Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 10 Center Drive 13N240B, Bethesda, MD, 20892, USA.
Curr Treat Options Oncol. 2018 Mar 8;19(3):16. doi: 10.1007/s11864-018-0523-3.
Bacillus Calmette-Guérin in urothelial carcinoma, high-dose interleukin-2 in renal cell carcinoma, and sipuleucel-T in prostate cancer serve as enduring examples that the host immune response can be harnessed to promote effective anti-tumor immunity in genitourinary malignancies. Recently, cancer immunotherapy with immune checkpoint inhibitors has transformed the prognostic landscape leading to durable responses in a subset of urothelial carcinoma and renal cell carcinoma patients with traditionally poor prognosis. Despite this success, many patients fail to respond to immune checkpoint inhibitors and progression/relapse remains common. Furthermore, modest clinical activity has been observed with ICIs as a monotherapy in advanced PCa. As such, novel treatment approaches are warranted and improved biomarkers for patient selection and treatment response are desperately needed. Future efforts should focus on exploring synergistic and rational combinations that safely and effectively boost response rates and survival in genitourinary malignancies. Specific areas of interest include (1) evaluating the optimal sequencing, disease burden, and timing of immuno-oncology agents with other anti-cancer therapeutics and (2) validating novel biomarkers of response to immunotherapy to optimize patient selection and to identify individuals most likely to benefit from immunotherapy across the heterogenous spectrum of genitourinary malignancies.
卡介苗在尿路上皮癌、高剂量白细胞介素-2 在肾细胞癌和 sipuleucel-T 在前列腺癌中是持久的例子,表明宿主免疫反应可以被利用来促进泌尿生殖系统恶性肿瘤中有效的抗肿瘤免疫。最近,免疫检查点抑制剂的癌症免疫疗法改变了预后情况,导致传统预后不良的一部分尿路上皮癌和肾细胞癌患者出现持久反应。尽管取得了这一成功,但许多患者对免疫检查点抑制剂无反应,进展/复发仍然很常见。此外,ICIs 作为单一药物在晚期 PCa 中的临床活性也很有限。因此,需要新的治疗方法,并迫切需要用于患者选择和治疗反应的改进生物标志物。未来的研究应集中于探索安全有效地提高泌尿生殖系统恶性肿瘤反应率和生存率的协同和合理组合。特别感兴趣的领域包括:(1)评估免疫肿瘤药物与其他抗癌治疗药物的最佳序贯、疾病负担和时机;(2)验证免疫治疗反应的新型生物标志物,以优化患者选择,并确定最有可能从免疫治疗中受益的个体,从而覆盖泌尿生殖系统恶性肿瘤的异质谱。