Narayanan Sujata, Srinivas Sandy
Clinical Development, Medivation Inc., San Francisco, CA, USA.
Division of Medical Oncology, Stanford University School of Medicine, 875 Blake Wilbur Drive, Stanford, CA 94305, USA.
Ther Adv Med Oncol. 2017 Jan;9(1):33-45. doi: 10.1177/1758834016667179. Epub 2016 Sep 16.
Patients with relapsed or refractory urothelial carcinoma (UC) have poor prognosis coupled with few options for systemic treatment. The role of angiogenesis in the evolution of cancers has been established, and studies have shown that it plays a key role in the pathogenesis of UC. Many targeted agents have been used in phase I-II trials for the treatment of UC, with encouraging but modest results. Recently, studies combining angiogenesis inhibitors with other chemotherapeutic agents were able to achieve objective responses higher than most commonly used second-line therapies in UC. Future efforts in investigating these therapies in UC rely on identification of biomarkers and other predictors of response to anti-VEGF therapy.
复发或难治性尿路上皮癌(UC)患者预后较差,全身治疗选择有限。血管生成在癌症发展中的作用已得到证实,研究表明其在UC发病机制中起关键作用。许多靶向药物已用于UC治疗的I-II期试验,结果令人鼓舞但效果一般。最近,将血管生成抑制剂与其他化疗药物联合使用的研究能够实现高于UC中最常用二线疗法的客观缓解率。未来在UC中研究这些疗法的工作依赖于生物标志物的识别以及对抗VEGF治疗反应的其他预测指标。