Abstract 339P
Background
Immune checkpoint inhibitors (ICI) improve overall survival (OS) in non-small cell lung cancer (NSCLC) but the efficacy of first- vs second-line ICI is unknown. We compared the outcomes of advanced NSCLC patients with <50% PD-L1 expression who received first- and second-line ICI.
Methods
This Australian-based retrospective cohort study included advanced NSCLC patients with PD-L1 <50% diagnosed between January 2016 and July 2021. All patients received either first- or second-line ICI. Patients with EGFR, ALK or ROS1 sensitising mutations were excluded. The primary endpoint was OS. Secondary endpoints were progression-free survival (PFS), objective response rate (ORR) and adverse events (AEs). OS and PFS were estimated using Kaplan-Meier methods and Cox proportional-hazards models. Prognostic factors were tested using multivariate analyses.
Results
94 patients were eligible. 59% and 41% received first- and second-line ICI respectively. Baseline characteristics were: 56% PD-L1 <1%, 44% PD-L1 1-49%, 65% non-squamous, 66% male, 49% ECOG 0, 96% current/ex-smokers and 86% de-novo metastatic disease. 93% of those who received first-line ICI had concurrent chemotherapy. After a median follow-up of 14 months, there was no significant difference in OS in patients given first- vs second-line ICI (hazard ratio, HR OS 0.68, 95% CI 0.40-1.18, p = 0.17; median OS 16.0 vs 11.8 months). PFS and ORR were better in patients given first-line ICI (HR PFS 0.48, 95% CI 0.30-0.75, p = 0.01; median PFS 7.4 vs 4.2 months; ORR: 45.5% vs 15.4%). In patients aged 50-59 years, OS favoured first-line ICI (p = 0.009). Treatment-related AEs such as constipation/diarrhoea (55% vs 31%) and nausea/vomiting (42% vs 33%) were higher in first-line ICI. Rate of hospitalisations (56% vs. 51%) and immune-related AEs (24% vs. 28%) were similar in both groups.
Conclusions
In advanced NSCLC patients with <50% PD-L1 expression, there was a trend favouring OS in those who received first-line ICI but not statistically significant. However, PFS and ORR favoured first-line ICI. Higher rates of AEs should warrant caution.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
364P - Tepotinib with an EGFR-tyrosine kinase inhibitor (TKI) in patients with EGFR-mutant MET-amplified NSCLC: A case series
Presenter: Azura Ahmad
Session: Poster viewing 05.
365P - Patterns of progression on first-line osimertinib in patients with EGFR mutation-positive advanced non-small cell lung cancer (NSCLC): A Swiss cohort study
Presenter: Alexandra Schuler
Session: Poster viewing 05.
366P - EGFR amplification is a putative resistance mechanism for NSCLC-LM patients with TKI therapy and is associated with poor outcome
Presenter: Hainan Yang
Session: Poster viewing 05.
367P - High-dose aumolertinib in EGFR-mutant NSCLC patients with brain metastases: Primary data from ACHIEVE
Presenter: Yun Fan
Session: Poster viewing 05.
368P - A special Imaging pattern of bilateral diffuse metastases in advanced lung adenocarcinoma harboring EGFR mutations was associated with a favorable prognosis to EGFR-TKIs
Presenter: Zhen-Bang Gu
Session: Poster viewing 05.
370P - Outcomes in patients with EGFR-mutant locally advanced or metastatic NSCLC co-mutations receiving aumolertinib as first-line treatment: A retrospective study
Presenter: Fang Cun
Session: Poster viewing 05.
371P - Real-world data of first-line treatment with aumolertinib for elderly EGFR+ NSCLC patients
Presenter: Haitao Zhang
Session: Poster viewing 05.
373P - Safety and efficacy of aumolertinib treatment in patients with advanced NSCLC harboring uncommon EGFR mutations: Cohort 2
Presenter: WenFeng Fang
Session: Poster viewing 05.