Penn State Hershey Cancer Institute, Department of Medicine, Mail Code CH046, 500 University Dr, Hershey, PA 17033, USA.
Curr Mol Pharmacol. 2016;9(3):217-225. doi: 10.2174/1874467208666150716120551.
Prostate cancer was one of the first cancer types where FDA (Food and Drug Administration) approval was granted to a cancer vaccine, sipuleucel-T, in the metastatic setting for asymptomatic or minimally symptomatic patients. This marked the beginning of the era of immunotherapies in cancer and stimulated the interest to develop other immune-based novel agents. In addition to sipuleucel-T vaccine, pox viral-based vaccine and personalized peptide vaccine are also being investigated in prostate cancer. Other agents that modulate the tumor microenvironment to enhance the immune response against the prostate cancer cells is also being developed. Immune checkpoint inhibitors such as ipilimumab, anti-PD-1 monoclonal antibody (programmed cell death-1), and Indoleamine 2,3-dioxygenase (IDO) inhibitors have shown some promise in this field. However, similar to sipuleucel-T vaccine, the preliminary data reflects the efficacy of these to be limited to mCRPC patients with favorable risk factors without any visceral disease. More clinical trials are needed to identify the group of patients with mCRPC that would benefit from immunotherapy. In this article we review the role of immune-based therapies including vaccines and immune checkpoint inhibitors in mCRPC.
前列腺癌是最早获得美国食品和药物管理局(FDA)批准的癌症疫苗之一,即 sipuleucel-T,用于治疗无症状或轻度症状的转移性前列腺癌患者。这标志着癌症免疫治疗时代的开始,并激发了开发其他基于免疫的新型药物的兴趣。除了 sipuleucel-T 疫苗外,痘病毒疫苗和个性化肽疫苗也正在前列腺癌中进行研究。其他能够调节肿瘤微环境以增强针对前列腺癌细胞的免疫反应的药物也在开发中。免疫检查点抑制剂,如 ipilimumab、抗 PD-1 单克隆抗体(程序性细胞死亡蛋白-1)和吲哚胺 2,3-双加氧酶(IDO)抑制剂,在这一领域显示出了一定的前景。然而,与 sipuleucel-T 疫苗类似,初步数据表明,这些药物的疗效仅限于没有内脏疾病且具有有利风险因素的 mCRPC 患者。需要更多的临床试验来确定哪些 mCRPC 患者将从免疫治疗中受益。本文综述了基于免疫的治疗方法,包括疫苗和免疫检查点抑制剂,在 mCRPC 中的作用。