Department of Urology, James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Park 213, Baltimore, MD, 21287, USA.
Department of Oncology, Johns Hopkins University School of Medicine and the Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.
Sci Rep. 2024 Jan 17;14(1):1458. doi: 10.1038/s41598-024-51889-9.
Novel perioperative strategies are needed to reduce recurrence rates in patients undergoing nephrectomy for high-risk, non-metastatic clear cell renal cell carcinoma (ccRCC). We conducted a prospective, phase I trial of neoadjuvant nivolumab prior to nephrectomy in 15 evaluable patients with non-metastatic ccRCC. We leveraged tissue from that cohort to elucidate the effects of PD-1 inhibition on immune cell populations in ccRCC and correlate the evolving immune milieu with anti-PD-1 response. We found that nivolumab durably induces a pro-inflammatory state within the primary tumor, and baseline immune infiltration within the primary tumor correlates with nivolumab responsiveness. Nivolumab increases CTLA-4 expression in the primary tumor, and subsequent nephrectomy increases circulating concentrations of sPD-L1, sPD-L3 (sB7-H3), and s4-1BB. These findings form the basis to consider neoadjuvant immune checkpoint inhibition (ICI) for high-risk ccRCC while the tumor remains in situ and provide the rationale for perioperative strategies of novel ICI combinations.
需要新的围手术期策略来降低接受肾切除术的高危、非转移性透明细胞肾细胞癌 (ccRCC) 患者的复发率。我们在 15 名可评估的非转移性 ccRCC 患者中进行了新辅助纳武单抗治疗肾切除术的前瞻性、I 期试验。我们利用该队列的组织来阐明 PD-1 抑制对 ccRCC 中免疫细胞群的影响,并将不断发展的免疫环境与抗 PD-1 反应相关联。我们发现纳武单抗在原发性肿瘤内持久地诱导促炎状态,并且原发性肿瘤内的基线免疫浸润与纳武单抗的反应性相关。纳武单抗增加原发性肿瘤中的 CTLA-4 表达,随后的肾切除术增加循环中 sPD-L1、sPD-L3 (sB7-H3) 和 s4-1BB 的浓度。这些发现为考虑在肿瘤原位时使用新辅助免疫检查点抑制 (ICI) 治疗高危 ccRCC 提供了基础,并为新型 ICI 联合的围手术期策略提供了依据。