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针对非小细胞肺癌的新型和现有疗法。

Targeting novel and established therapies for non-small cell lung cancer.

作者信息

Spicer James, Chowdhury Simon, Harper Peter

机构信息

Royal Marsden Hospital, Sutton, Surrey SM2 5PT, UK.

出版信息

Cancer Lett. 2007 May 18;250(1):9-16. doi: 10.1016/j.canlet.2006.09.001. Epub 2006 Oct 9.

Abstract

The prognosis in advanced non-small cell cancer (NSCLC) remains poor despite the introduction of several new cytotoxic drugs in the past decade. New approaches are required, and an improved understanding of lung cancer biology is identifying molecular mechanisms that are potential targets for novel therapies. Antagonists of signalling via the erbB and VEGFR families of transmembrane receptors have promising activity in NSCLC, and survival benefit has already been demonstrated for both erlotinib and bevacizumab. Although some patients enjoy dramatic and sustained responses to some of the new targeted drugs, overall response rates in unselected NSCLC patient groups are modest. This reflects the molecular heterogeneity of the disease; further clinical progress will require improved patient selection for treatment with both novel agents and established chemotherapy drugs. Here, we review recent advances in NSCLC biology likely to provide insight into such selection strategies.

摘要

尽管在过去十年中引入了几种新的细胞毒性药物,但晚期非小细胞肺癌(NSCLC)的预后仍然很差。需要新的方法,并且对肺癌生物学的进一步了解正在确定作为新型疗法潜在靶点的分子机制。通过跨膜受体erbB和VEGFR家族进行信号传导的拮抗剂在NSCLC中具有有前景的活性,并且已经证明厄洛替尼和贝伐单抗都能带来生存益处。虽然一些患者对某些新的靶向药物有显著且持续的反应,但在未选择的NSCLC患者群体中总体反应率并不高。这反映了该疾病的分子异质性;进一步的临床进展将需要改进患者选择,以便使用新型药物和已有的化疗药物进行治疗。在此,我们综述了NSCLC生物学的最新进展,这些进展可能为这种选择策略提供见解。

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