Department of Pulmonology, Kepler University Hospital Krankenhausstrasse 9, 4020 Linz, Austria(1).
Department of Pulmonology, Kepler University Hospital Krankenhausstrasse 9, 4020 Linz, Austria(1).
Lung Cancer. 2019 Aug;134:59-65. doi: 10.1016/j.lungcan.2019.05.033. Epub 2019 May 31.
To evaluate serum tumor markers (STM) as biomarkers for treatment monitoring and prognosis in advanced non-small cell lung cancer (NSCLC) treated with single-agent PD-1/PD-L1-directed immune checkpoint inhibitor (ICI) therapy.
Carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA19-9), cytokeratin-19 fragments (CYFRA 21-1) and neuron specific enolase (NSE) were routinely measured at NSCLC diagnosis, initially elevated markers were used for follow-up. Leading STM change between ICI initiation and first subsequent restaging as well as corresponding computed tomography evaluations according to response evaluation criteria in solid tumors (RECIST) were retrospectively analyzed regarding progression-free (PFS) and overall survival (OS). In uni- and multivariate stepwise Cox-regression analyses, STM and RECIST response were analyzed for their impact on PFS and OS together with other known prognostic patient and tumor characteristics.
Among 84 patients (61% men, mean age 68 years), median PFS was significantly (p < 0.001) longer, when STM decreased (11 M (7,19) N = 37) than in case of increases (<2-fold: 6 M (3,8) N = 31; ≥2-fold: 2 M (1,2) N = 16). Patients with initial STM decrease had longer (p < 0.001) median OS (not reached) than with STM increase (<2-fold: 14 M (12,26); ≥2-fold: 4 M (3,7)). Patients with stable or progressive disease by RECIST and concomitant STM decrease had longer (p < 0.001) PFS and OS (8 M (4,14) and 18 M (10,n.e.) N = 24) than upon STM increase (PFS: 2 M (2,4); OS: 10 M (6,13) N = 42). Significant impact on PFS was shown for STM response (p < 0.001), RECIST response (p = 0.003) and PD-L1 status (p = 0.003). For OS, STM response (p < 0.001), presence of cerebral metastases (p = 0.036) and therapy line ≥3 (p = 0.001) were identified.
Decreasing leading STM at first restaging predict longer PFS and OS and identify patients with favorable outcomes among initial radiological non-responders in ICI treated NSCLC patients.
评估血清肿瘤标志物(STM)作为单药 PD-1/PD-L1 定向免疫检查点抑制剂(ICI)治疗晚期非小细胞肺癌(NSCLC)治疗监测和预后的生物标志物。
在 NSCLC 诊断时常规测量癌胚抗原(CEA)、糖链抗原 19-9(CA19-9)、细胞角蛋白 19 片段(CYFRA 21-1)和神经元特异性烯醇化酶(NSE),最初升高的标志物用于随访。根据实体瘤反应评估标准(RECIST),回顾性分析 ICI 起始和首次后续重新分期之间的主要 STM 变化以及相应的计算机断层扫描评估,以评估无进展生存期(PFS)和总生存期(OS)。在单变量和多变量逐步 Cox 回归分析中,分析 STM 和 RECIST 反应对 PFS 和 OS 的影响,以及其他已知的预后患者和肿瘤特征。
在 84 例患者(61%为男性,平均年龄 68 岁)中,当 STM 下降(11 M(7,19)N = 37)时,PFS 明显(p<0.001)更长,而在增加的情况下(<2 倍:6 M(3,8)N = 31;≥2 倍:2 M(1,2)N = 16)。初始 STM 下降的患者具有更长的(p<0.001)中位 OS(未达到),而 STM 增加的患者则更短(<2 倍:14 M(12,26);≥2 倍:4 M(3,7))。RECIST 稳定或进展且同时伴有 STM 下降的患者(p<0.001)的 PFS 和 OS 更长(8 M(4,14)和 18 M(10,无终点)N = 24),而 STM 增加时(PFS:2 M(2,4);OS:10 M(6,13)N = 42)。STM 反应(p<0.001)、RECIST 反应(p=0.003)和 PD-L1 状态(p=0.003)对 PFS 有显著影响。对于 OS,STM 反应(p<0.001)、脑转移存在(p=0.036)和治疗线数≥3(p=0.001)被确定。
首次重新分期时降低主要 STM 可预测更长的 PFS 和 OS,并可识别出 ICI 治疗 NSCLC 患者中最初影像学无反应者中预后良好的患者。