Effectiveness of PD-(L)1 inhibitors alone or in combination with platinum-doublet chemotherapy in first-line (1L) non-squamous non-small-cell lung cancer (Nsq-NSCLC) with PD-L1-high expression using real-world data

被引:61
作者
Perol, M. [1 ]
Felip, E. [2 ]
Dafni, U. [3 ,4 ]
Polito, L. [5 ]
Pal, N. [6 ]
Tsourti, Z. [4 ]
Ton, T. G. N. [6 ]
Merritt, D. [7 ]
Morris, S. [7 ]
Stahel, R. [8 ]
Peters, S. [9 ,10 ]
机构
[1] Ctr Leon Berard, Med Oncol, Lyon, France
[2] Vall dHebron Univ Hosp, Vall dHebron Inst Oncol, Barcelona, Spain
[3] Natl & Kapodistrian Univ Athens, Athens, Greece
[4] Frontier Sci Fdn Hellas, Athens, Greece
[5] F Hoffmann La Roche Ltd, Prod Dev Data Sci, Basel, Switzerland
[6] Genentech Inc, Prod Dev Data Sci, San Francisco, CA 94080 USA
[7] F Hoffmann La Roche Ltd, Prod Dev Med Affairs, Basel, Switzerland
[8] European Thorac Oncol Platform ETOP, Coordinating Off, Bern, Switzerland
[9] Ctr Hosp Univ Vaudois CHUV, Lausanne, Switzerland
[10] Univ Lausanne, Lausanne, Switzerland
关键词
non-squamous non-small-cell lung cancer; PD-L1; high; immunotherapy; chemotherapy; retrospective cohort; NIVOLUMAB PLUS IPILIMUMAB; SPECIFIED FINAL ANALYSIS; OPEN-LABEL; PHASE-3; PEMBROLIZUMAB; ATEZOLIZUMAB; DOCETAXEL; SURVIVAL; MULTICENTER;
D O I
10.1016/j.annonc.2022.02.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Anti-programmed cell death protein (death-ligand) 1 [PD-(L)1] therapy alone [cancer immunotherapy (CIT)-mono] or combined with platinum-based chemotherapy (CIT-chemo) is used as the first-line treatment for patients with metastatic non-small-cell lung cancer (NSCLC). Our study compared clinical outcomes with CIT-mono versus CIT-chemo in the specific clinical scenario of non-squamous (Nsq)-NSCLC with a high PD-L1 expression of >50% [tumor proportion score (TPS) or tumor cells (TC)].Methods: This was a retrospective cohort study using a real-world de-identified database. Patients with metastatic NsqNSCLC with high PD-L1 expression initiating first-line CIT-mono or CIT-chemo between 24 October 2016 and 28 February 2019 were followed up until 28 February 2020. We compared overall survival (OS) and real-world progression-free survival (rwPFS) using the KaplaneMeier methodology. Hazard ratios (HRs) were adjusted (aHR) for differences in baseline key prognostic characteristics using the inverse probability of treatment weighting methodology.Results: Patients with PD-L1-high Nsq-NSCLC treated with CIT-mono (n = 351) were older and less often presented with de novo stage IV disease than patients treated with CIT-chemo (n = 169). With a median follow-up of 19.9 months for CIT-chemo versus 23.5 months for CIT-mono, median OS and rwPFS did not differ between the two groups [median OS: CIT-chemo, 21.0 months versus CIT-mono, 22.1 months, aHR = 1.03, 95% confidence interval (CI) 0.77-1.39, P = 0.83; median rwPFS: CIT-chemo, 10.8 months versus CIT-mono, 11.5 months, aHR = 1.04, 95% CI 0.78-1.37, P = 0.81]. CIT-chemo showed significant and meaningful improvement in OS and rwPFS versus CIT-mono only in the never-smoker subgroup, albeit among a small sample of patients (n = 50; OS HR = 0.25, 95% CI 0.070.83, interaction P = 0.02; rwPFS HR = 0.40, 95% CI 0.17-0.95, interaction P = 0.04). Conclusion: Except in the subgroup of never-smoker patients, sparing the chemotherapy in first-line CIT treatment does not appear to impact survival outcomes in Nsq-NSCLC patients with high PD-L1 expression.
引用
收藏
页码:511 / 521
页数:11
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