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肺癌的个性化治疗。

Personalized therapy of lung cancer.

作者信息

Thomas Roman, Wolf Jürgen

机构信息

Max Planck Institut für Neurologische Forschung, Cologne, Germany.

出版信息

Onkologie. 2012;35 Suppl 1:14-9. doi: 10.1159/000334827. Epub 2012 Jan 20.

Abstract

The implementation of personalized approaches in the treatment of patients with non-small cell lung cancer (NSCLC) requires a precise understanding of tumor biology, a reorientation of clinical development with a strong focus on genetically stratified early phase 'proof of concept' trials, the availability of high-quality 'realtime' genetic diagnostics, and the establishment of networks for molecular screening of lung cancer patients. To achieve this goal, a close interaction between basic researchers, clinical scientists, molecular pathologists, and pharmaceutical companies is essential. We believe that this approach is worth the effort, since personalized therapy in lung cancer has the potential to substantially improve survival in an increasing number of patients. At the moment, established personalized treatment approaches include treatment of patients with NSCLC and activating epidermal growth factor receptor (EGFR) mutations with the EGFR-directed tyrosine kinase inhibitors gefitinib or erlotinib, and treatment of NSCLC patients with genetic aberrations in the anaplastic lymphoma kinase (ALK) oncogene with the mesenchymal-epithelial transition factor (MET)/ALK inhibitor crizotinib. A new approach, the treatment of fibroblast growth factor receptor 1 (FGFR1)-amplified squamous cell lung cancer patients with FGFR inhibitors, is currently being tested in phase I clinical trials.

摘要

在非小细胞肺癌(NSCLC)患者治疗中实施个性化方法,需要精确了解肿瘤生物学,重新定位临床开发方向,重点关注基因分层的早期“概念验证”试验,具备高质量的“实时”基因诊断方法,以及建立肺癌患者分子筛查网络。为实现这一目标,基础研究人员、临床科学家、分子病理学家和制药公司之间的密切互动至关重要。我们认为这种方法值得付出努力,因为肺癌的个性化治疗有可能大幅提高越来越多患者的生存率。目前,已确立的个性化治疗方法包括用表皮生长因子受体(EGFR)靶向酪氨酸激酶抑制剂吉非替尼或厄洛替尼治疗具有EGFR激活突变的NSCLC患者,以及用间充质上皮转化因子(MET)/间变性淋巴瘤激酶(ALK)抑制剂克唑替尼治疗具有ALK致癌基因遗传异常的NSCLC患者。一种新方法,即用FGFR抑制剂治疗成纤维细胞生长因子受体1(FGFR1)扩增的肺鳞状细胞癌患者,目前正在I期临床试验中进行测试。

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