Department of Surgery, University of Colorado, Aurora, CO.
Department of Surgery, University of Colorado, Aurora, CO; University of Colorado Comprehensive Cancer Center, Aurora, CO.
Urol Oncol. 2014 Jan;32(1):16-22. doi: 10.1016/j.urolonc.2013.09.007.
Bladder cancer is a common cancer worldwide. For patients presenting with muscle-invasive disease, the 5-year survival rate is approximately 50%. Cisplatin-based combination chemotherapy is recommended in the neoadjuvant setting before cystectomy and is also the first line in the metastatic setting. However, the survival benefit of such therapy is modest. The identification of pharmacogenomic biomarkers would enable the rational and personalized treatment of patients by selecting those patients that would benefit most from such therapies sparing others the unnecessary toxicity. Conventional therapies would be recommended for an expected responder, whereas a nonresponder would be considered for alternative therapies selected on the basis of the individual's molecular profile. Although few effective bladder cancer therapies have been introduced in the past 30 years, several targeted therapies against the molecular drivers of bladder cancer appear promising. This review summarizes pharmacogenomic biomarkers that require further investigation or prospective evaluation or both, and publicly available tools for drug discovery and biomarker identification from in vitro data.
膀胱癌是一种常见的全球癌症。对于出现肌层浸润性疾病的患者,5 年生存率约为 50%。在膀胱切除术之前的新辅助治疗中,建议使用基于顺铂的联合化疗,并且也是转移性疾病的一线治疗。然而,这种治疗的生存获益是适度的。鉴定药物基因组生物标志物将通过选择最能从这些治疗中获益的患者,并避免其他患者遭受不必要的毒性,从而实现对患者的合理和个性化治疗。对于预期的反应者,将推荐常规治疗,而对于无反应者,则将根据个体的分子特征选择替代治疗方法。尽管在过去 30 年中引入了几种有效的膀胱癌治疗方法,但针对膀胱癌分子驱动因素的几种靶向治疗方法似乎很有前途。本综述总结了需要进一步研究或前瞻性评估或两者兼有的药物基因组生物标志物,以及用于从体外数据发现药物和鉴定生物标志物的公开工具。