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Current status of vandetanib (ZD6474) in the treatment of non-small cell lung cancer

机译:凡德他尼(ZD6474)在非小细胞肺癌治疗中的现状

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Vandetanib (ZD6474) is an oral small molecule inhibitor of multiple intracellular receptor kinases, including the vascular endothelial growth factor receptor (VEGFR) -2 and epidermal growth factor receptor (EGFR). Both VEGFR and EGFR pathways have emerged as instrumental in the growth and metastasis of multiple malignancies, including non-small cell lung cancer (NSCLC). Indeed, inhibitors of each pathway have been approved by the US Food and Drug Administration for use in advanced NSCLC. As there is considerable cross talk between these pathways, dual inhibition with such agents has become an attractive strategy, with encouraging Phase II clinical trial data to date. The convenience of one oral agent targeting both pathways is clear, and clinical trials have established the maximum tolerated daily dose of vandetanib, with data from randomized Phase III trials emerging. This report will review completed and ongoing NSCLC clinical trials evaluating vandetanib, and speculate on the future of this agent in NSCLC.
机译:Vandetanib(ZD6474)是多种细胞内受体激酶的口服小分子抑制剂,包括血管内皮生长因子受体(VEGFR)-2和表皮生长因子受体(EGFR)。 VEGFR和EGFR通路均已成为包括非小细胞肺癌(NSCLC)在内的多种恶性肿瘤生长和转移的重要工具。实际上,每种途径的抑制剂已被美国食品和药物管理局批准用于晚期NSCLC。由于这些途径之间存在相当大的交叉作用,因此迄今为止,令人鼓舞的II期临床试验数据已证明使用此类药物双重抑制已成为一种有吸引力的策略。靶向两种途径的一种口服药物的便利性显而易见,并且临床试验已经确定了vandetanib的最大每日耐受剂量,并且出现了来自随机III期试验的数据。本报告将回顾评估vandetanib的已完成和正在进行的NSCLC临床试验,并推测该药物在NSCLC中的未来。

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