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检查点抑制剂:治疗尿路上皮膀胱癌的新模式。

Checkpoint inhibitors: the new treatment paradigm for urothelial bladder cancer.

机构信息

Department of Hematology/Oncology, Joan C. Edwards School of Medicine Marshall University, 1600 Medical Center Dr, Huntington, WV, 25701, USA.

Department of Internal Medicine, Joan C. Edwards School of Medicine Marshall University, 1600 Medical Center Dr, Huntington, WV, 25701, USA.

出版信息

Med Oncol. 2017 Sep 1;34(10):170. doi: 10.1007/s12032-017-1029-8.

Abstract

Bladder cancer is the most common malignancy involving the genitourinary system (Siegel et al. in CA Cancer J Clin, 66:7-30, 2016). In the USA, it is the fifth most common cancer and approximately 79,000 new cases will be diagnosed in 2017 (Siegel et al. in CA Cancer J Clin, 66:7-30, 2016). The mortality from bladder cancer is approximately 17,000 deaths each year (Siegel et al. in CA Cancer J Clin, 66:7-30, 2016). The incidence rate for bladder cancer is higher in men compared to women. Risk factors are predominantly related to tobacco smoking, although infection with Schistosoma haematobium is another risk factor in selected populations (Antoni et al. in Eur Urol, 71:96-108, 2017). Cisplatin-based systemic chemotherapy regimens remain the standard of care in both the neoadjuvant and metastatic setting for muscle-invasive bladder cancer (Gupta et al. in Cancer, 9(15):1-14, 2017; Von der Maase et al. in J Clin Oncol, 23:4602-4608, 2005; De Santis et al. in J Clin Oncol, 30:191-199, 2012; Bellmunt et al. in J Clin Oncol, 27: 4454-4461, 2009). There is an estimated overall survival of 9-15 months in metastatic bladder cancer in those who receive the standard of care platinum-based chemotherapy (Von der Maase et al. in J Clin Oncol, 23:4602-4608, 2005; De Santis et al. in J Clin Oncol, 30:191-199, 2012). The median survival, however, is significantly reduced after relapse in patient treated with platinum chemotherapy to less than 7 months (Bellmunt et al. in J Clin Oncol, 27: 4454-4461, 2009). Thus, this approach is preferred for patients who can tolerate this treatment as first-line chemotherapy (Gupta et al. in Cancer, 9(15):1-14, 2017). Until recently, there were few treatment options for those patients with poor performance status who are ineligible to receive cisplatin including renal insufficiency and multiple comorbidities or had disease progression after receiving platinum-based chemotherapy (Gupta et al. in Cancer, 9(15):1-14, 2017). With further understanding of tumor immune evasion, systemic immunotherapy which utilizes the patient's own immune system directly to eradicate and target neoplastic cells, has now been approved for urothelial bladder cancer. Monoclonal antibodies that target programmed cell death protein 1 (PD-1), including Nivolumab and Pembrolizumab, and its ligand, PD-L1, including Atezolizumab, Durvalumab, Avelumab, have all been investigated and approved in the setting of metastatic refractory urothelial cancer (Gupta et al. in Cancer, 9(15):1-14, 2017; Von der Maase et al. in J Clin Oncol, 23:4602-4608, 2005; Zilchi et al. in BioMed Res Int, 2017, 2017, doi: 10.1155/2017/5618174 ). Atezolizumab and Pembrolizumab have also been approved as first-line therapy in the setting of cisplatin-ineligible metastatic bladder cancer (Gupta et al. in Cancer, 9(15):1-14, 2017; Zilchi et al. in BioMed Res Int, 2017, 2017, doi: 10.1155/2017/5618174 ). Those that target cytotoxic T-lymphocyte-associated protein 4, including Ipilimumab and Tremelimumab, have also been investigated and further studies are being performed (Gupta et al. in Cancer, 9(15):1-14, 2017; Zilchi et al. in BioMed Res Int, 2017, 2017, doi: 10.1155/2017/5618174 ). This review outlines the systemic immunotherapies that have been approved or are currently being investigated.

摘要

膀胱癌是最常见的涉及泌尿系统的恶性肿瘤(Siegel 等人,CA Cancer J Clin,66:7-30,2016)。在美国,它是第五种最常见的癌症,2017 年预计将诊断出约 79,000 例新病例(Siegel 等人,CA Cancer J Clin,66:7-30,2016)。膀胱癌的死亡率约为每年 17,000 人(Siegel 等人,CA Cancer J Clin,66:7-30,2016)。与女性相比,膀胱癌在男性中的发病率更高。危险因素主要与吸烟有关,尽管在某些人群中,感染血吸虫是另一个危险因素(Antoni 等人,Eur Urol,71:96-108,2017)。顺铂为基础的系统化疗方案仍然是肌层浸润性膀胱癌新辅助和转移性治疗的标准治疗方法(Gupta 等人,Cancer,9(15):1-14,2017;Von der Maase 等人,J Clin Oncol,23:4602-4608,2005;De Santis 等人,J Clin Oncol,30:191-199,2012;Bellmunt 等人,J Clin Oncol,27:4454-4461,2009)。在接受标准铂类化疗的转移性膀胱癌患者中,估计总体生存率为 9-15 个月(Von der Maase 等人,J Clin Oncol,23:4602-4608,2005;De Santis 等人,J Clin Oncol,30:191-199,2012)。然而,在接受铂类化疗治疗后复发的患者中,中位生存期显著缩短,不到 7 个月(Bellmunt 等人,J Clin Oncol,27:4454-4461,2009)。因此,对于能够耐受这种治疗作为一线化疗的患者,这种方法是首选(Gupta 等人,Cancer,9(15):1-14,2017)。直到最近,对于那些身体状况不佳、不能接受顺铂治疗的患者,包括肾功能不全和多种合并症,或在接受铂类化疗后疾病进展的患者,几乎没有治疗选择(Gupta 等人,Cancer,9(15):1-14,2017)。随着对肿瘤免疫逃逸的进一步了解,利用患者自身免疫系统直接消灭和靶向肿瘤细胞的全身性免疫疗法,现已被批准用于膀胱癌。针对程序性死亡蛋白 1(PD-1)的单克隆抗体,包括 Nivolumab 和 Pembrolizumab,以及其配体 PD-L1,包括 Atezolizumab、Durvalumab、Avelumab,都已在转移性复发性尿路上皮癌的治疗中进行了研究和批准(Gupta 等人,Cancer,9(15):1-14,2017;Von der Maase 等人,J Clin Oncol,23:4602-4608,2005;Zilchi 等人,BioMed Res Int,2017,2017,doi: 10.1155/2017/5618174)。Atezolizumab 和 Pembrolizumab 也已被批准用于顺铂不适用的转移性膀胱癌的一线治疗(Gupta 等人,Cancer,9(15):1-14,2017;Zilchi 等人,BioMed Res Int,2017,2017,doi: 10.1155/2017/5618174)。针对细胞毒性 T 淋巴细胞相关蛋白 4 的药物,包括 Ipilimumab 和 Tremelimumab,也进行了研究,目前正在进行进一步的研究(Gupta 等人,Cancer,9(15):1-14,2017;Zilchi 等人,BioMed Res Int,2017,2017,doi: 10.1155/2017/5618174)。本综述概述了已批准或正在研究的系统免疫疗法。

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