Department of Nephrology, Chang Gung Memorial Hospital, College of Medicine, Chang Gung University, Taoyuan 33305, Taiwan.
Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Int J Mol Sci. 2020 Nov 26;21(23):8993. doi: 10.3390/ijms21238993.
For a long time, cisplatin-based chemotherapy had been viewed as first-line chemotherapy for advanced and metastatic urothelial carcinoma (UC). However, many patients with UC had been classified as cisplatin-ineligible who can only receive alternative chemotherapy with poor treatment response, and the vast majority of the cisplatin-eligible patients eventually progressed, even those with objective response with cisplatin-based chemotherapy initially. By understanding tumor immunology in UC, immune checkpoint inhibitors, targeting on programmed death 1 (PD-1) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) pathways, had been proven as first-line treatment for cisplatin-ineligible metastatic UC and as second-line treatment for patients with platinum-refractory metastatic UC by the U.S Food and Drug Administration (FDA). In 2020, JAVEIN bladder 100 further reported that PD-L1 inhibitors showed benefits on prolonged survival and progression-free survival as maintenance therapy. Besides targeting on immune checkpoint, manipulation of the tumor microenvironment by metabolic pathways intervention, including inhibition on tumor glycolysis, lactate accumulation and exogenous glutamine uptake, had been investigated in the past few years. In this comprehensive review, we start by introducing traditional chemotherapy of UC, and then we summarize current evidences supporting the use of immune checkpoint inhibitors and highlight ongoing clinical trials. Lastly, we reviewed the tumor metabolic characteristic and the anti-tumor treatments targeting on metabolic pathways.
在很长一段时间里,顺铂为基础的化疗被视为晚期和转移性尿路上皮癌(UC)的一线化疗方案。然而,许多 UC 患者被归类为不适合顺铂治疗的患者,他们只能接受替代化疗,但治疗反应不佳,绝大多数适合顺铂治疗的患者最终还是会进展,即使那些最初对顺铂为基础的化疗有客观反应的患者也是如此。通过了解 UC 中的肿瘤免疫学,美国食品和药物管理局(FDA)已证实,免疫检查点抑制剂,针对程序性死亡 1(PD-1)和细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)途径的药物,可作为不适合顺铂治疗的转移性 UC 的一线治疗方法,以及对铂类耐药的转移性 UC 患者的二线治疗方法。2020 年,JAVEIN bladder 100 进一步报告称,PD-L1 抑制剂作为维持治疗可延长生存和无进展生存期。除了针对免疫检查点外,过去几年还研究了通过代谢途径干预来操纵肿瘤微环境,包括抑制肿瘤糖酵解、乳酸积累和外源性谷氨酰胺摄取。在这篇全面的综述中,我们首先介绍 UC 的传统化疗,然后总结目前支持使用免疫检查点抑制剂的证据,并重点介绍正在进行的临床试验。最后,我们回顾了肿瘤代谢特征和针对代谢途径的抗肿瘤治疗。