Department of Medical Oncology, University Hospital Basel, Basel.
Institute of Pathology and Medical Genetics, University Hospital Basel, Basel.
ESMO Open. 2023 Aug;8(4):101595. doi: 10.1016/j.esmoop.2023.101595. Epub 2023 Jul 11.
The inclusion of immune checkpoint inhibitors (ICIs) in the treatment of operable stage III non-small-cell lung cancer is becoming a new standard. Programmed death-ligand 1 (PD-L1) protein expression on tumor cells has emerged as the most important biomarker for sensitivity to ICIs targeting the programmed cell death protein 1 (PD-1)-PD-L1 axis. Little is known about the impact of neoadjuvant treatment on PD-L1 expression.
We assessed PD-L1 expression by immunohistochemistry (Ventana SP263 assay) on tumor cells in treatment-naive diagnostic tumor samples and matched lung resections from patients with stage III non-small-cell lung cancer included in the Swiss Group for Clinical Cancer Research (SAKK) trials 16/96, 16/00, 16/01, and 16/14. All patients received neoadjuvant chemotherapy (CT) with cisplatin/docetaxel, either as single modality (CT), with sequential radiotherapy [chemoradiation therapy (CRT)] or with the PD-L1 inhibitor durvalumab (CT + ICI).
Overall, 132 paired tumor samples were analyzed from patients with neoadjuvant CT (n = 69), CRT (n = 33) and CT + ICI (n = 30). For CT and CRT, PD-L1 expression before and after neoadjuvant treatment did not differ significantly (Wilcoxon test, P = 0.94). Likewise, no statistically significant difference was observed between CT and CRT for PD-L1 expression after neoadjuvant treatment (P = 0.97). For CT + ICI, PD-L1 expression before and after neoadjuvant treatment also did not differ significantly (Wilcoxon test, P > 0.99). Event-free survival and overall survival for patients with downregulation or upregulation of PD-L1 expression after neoadjuvant treatment were similar.
In our cohort of patients neoadjuvant treatment did not influence PD-L1 expression, irrespective of the specific neoadjuvant treatment protocol. Dynamic change of PD-L1 expression did not correlate with event-free survival or overall survival.
免疫检查点抑制剂(ICIs)在可手术的 III 期非小细胞肺癌(NSCLC)治疗中的应用正成为新的标准。肿瘤细胞程序性死亡配体 1(PD-L1)蛋白的表达已成为对靶向程序性死亡蛋白 1(PD-1)-PD-L1 轴的 ICI 敏感性的最重要生物标志物。关于新辅助治疗对 PD-L1 表达的影响知之甚少。
我们评估了瑞士临床癌症研究组(SAKK)试验 16/96、16/00、16/01 和 16/14 中纳入的 III 期 NSCLC 患者治疗前诊断性肿瘤样本和匹配的肺切除标本中肿瘤细胞的 PD-L1 表达情况,采用免疫组化法(Ventana SP263 检测法)进行检测。所有患者接受顺铂/多西他赛新辅助化疗(CT),单药治疗(CT)、序贯放化疗(放化疗,CRT)或 PD-L1 抑制剂度伐利尤单抗(CT+ICI)。
共分析了来自新辅助 CT(n=69)、CRT(n=33)和 CT+ICI(n=30)患者的 132 对配对肿瘤样本。对于 CT 和 CRT,新辅助治疗前后 PD-L1 表达无显著差异(Wilcoxon 检验,P=0.94)。同样,新辅助治疗后 PD-L1 表达在 CT 和 CRT 之间也无统计学差异(P=0.97)。对于 CT+ICI,新辅助治疗前后 PD-L1 表达也无显著差异(Wilcoxon 检验,P>0.99)。新辅助治疗后 PD-L1 表达下调或上调的患者的无事件生存和总生存相似。
在我们的患者队列中,新辅助治疗无论新辅助治疗方案如何,均不影响 PD-L1 表达。PD-L1 表达的动态变化与无事件生存或总生存无关。