Krafft Ulrich, Olah Csilla, Reis Henning, Kesch Claudia, Darr Christopher, Grünwald Viktor, Tschirdewahn Stephan, Hadaschik Boris, Horvath Orsolya, Kenessey Istvan, Nyirady Peter, Varadi Melinda, Modos Orsolya, Csizmarik Anita, Szarvas Tibor
West German Cancer Center, Department of Urology, University of Duisburg-Essen, 45147 Essen, Germany.
Institute of Pathology, University of Duisburg-Essen, 45147 Essen, Germany.
Cancers (Basel). 2021 May 22;13(11):2548. doi: 10.3390/cancers13112548.
Serum PD-L1 (sPD-L1) levels are associated with prognosis in various tumors but has not yet been investigated in advanced bladder cancer. We assessed pretreatment serum samples from 83 BC patients who received platinum chemotherapy and from 12 patients who underwent immune checkpoint inhibitor (ICI) therapy. In addition, on-treatment samples from further therapy cycles were collected during chemotherapy ( = 58) and ICI therapy ( = 11). Serum PD-L1 levels were determined using ELISA. High baseline sPD-L1 levels were associated with worse ECOG status ( = 0.007) and shorter overall survival for both chemotherapy- and ICI-treated patients ( = 0.002 and = 0.040, respectively). Multivariate analysis revealed high baseline sPD-L1 level as an independent predictor of poor survival for platinum-treated patients ( = 0.002). A correlation analysis between serum concentrations of PD-L1 and matrix metalloprotease-7 (MMP-7)-a protease which was recently found to cleave PD-L1-revealed a positive correlation ( = 0.001). No significant sPD-L1 changes were detected during chemotherapy, while in contrast we found a strong, 25-fold increase in sPD-L1 levels during atezolizumab treatment. In conclusion, our work demonstrates that pretreatment sPD-L1 levels are associated with a poor prognosis of BC patients undergoing platinum and ICI therapy. Future research should prospectively address the value of sPD-L1 in predicting treatment response.
血清程序性死亡受体配体1(sPD-L1)水平与多种肿瘤的预后相关,但尚未在晚期膀胱癌中进行研究。我们评估了83例接受铂类化疗的膀胱癌患者以及12例接受免疫检查点抑制剂(ICI)治疗的患者的治疗前血清样本。此外,在化疗(n = 58)和ICI治疗(n = 11)期间收集了后续治疗周期的治疗中样本。使用酶联免疫吸附测定法(ELISA)测定血清PD-L1水平。高基线sPD-L1水平与较差的美国东部肿瘤协作组(ECOG)状态相关(P = 0.007),并且对于接受化疗和ICI治疗的患者,其总生存期均较短(分别为P = 0.002和P = 0.040)。多因素分析显示,高基线sPD-L1水平是铂类治疗患者生存不良的独立预测因素(P = 0.002)。对PD-L1血清浓度与基质金属蛋白酶-7(MMP-7,一种最近发现可裂解PD-L1的蛋白酶)之间的相关性分析显示二者呈正相关(P = 0.001)。化疗期间未检测到sPD-L1有显著变化,而相比之下,我们发现在阿替利珠单抗治疗期间sPD-L1水平有强烈的25倍升高。总之,我们的研究表明,治疗前sPD-L1水平与接受铂类和ICI治疗的膀胱癌患者的不良预后相关。未来的研究应前瞻性地探讨sPD-L1在预测治疗反应中的价值。