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Non-Small Cell Lung Cancer beyond Biomarkers: The Evolving Landscape of Clinical Trial Design

机译:生物标志物以外的非小细胞肺癌:临床试验设计的发展趋势

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摘要

The approval of EGFR and ALK directed tyrosine kinase inhibitors materialized the concept of tailoring therapy on the basis of specific biomarkers for treating patients with NSCLC. Research for other biologics, although demonstrating clinical benefit, has been less successful so far for producing biomarkers that predict response. Blocking angiogenesis is the prototype for the agents that belong in the latter group that target specific molecules, yet they are currently approved for relatively unselected groups of patients. In order to meet the goal of personalizing care in the various settings of NSCLC, a wealth of biologics and compounds are currently being tested in clinical trials in different phases of clinical development. In a subset of the relevant studies, a biomarker perspective is appreciated. This review summarizes the clinical rationale of the major ongoing phase II and III NSCLC studies that employ targeting specific molecules with novel agents, as well as innovative strategies, and includes a comparative discussion of the different designs.
机译:EGFR和ALK定向酪氨酸激酶抑制剂的批准使基于治疗非小细胞肺癌患者的特定生物标志物的定制疗法的概念得以实现。对其他生物制剂的研究尽管证明了临床益处,但迄今为止在产生可预测反应的生物标志物方面却不太成功。阻断血管生成是属于靶向特定分子的后一组药物的原型,但目前已批准将其用于相对未选择的患者组。为了达到在NSCLC各种环境中实现个性化护理的目标,目前正在临床开发的不同阶段的临床试验中测试大量的生物制剂和化合物。在相关研究的一个子集中,人们对生物标志物的观点表示赞赏。这篇综述总结了正在进行的主要的II期和III期NSCLC研究的临床原理,这些研究采用了具有新型药物靶向特定分子的药物以及创新策略,并对不同设计进行了比较讨论。

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