Department of Urology, Emory University, Atlanta, GA, USA.
Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR, USA.
Adv Exp Med Biol. 2019;1210:121-147. doi: 10.1007/978-3-030-32656-2_7.
Prostate cancer is one of the most common cancers in men and a leading cause of cancer-related death. Recent advances in the treatment of advanced prostate cancer, including the use of more potent and selective inhibitors of the androgen signaling pathway, have provided significant clinical benefit for men with metastatic castration-resistant prostate cancer (mCRPC). However, most patients develop progressive lethal disease, highlighting the need for more effective treatments. One such approach is immunotherapy, which harness the power of the patient's immune system to identify and destroy cancer cells through the activation of cytotoxic CD8 T cells specific for tumor antigens. Although immunotherapy, particularly checkpoint blockade, can induce significant clinical responses in patients with solid tumors or hematological malignancies, minimal efficacy has been observed in men with mCRPC. In the current review, we discuss our current understanding of the immunological complexity of the immunosuppressive prostate cancer microenvironment, preclinical models of prostate cancer, and recent advances in immunotherapy clinical trials to improve outcomes for men with mCRPC.
前列腺癌是男性最常见的癌症之一,也是癌症相关死亡的主要原因。近年来,晚期前列腺癌治疗方面的进展,包括雄激素信号通路更有效和更具选择性的抑制剂的应用,为转移性去势抵抗性前列腺癌(mCRPC)患者提供了显著的临床获益。然而,大多数患者会发展为进行性致命疾病,这凸显了需要更有效的治疗方法。免疫疗法就是一种这样的方法,它利用患者的免疫系统的力量,通过激活针对肿瘤抗原的细胞毒性 CD8 T 细胞来识别和破坏癌细胞。尽管免疫疗法,特别是检查点阻断,在实体瘤或血液恶性肿瘤患者中可以诱导显著的临床反应,但在 mCRPC 男性中观察到的疗效很小。在当前的综述中,我们讨论了我们对免疫抑制性前列腺癌微环境的免疫学复杂性、前列腺癌的临床前模型以及免疫疗法临床试验的最新进展的现有认识,以期改善 mCRPC 男性的治疗效果。