Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.
JAMA Netw Open. 2023 Jul 3;6(7):e2322915. doi: 10.1001/jamanetworkopen.2023.22915.
Immune checkpoint inhibitor (ICI) monotherapy with pembrolizumab and ICI plus chemotherapy have been approved as first-line treatments for non-small cell lung cancer (NSCLC) for patients with a programmed cell death ligand-1 (PD-L1) tumor proportion score (TPS) of 50% or more, but the choice between these 2 therapeutic options is unclear.
To clarify the association of a history of concurrent medication use with treatment outcomes for ICIs with or without chemotherapy in patients with NSCLC with a high PD-L1 TPS and to determine whether these clinical histories are biomarkers for appropriate treatment selection.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective, multicenter cohort study at 13 hospitals in Japan included patients with advanced NSCLC with a PD-L1 TPS of 50% or more who had received pembrolizumab ICI monotherapy or ICI plus chemotherapy as the initial treatment between March 2017 and December 2020. The median (IQR) follow-up duration was 18.5 (9.2-31.2) months. Data were analyzed from April 2022 through May 2023.
ICI monotherapy with pembrolizumab or ICI plus chemotherapy as first-line treatment.
The primary analysis was the association of treatment outcomes with baseline patient characteristics, including concomitant drug history, after propensity score matching. Cox proportional hazard models were used to determine the associations of patient characteristics with survival outcomes. Logistic regression analysis was used to determine the association of concomitant medication history with treatment outcomes and other patient characteristics.
A total of 425 patients with NSCLC were enrolled in the study including 271 patients (median [range] age, 72 [43-90] years; 215 [79%] men) who were treated with pembrolizumab monotherapy as the first-line treatment and 154 patients (median [range] age, 69 [36-86] years; 121 [79%] men) who were treated with ICI plus chemotherapy as the first-line treatment. In multivariable analysis, a history of proton pump inhibitor (PPI) use was independently associated with shorter progression-free survival (PFS) in the pembrolizumab monotherapy group (hazard ratio [HR], 1.38; 95% CI, 1.00-1.91; P = .048), but not in the ICI plus chemotherapy group. In patients with a PPI history, both the median (IQR) PFS (19.3 [9.0 to not reached] months vs 5.7 [2.4 to 15.2] months; HR, 0.38; 95% CI, 0.20-0.72; P = .002) and the median (IQR) overall survival (not reached [9.0 months to not reached) vs 18.4 [10.5 to 50.0] months; HR, 0.43; 95% CI, 0.20-0.92; P = .03) were significantly longer in the ICI plus chemotherapy group than in the pembrolizumab monotherapy group. In patients without a history of PPI use, both the median (IQR) PFS (18.8 months [6.6 months to not reached] vs 10.6 months [2.7 months to not reached]; HR, 0.81; 95% CI, 0.56-1.17; P = .26) and the median (IQR) overall survival (not reached [12.6 months to not reached] vs 29.9 [13.3 to 54.3] months, HR, 0.75; 95% CI, 0.48-1.18; P = .21) did not differ between groups.
This cohort study found that a history of PPI use could be an important clinical factor in treatment decision-making for patients with NSCLC with a PD-L1 TPS of 50% or more.
对于程序性死亡配体 1(PD-L1)肿瘤比例评分(TPS)为 50%或更高的非小细胞肺癌(NSCLC)患者,免疫检查点抑制剂(ICI)单药治疗联合 ICI 加化疗已被批准为一线治疗方法,但这两种治疗选择之间的选择尚不清楚。
明确同时使用药物治疗与 NSCLC 患者 PD-L1 TPS 高的患者接受 ICI 单药治疗或 ICI 加化疗的治疗结果之间的关联,并确定这些临床病史是否是适当治疗选择的生物标志物。
设计、地点和参与者:这项在日本 13 家医院进行的回顾性多中心队列研究纳入了 2017 年 3 月至 2020 年 12 月期间接受 pembrolizumab ICI 单药治疗或 ICI 加化疗作为初始治疗的 PD-L1 TPS 为 50%或更高的晚期 NSCLC 患者。中位(IQR)随访时间为 18.5(9.2-31.2)个月。数据于 2022 年 4 月至 2023 年 5 月进行分析。
ICI 单药治疗联合 pembrolizumab 或 ICI 加化疗作为一线治疗。
主要分析是在倾向评分匹配后,根据基线患者特征(包括同时使用药物的病史)与治疗结果的相关性。使用 Cox 比例风险模型确定患者特征与生存结果的关联。使用逻辑回归分析确定同时使用药物史与治疗结果和其他患者特征的相关性。
共有 425 名 NSCLC 患者入组本研究,包括 271 名患者(中位[范围]年龄,72[43-90]岁;215[79%]男性)接受 pembrolizumab 单药治疗作为一线治疗,以及 154 名患者(中位[范围]年龄,69[36-86]岁;121[79%]男性)接受 ICI 加化疗作为一线治疗。多变量分析显示,质子泵抑制剂(PPI)的使用史与 pembrolizumab 单药治疗组的无进展生存期(PFS)较短独立相关(风险比[HR],1.38;95%CI,1.00-1.91;P=0.048),但与 ICI 加化疗组无关。在有 PPI 史的患者中,PFS 的中位(IQR)(19.3[9.0 至无进展]个月 vs 5.7[2.4 至 15.2]个月;HR,0.38;95%CI,0.20-0.72;P=0.002)和中位(IQR)总生存期(未达到[9.0 个月至未达到)vs 18.4[10.5 至 50.0]个月;HR,0.43;95%CI,0.20-0.92;P=0.03)在 ICI 加化疗组明显长于 pembrolizumab 单药治疗组。在没有 PPI 史的患者中,PFS 的中位(IQR)(18.8 个月[6.6 个月至无进展] vs 10.6 个月[2.7 个月至无进展];HR,0.81;95%CI,0.56-1.17;P=0.26)和中位(IQR)总生存期(未达到[12.6 个月至未达到)vs 29.9[13.3 至 54.3]个月;HR,0.75;95%CI,0.48-1.18;P=0.21)在两组之间无差异。
这项队列研究发现,质子泵抑制剂(PPI)的使用史可能是 PD-L1 TPS 为 50%或更高的 NSCLC 患者治疗决策中的一个重要临床因素。