Jiang Di Maria, Sridhar Srikala S
Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ontario.
Asia Pac J Clin Oncol. 2018 Nov;14 Suppl 5:24-32. doi: 10.1111/ajco.13059.
Metastatic urothelial cancer (UC) is a lethal disease. Until 2016, cytotoxic chemotherapy with substantial toxicity was the only therapeutic option. In the first-line metastatic setting, cisplatin-based combination chemotherapy remains the standard of care. For cisplatin-ineligible patients, carboplatin-based regimens that are less efficacious are often substituted. In platinum-refractory patients, taxanes and vinflunine are the most commonly used. Recently, treatment options have largely expanded with the development of the immune checkpoint inhibitors (ICIs). Here, we review the rationale, clinical trial data and recent advances in biomarker development in the field of immuno-oncology in this disease site. We will also explore future directions of the field with respect to sequencing and combination strategies.
A comprehensive literature review was performed using Pubmed, clinicaltrials.gov, and conference proceedings from the European Society of Medical Oncology (ESMO) and the American Society of Oncology (ASCO).
ICIs have disease activity in metastatic UC. Five ICIs gained FDA regulatory approval in metastatic UC in patients with platinum-refractory disease. Of these five agents, pembrolizumab has level I evidence based on the KEYNOTE-045 phase III trial showing an overall survival benefit of 3 months over standard chemotherapy. ICIs also play a role in the first-line setting for patients who are cisplatin ineligible. Currently, ICIs are administered to unselected patients as reliable predictive biomarkers are lacking; however, this is a very active area of research. The rapid expansion of ICIs has also led to many upcoming trials, testing ICIs earlier in the disease course and in various combination strategies. Studies on optimal sequencing of therapies are eagerly awaited.
转移性尿路上皮癌(UC)是一种致命疾病。直到2016年,具有严重毒性的细胞毒性化疗是唯一的治疗选择。在一线转移性治疗中,以顺铂为基础的联合化疗仍然是标准治疗方案。对于不符合顺铂治疗条件的患者,通常会采用疗效较差的以卡铂为基础的方案。对于铂类难治性患者,紫杉烷类和长春氟宁是最常用的药物。最近,随着免疫检查点抑制剂(ICI)的发展,治疗选择有了很大扩展。在此,我们综述了该疾病部位免疫肿瘤学领域的理论依据、临床试验数据以及生物标志物开发的最新进展。我们还将探讨该领域在测序和联合策略方面的未来发展方向。
使用PubMed、clinicaltrials.gov以及欧洲医学肿瘤学会(ESMO)和美国肿瘤学会(ASCO)的会议记录进行了全面的文献综述。
ICI在转移性UC中具有疾病活性。五种ICI在铂类难治性疾病患者的转移性UC中获得了美国食品药品监督管理局(FDA)的监管批准。在这五种药物中,帕博利珠单抗有基于KEYNOTE - 045 III期试验的I级证据,显示其总生存期比标准化疗长3个月。ICI在不符合顺铂治疗条件的一线患者中也发挥作用。目前,由于缺乏可靠的预测生物标志物,ICI被应用于未筛选的患者;然而,这是一个非常活跃的研究领域。ICI的迅速扩展也导致了许多即将开展的试验,在疾病进程的早期以及各种联合策略中测试ICI。人们急切期待关于治疗最佳顺序的研究。