Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Urology, Yokohama City University Graduate School of Medicine, 22-2 Seto, Kanazawa Ward, Yokohama, Kanagawa, 236-0027, Japan.
Int J Clin Oncol. 2021 Nov;26(11):2073-2084. doi: 10.1007/s10147-021-01993-x. Epub 2021 Jul 21.
Programmed death-ligand 1 (PD-L1) positivity is associated with poor prognosis in renal cell carcinoma (RCC). Because the prognostic impact and effect of confounding factors are less known, we investigated the prognostic significance of PD-L1 expression in Japanese patients with recurrent/metastatic RCC who started systemic therapy in 2010-2015.
This multicenter, retrospective study recruited patients from 29 Japanese study sites who had prior systemic therapy for RCC (November 2018 to April 2019) and stored formalin-fixed paraffin-embedded primary lesion samples. The primary outcome was overall survival (OS) by PD-L1 expression. Secondary outcomes included OS in subgroups and duration of first- and second-line therapies by PD-L1 expression. OS distributions were estimated using Kaplan-Meier methodology.
PD-L1 expression (on immune cells [IC] ≥ 1%) was observed in 315/770 (40.9%) patients. PD-L1 positivity was more prevalent in patients with poor risk per both Memorial Sloan Kettering Cancer Center [MSKCC] and International Metastatic RCC Database Consortium, and high-risk pathological features (higher clinical stage, nuclear grade and sarcomatoid features). Median OS for PD-L1-positive patients was 30.9 months (95% CI 25.5-35.7) versus 37.5 months (95% CI 34.0-42.6) for PD-L1-negative patients (HR 1.04 [90% CI 0.89-1.22, p = 0.65]; stratified by MSKCC risk and liver metastases). Propensity score weight (PSW)-adjusted OS was similar between PD-L1-positive and -negative patients (median 34.4 versus 31.5 months; estimated PSW-adjusted HR 0.986).
This study suggests PD-L1 status was not an independent prognostic factor in recurrent/metastatic RCC during the study period because PD-L1 positivity was associated with poor prognostic factors, especially MSKCC risk status.
程序性死亡配体 1(PD-L1)阳性与肾细胞癌(RCC)的预后不良相关。由于预后影响和混杂因素的影响知之甚少,我们研究了 PD-L1 表达在 2010-2015 年开始系统治疗的日本复发性/转移性 RCC 患者中的预后意义。
这项多中心、回顾性研究招募了 29 个日本研究点的患者,这些患者先前接受过 RCC 的系统治疗(2018 年 11 月至 2019 年 4 月),并储存了福尔马林固定石蜡包埋的原发病变样本。主要结局是根据 PD-L1 表达评估的总生存期(OS)。次要结局包括根据 PD-L1 表达评估的亚组 OS 和一线和二线治疗的持续时间。使用 Kaplan-Meier 方法估计 OS 分布。
在 770 例患者中,有 315 例(40.9%)观察到 PD-L1 表达(免疫细胞[IC]≥1%)。PD-L1 阳性在 Memorial Sloan Kettering Cancer Center [MSKCC] 和国际转移性 RCC 数据库联盟的风险较高,以及高危病理特征(较高的临床分期、核分级和肉瘤样特征)的患者中更为常见。PD-L1 阳性患者的中位 OS 为 30.9 个月(95%CI 25.5-35.7),PD-L1 阴性患者为 37.5 个月(95%CI 34.0-42.6)(HR 1.04 [90%CI 0.89-1.22,p=0.65];按 MSKCC 风险和肝转移分层)。PD-L1 阳性和阴性患者的倾向评分加权(PSW)调整后的 OS 相似(中位 PSW 调整 HR 0.986)。
本研究表明,在研究期间,PD-L1 状态不是复发性/转移性 RCC 的独立预后因素,因为 PD-L1 阳性与不良预后因素相关,尤其是 MSKCC 风险状况。