• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1159/000334827
PMID:22286583
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。

相似文献

1
Personalized therapy of lung cancer.肺癌的个性化治疗。
Onkologie. 2012;35 Suppl 1:14-9. doi: 10.1159/000334827. Epub 2012 Jan 20.
2
Recent issues in first-line treatment of advanced non-small-cell lung cancer: Results of an International Expert Panel Meeting of the Italian Association of Thoracic Oncology.晚期非小细胞肺癌一线治疗的最新问题:意大利胸部肿瘤学会国际专家小组会议的结果。
Lung Cancer. 2010 Jun;68(3):319-31. doi: 10.1016/j.lungcan.2009.11.018. Epub 2009 Dec 24.
3
The role of molecular analyses in the diagnosis and treatment of non-small-cell lung carcinomas.分子分析在非小细胞肺癌诊断和治疗中的作用。
Semin Diagn Pathol. 2013 Nov;30(4):298-312. doi: 10.1053/j.semdp.2013.11.007. Epub 2013 Nov 13.
4
Crizotinib, a small-molecule dual inhibitor of the c-Met and ALK receptor tyrosine kinases.克唑替尼,一种c-Met和ALK受体酪氨酸激酶的小分子双重抑制剂。
Curr Opin Investig Drugs. 2010 Dec;11(12):1477-90.
5
Targeting non-small cell lung cancer with epidermal growth factor tyrosine kinase inhibitors: where do we stand, where do we go.表皮生长因子酪氨酸激酶抑制剂靶向治疗非小细胞肺癌:我们目前的状况与未来的方向
Crit Rev Oncol Hematol. 2004 Jun;50(3):175-86. doi: 10.1016/j.critrevonc.2004.02.004.
6
The impact on the multidisciplinary team of molecular profiling for personalized therapy in non-small cell lung cancer.分子谱分析对非小细胞肺癌个体化治疗的多学科团队的影响。
Lung Cancer. 2013 Feb;79(2):101-3. doi: 10.1016/j.lungcan.2012.10.016. Epub 2012 Nov 22.
7
Personalized medicine for non-small-cell lung cancer.非小细胞肺癌的个体化医学。
Expert Rev Anticancer Ther. 2010 Oct;10(10):1601-11. doi: 10.1586/era.10.76.
8
Personalized medicine for lung cancer: new challenges for pathology.肺癌的个体化医学:病理的新挑战。
Histopathology. 2012 Mar;60(4):531-46. doi: 10.1111/j.1365-2559.2011.03854.x. Epub 2011 Sep 14.
9
Biological markers in lung cancer: A clinician's perspective.肺癌的生物学标志物:临床医生的视角。
Cancer Biomark. 2010;6(3-4):123-35. doi: 10.3233/CBM-2009-0124.
10
New targets in advanced NSCLC: EML4-ALK.晚期非小细胞肺癌的新靶点:棘皮动物微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)
Clin Adv Hematol Oncol. 2011 Mar;9(3):207-14.

引用本文的文献

1
Molecular pathological predictive diagnostics in a patient with non-small cell lung cancer treated with crizotinib therapy: A case report.克唑替尼治疗非小细胞肺癌患者的分子病理预测诊断:一例报告
Oncol Lett. 2017 Dec;14(6):7545-7548. doi: 10.3892/ol.2017.7167. Epub 2017 Oct 11.
2
Crizotinib: a review of its use in the treatment of anaplastic lymphoma kinase-positive, advanced non-small cell lung cancer.克唑替尼:治疗间变性淋巴瘤激酶阳性的晚期非小细胞肺癌的应用评价。
Drugs. 2013 Dec;73(18):2031-51. doi: 10.1007/s40265-013-0142-z.
3
FGFR1 expression and gene copy numbers in human lung cancer.
人肺癌中 FGFR1 的表达和基因拷贝数。
Virchows Arch. 2012 Jul;461(1):49-57. doi: 10.1007/s00428-012-1250-y. Epub 2012 May 31.