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Novel molecular targets for the therapy of urothelial carcinoma

机译:新型分子靶标治疗尿路上皮癌

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Introduction: First-line platinum-based combinations are active in locally advanced and metastatic urothelial carcinoma; however, long-term outcomes including disease-specific and overall survival remain suboptimal. In addition, approximately 40 50% of patients with advanced urothelial carcinoma have coexisting medical issues that preclude the use of cisplatin-based therapy. Improvements in our understanding of the molecular mechanisms of urothelial tumorigenesis have led to first-generation clinical trials evaluating novel agents targeting molecular pathways. These are particularly relevant in regard to subpopulations. Novel trial designs warrant consideration to accelerate accrual. Areas covered: In this review, novel molecular targets for the therapy of urothelial carcinoma, as well as recently completed and ongoing clinical trials utilizing novel targeted agents, are discussed. A Medline search with key words, abstracts reported at national conferences on urothelial carcinoma and NCI clinical trial identifiers was used for this review. Expert opinion: Improved understanding of molecular biology has identified a number of new molecular targets, but there is a seeming absence of one dominant molecular driver for urothelial cancer. An adaptive and biomarker-derived strategy may be warranted. Clinical trials utilizing targeted agents are ongoing and results are awaited.
机译:简介:一线铂基组合在局部晚期和转移性尿路上皮癌中很活跃。但是,包括特定疾病和整体生存在内的长期结果仍不理想。此外,大约40 50%的晚期尿路上皮癌患者存在共存的医学问题,无法使用基于顺铂的疗法。我们对尿路上皮肿瘤发生分子机制的了解的改进导致了第一代临床试验评估了靶向分子途径的新型药物。这些与亚群特别相关。新颖的试用设计值得考虑以加快应计。涵盖的领域:在这篇综述中,讨论了用于治疗尿路上皮癌的新型分子靶标,以及最近完成和正在进行的利用新型靶向剂的临床试验。在本次综述中使用了Medline搜索,该搜索使用关键词,在全国性会议上报道的关于尿路上皮癌的摘要和NCI临床试验标识符进行了检索。专家意见:对分子生物学的深入了解已经确定了许多新的分子靶标,但似乎缺乏尿路上皮癌的一种主要分子驱动因子。可能需要采取适应性和生物标志物衍生的策略。使用靶向药物的临床试验正在进行中,尚待结果。

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