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Lung Cancer. 2015 Dec;90(3):509-15. doi: 10.1016/j.lungcan.2015.10.004. Epub 2015 Oct 9.
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Clin Cancer Res. 2016 Mar 1;22(5):1103-10. doi: 10.1158/1078-0432.CCR-15-1031. Epub 2015 Oct 7.
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N Engl J Med. 2015 Oct 22;373(17):1627-39. doi: 10.1056/NEJMoa1507643. Epub 2015 Sep 27.
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Epidermal Growth Factor Receptor Mutation-Positive Non-Small-Cell Lung Cancer in the Real-World Setting in Central Europe: The INSIGHT Study.表皮生长因子受体突变阳性非小细胞肺癌在中欧真实世界环境中的研究:INSIGHT 研究。
J Thorac Oncol. 2015 Sep;10(9):1370-1374. doi: 10.1097/JTO.0000000000000621.
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The 2015 World Health Organization Classification of Lung Tumors: Impact of Genetic, Clinical and Radiologic Advances Since the 2004 Classification.2015 年世界卫生组织肺肿瘤分类:自 2004 年分类以来遗传、临床和放射学进展的影响。
J Thorac Oncol. 2015 Sep;10(9):1243-1260. doi: 10.1097/JTO.0000000000000630.
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Lancet Oncol. 2015 Aug;16(8):897-907. doi: 10.1016/S1470-2045(15)00006-6. Epub 2015 Jul 5.
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Necitumumab plus gemcitabine and cisplatin versus gemcitabine and cisplatin alone as first-line therapy in patients with stage IV squamous non-small-cell lung cancer (SQUIRE): an open-label, randomised, controlled phase 3 trial.耐昔妥珠单抗联合吉西他滨和顺铂与吉西他滨和顺铂单药一线治疗局部晚期或转移性鳞状非小细胞肺癌患者(SQUIRE):一项开放标签、随机、对照的 3 期临床试验。
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8
EGFR Mutations and Resistance to Irreversible Pyrimidine-Based EGFR Inhibitors.表皮生长因子受体(EGFR)突变与对不可逆嘧啶类EGFR抑制剂的耐药性
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Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M.获得性表皮生长因子受体(EGFR)C797S突变介导携带EGFR T790M的非小细胞肺癌对AZD9291耐药。
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Rociletinib in EGFR-mutated non-small-cell lung cancer.罗西替尼治疗 EGFR 突变型非小细胞肺癌。
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晚期非小细胞肺癌在常规临床实践中的个性化治疗

Personalized treatment of advanced non-small-cell lung cancer in routine clinical practice.

作者信息

Pirker Robert, Filipits Martin

机构信息

Department of Medicine I, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.

出版信息

Cancer Metastasis Rev. 2016 Mar;35(1):141-50. doi: 10.1007/s10555-016-9612-6.

DOI:10.1007/s10555-016-9612-6
PMID:26970967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4821865/
Abstract

Personalized treatment of patients with advanced non-small-cell lung cancer based on clinical and molecular tumor features has entered clinical routine practice. The 2015 pathological classification of lung cancer mandates immunohistochemical and molecular analysis. Therapeutic strategies focused on inhibition of angiogenesis and growth factor receptor signaling. Inhibitors of angiogenesis and monoclonal antibodies directed against the epidermal growth factor receptor have shown efficacy in combination with chemotherapy. Mutations in the epidermal growth factor receptor and anaplastic lymphoma kinase have become clinically relevant therapeutic targets. Immune checkpoint inhibitors are also entering routine clinical practice. Identification of predictive biomarkers is essential and faces several challenges including tumor heterogeneity and dynamic changes of tumor features over time. Liquid biopsies may overcome some of these challenges in the future.

摘要

基于临床和分子肿瘤特征的晚期非小细胞肺癌患者个性化治疗已进入临床常规实践。2015年肺癌病理分类要求进行免疫组织化学和分子分析。治疗策略集中于抑制血管生成和生长因子受体信号传导。血管生成抑制剂和针对表皮生长因子受体的单克隆抗体已显示出与化疗联合使用的疗效。表皮生长因子受体和间变性淋巴瘤激酶的突变已成为具有临床意义的治疗靶点。免疫检查点抑制剂也正在进入常规临床实践。预测性生物标志物的识别至关重要,并且面临包括肿瘤异质性和肿瘤特征随时间动态变化在内的若干挑战。液体活检未来可能会克服其中一些挑战。