Kim Kyu Seo, Sekar Rishi R, Patil Dattatraya, Dimarco Michelle A, Kissick Haydn T, Bilen Mehmet A, Osunkoya Adeboye O, Master Viraj A
School of Medicine, Emory University, Atlanta, GA, United States.
Department of Urology, Emory University, Atlanta, GA, United States.
Oncoimmunology. 2018 Jan 10;7(4):e1413519. doi: 10.1080/2162402X.2017.1413519. eCollection 2018.
Programmed cell death protein 1 (PD-1) immune checkpoint inhibitors have shown activity in patients with advanced renal cell carcinoma (RCC). However, the role of PD-1 expression in tumor-infiltrating lymphocytes (TILs) as a biomarker for poor outcome is not clear. In this study, we evaluated the prognostic value of TIL PD-1 expression in patients with clear cell RCC (ccRCC). 82 patients who underwent nephrectomy for localized or metastatic ccRCC and followed up for at least four years were searched from our database and retrospectively enrolled. Their fixed primary tumor specimens were stained with anti-PD-1 (NAT105). The specimens were classified as negative or positive for PD-1 expression, and the positive specimens were further scored in 10% increments. 37 (45.12%) patients were negative (<1% stained), 26 (31.71%) patients were low (<10 and 10%), and 19 (23.17%) patients were high (20-50%) for PD-1 expression. The prognostic value of TIL PD-1 expression was evaluated by univariate Cox proportional hazards regression on overall and recurrence-free survivals. Higher TIL PD-1 expression was not associated with increased risk of death (P = 0.336) or with increased risk of recurrence (P = 0.572). Higher primary tumor stage was associated with increased risk of recurrence (P = 0.003), and higher Fuhrman nuclear grade was associated with increased risk of death (P <0.001) and with increased risk of recurrence (P <0.001). Our study shows that TIL PD-1 expression by immunohistochemistry (IHC) does not correlate with poor clinical outcome in patients with ccRCC and is inferior to established prognosticating tools.
程序性细胞死亡蛋白1(PD-1)免疫检查点抑制剂已在晚期肾细胞癌(RCC)患者中显示出活性。然而,PD-1在肿瘤浸润淋巴细胞(TILs)中的表达作为预后不良生物标志物的作用尚不清楚。在本研究中,我们评估了TIL PD-1表达在透明细胞RCC(ccRCC)患者中的预后价值。从我们的数据库中检索了82例因局限性或转移性ccRCC接受肾切除术并随访至少四年的患者,并进行回顾性纳入。他们的固定原发性肿瘤标本用抗PD-1(NAT105)染色。标本根据PD-1表达分为阴性或阳性,阳性标本进一步以10%的增量评分。37例(45.12%)患者为阴性(<1%染色),26例(31.71%)患者为低表达(<10%和10%),19例(23.17%)患者为高表达(20%-50%)。通过单因素Cox比例风险回归评估TIL PD-1表达对总生存期和无复发生存期的预后价值。较高的TIL PD-1表达与死亡风险增加(P = 0.336)或复发风险增加(P = 0.572)无关。较高的原发性肿瘤分期与复发风险增加相关(P = 0.003),较高的Fuhrman核分级与死亡风险增加(P <0.001)和复发风险增加(P <0.001)相关。我们的研究表明,免疫组织化学(IHC)检测的TIL PD-1表达与ccRCC患者的不良临床结局无关,且不如既定的预后评估工具。