School of Medicine, University of Dundee, Dundee, UK.
Tayside Cancer Centre, NHS Tayside, Dundee, UK.
BMJ Open. 2023 Nov 21;13(11):e076715. doi: 10.1136/bmjopen-2023-076715.
Pembrolizumab is a programmed cell death protein-1 (PD-1) inhibitor used to treat advanced patients with non-small cell lung cancer (NSCLC) with a programmed cell death ligand-1 (PD-L1) tumour proportion score (TPS) ≥50. Further sub-division of TPS-based stratification has not been evaluated in the UK, although smoking-induced tumour mutational burden and the immunogenic effects of prior radiotherapy are suggested to improve response.
To investigate if PD-L1 TPS ≥80%, smoking status or radiotherapy before or within 2 months of treatment influenced progression-free survival (PFS) in patients with NSCLC treated with pembrolizumab monotherapy.
PD-L1 TPS, smoking status and radiotherapy exposure were compared in patients with NSCLC in National Health Service (NHS) Tayside (n=100) treated with pembrolizumab monotherapy between 1 November 2017 and 18 February 2022. Survival estimates were compared using log-rank analysis, and Cox proportional hazards analysis was used to investigate the influence of potential confounding factors, including tumour stage and performance status.
PFS was not significantly different (log-rank HR=0.330, p=0.566) comparing patients with PD-L1 TPS 50-79% and PD-L1 TPS ≥80%. Smokers had significantly improved PFS (log-rank HR=4.867, p=0.027), while patients receiving radiotherapy had significantly decreased PFS (log-rank HR=6.649, p=0.012). A Cox regression model confirmed that both radiotherapy (p=0.022) and performance status (p=0.009) were independent negative predictors of PFS.
More rigorous PD-L1 TPS stratification did not influence survival outcomes. Smoking history improved PFS, although it was not an independent response predictor, while radiotherapy and performance status independently influenced clinical response. We suggest that further stratification of PD-L1 TPS is not warranted, while performance status and radiotherapy treatment may be additional clinically useful biomarkers of response to pembrolizumab in patients with NSCLC.
派姆单抗是一种程序性细胞死亡蛋白-1(PD-1)抑制剂,用于治疗 PD-L1 肿瘤比例评分(TPS)≥50%的晚期非小细胞肺癌(NSCLC)患者。尽管吸烟引起的肿瘤突变负担和放疗的免疫原性效应被认为可以提高反应,但在英国尚未对基于 TPS 的分层进行进一步细分。
研究 PD-L1 TPS≥80%、吸烟状态或放疗是否会影响接受派姆单抗单药治疗的 NSCLC 患者的无进展生存期(PFS)。
比较了 2017 年 11 月 1 日至 2022 年 2 月 18 日在苏格兰泰赛德国民保健服务(NHS)接受派姆单抗单药治疗的 NSCLC 患者的 PD-L1 TPS、吸烟状况和放疗暴露情况。采用对数秩分析比较生存估计,采用 Cox 比例风险分析研究潜在混杂因素(包括肿瘤分期和功能状态)的影响。
PD-L1 TPS 为 50-79%和 PD-L1 TPS≥80%的患者 PFS 无显著差异(对数秩 HR=0.330,p=0.566)。吸烟者的 PFS 显著改善(对数秩 HR=4.867,p=0.027),而接受放疗的患者的 PFS 显著降低(对数秩 HR=6.649,p=0.012)。Cox 回归模型证实,放疗(p=0.022)和功能状态(p=0.009)均为 PFS 的独立负预测因子。
更严格的 PD-L1 TPS 分层并未影响生存结果。吸烟史改善了 PFS,但不是独立的反应预测因子,而放疗和功能状态独立影响了临床反应。我们建议,不需要进一步对 PD-L1 TPS 进行分层,而功能状态和放疗治疗可能是 NSCLC 患者对派姆单抗反应的附加临床有用的生物标志物。