Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands.
Department of Genitourinary Medical Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, USA.
Nat Rev Urol. 2024 Jan;21(1):22-34. doi: 10.1038/s41585-023-00801-7. Epub 2023 Aug 22.
Anti-PD1 and anti-PDL1 monotherapies have shown clinical efficacy in stage IV urothelial cancer and are integrated into current clinical practice. However, only a small number of the patients treated with single-agent checkpoint blockade experience an antitumour response. Insufficient priming or inhibitory factors in the tumour immune microenvironment might have a role in the lack of response. CTLA4 is an inhibitory checkpoint on activated T cells that is being studied as a therapeutic target in combination with anti-PD1 or anti-PDL1 therapies in advanced urothelial cancer. In locally advanced urothelial cancer, this combination approach has shown encouraging antitumour effects when administered pre-operatively. We believe that the presence of pre-existing intratumoural T cell immunity is not a prerequisite for response to combination therapy and that the additional value of CTLA4 blockade might involve the broadening of peripheral T cell priming, thereby transforming immunologically cold tumours into hot tumours.
抗 PD1 和抗 PDL1 的单药治疗在 IV 期膀胱癌中显示出了临床疗效,并且已纳入当前的临床实践中。然而,在接受单药检查点阻断治疗的患者中,只有少数人出现抗肿瘤反应。肿瘤免疫微环境中初始激活或抑制因子不足可能在缺乏反应中起作用。CTLA4 是激活的 T 细胞上的一种抑制性检查点,作为一种治疗靶点,正在与晚期膀胱癌中的抗 PD1 或抗 PDL1 治疗联合进行研究。在局部晚期膀胱癌中,该联合治疗方法在术前给药时显示出了令人鼓舞的抗肿瘤效果。我们认为,肿瘤内 T 细胞免疫的预先存在不是对联合治疗反应的先决条件,CTLA4 阻断的额外价值可能涉及外周 T 细胞初始激活的扩大,从而将免疫冷肿瘤转化为热肿瘤。