.
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Clinical outcomes of advanced non-small-cell lung cancer patients with EGFR mutation, ALK rearrangement and EGFR/ALK co-alterations.表皮生长因子受体(EGFR)突变、间变性淋巴瘤激酶(ALK)重排以及EGFR/ALK共同改变的晚期非小细胞肺癌患者的临床结局
Oncotarget. 2016 Oct 4;7(40):65185-65195. doi: 10.18632/oncotarget.11218.
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Concurrent EGFR Mutation and ALK Translocation in Non-Small Cell Lung Cancer.非小细胞肺癌中的表皮生长因子受体(EGFR)突变与间变性淋巴瘤激酶(ALK)易位并存
Cureus. 2016 Feb 26;8(2):e513. doi: 10.7759/cureus.513.
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Adenocarcinoma of the lung with concomitant ALK fusion gene and EGFR gene mutation: A case report and literature review.伴有ALK融合基因及EGFR基因突变的肺腺癌:一例报告并文献复习
Mol Clin Oncol. 2016 Feb;4(2):203-205. doi: 10.3892/mco.2015.684. Epub 2015 Nov 25.
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Cancer statistics in China, 2015.《中国癌症统计数据 2015》
CA Cancer J Clin. 2016 Mar-Apr;66(2):115-32. doi: 10.3322/caac.21338. Epub 2016 Jan 25.
8
Nonsquamous, Non-Small-Cell Lung Cancer Patients Who Carry a Double Mutation of EGFR, EML4-ALK or KRAS: Frequency, Clinical-Pathological Characteristics, and Response to Therapy.携带EGFR、EML4-ALK或KRAS双突变的非鳞状非小细胞肺癌患者:发生率、临床病理特征及对治疗的反应
Clin Lung Cancer. 2016 Sep;17(5):384-390. doi: 10.1016/j.cllc.2015.11.004. Epub 2015 Dec 1.
9
Molecular Epidemiology of EGFR Mutations in Asian Patients with Advanced Non-Small-Cell Lung Cancer of Adenocarcinoma Histology - Mainland China Subset Analysis of the PIONEER study.亚洲腺癌组织学类型晚期非小细胞肺癌患者表皮生长因子受体突变的分子流行病学——中国大陆地区PIONEER研究的亚组分析
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10
Intratumoral Heterogeneity of ALK-Rearranged and ALK/EGFR Coaltered Lung Adenocarcinoma.ALK重排和ALK/EGFR共改变的肺腺癌的肿瘤内异质性
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[非小细胞肺癌中表皮生长因子受体(EGFR)和间变性淋巴瘤激酶(ALK)基因双突变的研究进展]

[Advances in Double Mutations of EGFR and ALK Gene in Non-small Cell Lung Cancer].

作者信息

Wang Xin, Zhong Diansheng

机构信息

Department of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2018 Sep 20;21(9):686-691. doi: 10.3779/j.issn.1009-3419.2018.09.07.

DOI:10.3779/j.issn.1009-3419.2018.09.07
PMID:30201068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6136996/
Abstract

Molecular target therapy is one of the most popular field of non-small cell lung cancer (NSCLC) treatmnet. Epidermal growth factor receptor (EGFR) mutation and anaplastic lymphoma kinase (ALK) rearragement are the most important two oncogenic drivers in NSCLC, early studies suggested that EGFR mutations and ALK rearrangements are mutually exclusive, but isolated cases or small sample research with concomitant EGFR and ALK alterations have been constantly reported. The co-occurrence of EGFR mutations and anaplastic lymphoma kinase (ALK) rearrangements constitutes a rare molecular, the frequency of EGFR/ALK co-alterations was about 1%, however, little has been known about clinicopathologic feature and treatment. This review summarized published case report, EGFR and ALK alterations are common in female, Asian origin, never smoker, IV stage, and denocarcinomas. First-line treatment can choose EGFR or ALK tyrosine kinase inhibitors (TKIs). However, studies about the origin and resistance mechanism in EGFR/ALK co-alterations are little, require more experimental and clinical research.
.

摘要

分子靶向治疗是非小细胞肺癌(NSCLC)治疗中最热门的领域之一。表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排是NSCLC中最重要的两个致癌驱动因素,早期研究表明EGFR突变和ALK重排相互排斥,但不断有关于EGFR和ALK同时改变的孤立病例或小样本研究被报道。EGFR突变和间变性淋巴瘤激酶(ALK)重排同时出现构成一种罕见分子,EGFR/ALK共同改变的频率约为1%,然而,关于其临床病理特征和治疗知之甚少。本综述总结了已发表的病例报告,EGFR和ALK改变在女性、亚洲裔、从不吸烟者、IV期和腺癌中常见。一线治疗可选择EGFR或ALK酪氨酸激酶抑制剂(TKIs)。然而,关于EGFR/ALK共同改变的起源和耐药机制的研究很少,需要更多的实验和临床研究。