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. 2024 Apr 21:63:198-205.
doi: 10.2340/1651-226X.2024.20309.

First-line Treatment Patterns and Outcomes in Advanced Non-Small Cell Lung Cancer in Sweden: A Population-based Real-world Study with Focus on Immunotherapy

Affiliations

First-line Treatment Patterns and Outcomes in Advanced Non-Small Cell Lung Cancer in Sweden: A Population-based Real-world Study with Focus on Immunotherapy

Gunnar Wagenius et al. Acta Oncol. .

Abstract

Background and purpose: The treatment landscape for patients with advanced non-small cell lung cancer (NSCLC) has evolved significantly since the introduction of immunotherapies. We here describe PD-L1 testing rates, treatment patterns, and real-world outcomes for PD-(L)1 inhibitors in Sweden.

Materials and methods: Data were obtained from the Swedish National Lung Cancer Registry for patients with advanced NSCLC and Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2 who initiated first-line -systemic treatment from 01 April 2017 to 30 June 2020. PD-L1 testing was available in the registry from 01 January 2018. Kaplan-Meier was used for overall survival (OS) by type treatment and histology.

Results: A total of 2,204 patients with pathologically confirmed unresectable stage IIIB/C or IV NSCLC initiated first-line treatment, 1,807 (82%) with nonsquamous (NSQ) and 397 (18%) with SQ. Eighty-six per cent (NSQ) or 85% (SQ) had been tested for PD-L1 expression, a proportion that increased over time. The use of platinum-based therapy as first-line treatment decreased substantially over time while there was an upward trend for PD-(L)1-based therapy. Among patients with PS 0-1 initiating a first-line PD-(L)1 inhibitor monotherapy, the median OS was 18.6 and 13.3 months for NSQ and SQ NSCLC patients, respectively, while for the PD-(L)1 inhibitor and chemotherapy combination regimen, the median OS was 24.0 months for NSQ and not evaluable for SQ patients.

Interpretation: The majority of advanced NSCLCs in Sweden were tested for PD-L1 expression. Real-world OS in patients with PS 0-1 receiving first-line PD-(L)1 inhibitor-based regimens was similar to what has been reported in pivotal clinical trials on PD-(L)1 inhibitors.

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Figures

Figure 1
Figure 1
PD-L1 testing by calendar year and by histology.
Figure 2
Figure 2
Distribution of class of therapy by calendar year. (A). Distribution of class of therapy by calendar year (first line, nonsquamous). (B) Distribution of class of therapy by calendar year (first line, squamous).
Figure 3
Figure 3
Overall survival in patients initiating a first-line PD-(L)1 inhibitor-based regimen with ECOG performance status 0–1. (A) Overall survival in PD-(L)1 inhibitor combination in patients with nonsquamous non-small cell lung cancer (NSCLC). (B) Overall survival in PD-(L)1 inhibitor monotherapy in nonsquamous NSCLC. (C) Overall survival in PD-(L)1 inhibitor monotherapy in squamous NSCLC.

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