Department of Urology, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki 036-8203, Japan.
Genes (Basel). 2022 Jul 5;13(7):1204. doi: 10.3390/genes13071204.
Single nucleotide polymorphisms (SNPs) reportedly influence the effect of nivolumab in metastatic renal cell carcinoma (mRCC). This study aimed to evaluate the relationship between the clinical outcomes of patients with mRCC and SNPs in programmed cell death protein 1 (PD-1) protein-coding gene () and explore any potential correlation with patient prognosis and incidence of immune-related adverse events (irAEs). In total, 106 patients with mRCC, who were treated with nivolumab alone ( = 59) or nivolumab and ipilimumab ( = 47), were enrolled in the study. Three SNPs in the gene, namely , , and , were assessed. Patients harboring the allele experienced more severe (odds ratio, 3.390; 95% confidence interval 1.517-7.756; = 0.003) and multiple (OR, 2.778; 95% CI, 1.020-6.993 = 0.031) irAEs than those harboring the genotype. Thus, the existence of the polymorphism ( allele) was associated with the occurrence of severe and multiple irAEs in patients with mRCC. Further evaluation of polymorphisms might help identify patients experiencing irAE by nivolumab treatment.
单核苷酸多态性 (SNP) 据报道会影响纳武利尤单抗治疗转移性肾细胞癌 (mRCC) 的效果。本研究旨在评估 mRCC 患者的临床结局与程序性死亡蛋白 1 (PD-1) 蛋白编码基因 () 中 SNP 之间的关系,并探讨其与患者预后和免疫相关不良事件 (irAE) 发生率的任何潜在相关性。共有 106 例接受纳武利尤单抗单药治疗 (n = 59) 或纳武利尤单抗联合伊匹单抗治疗 (n = 47) 的 mRCC 患者纳入本研究。评估了 基因中的 3 个 SNP,即 、 和 。携带 等位基因的患者发生更严重的 (比值比,3.390;95%置信区间,1.517-7.756;= 0.003) 和多种 (OR,2.778;95%CI,1.020-6.993;= 0.031) irAE 比携带 基因型的患者更严重。因此, 多态性 (等位基因) 的存在与 mRCC 患者发生严重和多种 irAE 有关。进一步评估 多态性可能有助于通过纳武利尤单抗治疗识别发生 irAE 的患者。