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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
Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Theme Cancer, Medical Unit Head and Neck, Lung, and Skin Tumors, Thoracic Oncology Center, Karolinska University Hospital, Stockholm, Sweden.
Region Östergötland, Center for Surgery, Orthopaedics and Cancer Treatment, Department of Respiratory Medicine.ORCID iD: 0000-0002-3773-7909
Epistat AB, Uppsala, Sweden.
MSD, Centre for Observational and Real-World Evidence, Stockholm, Sweden.
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2024 (English)In: Acta Oncologica, ISSN 0284-186X, E-ISSN 1651-226X, Vol. 63, p. 198-205Article in journal (Refereed) Published
Abstract [en]

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 regi-men, 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. © 2024 The Author(s).

Place, publisher, year, edition, pages
Medical Journals Sweden AB , 2024. Vol. 63, p. 198-205
Keywords [en]
class of therapy, immunotherapy, non-small cell lung cancer, overall survival, PDL-1 testing, real-world evidence, B7-H1 Antigen, Carcinoma, Non-Small-Cell Lung, Humans, Lung Neoplasms, Retrospective Studies, Sweden, antineoplastic agent, antineoplastic metal complex, programmed death 1 ligand 1, programmed death 1 ligand 1 inhibitor, protein inhibitor, protein tyrosine kinase inhibitor, unclassified drug, vasculotropin inhibitor, advanced cancer, aged, Article, cancer combination chemotherapy, cancer immunotherapy, cancer patient, cancer registry, cancer staging, cohort analysis, controlled study, drug withdrawal, ECOG Performance Status, female, first-line treatment, histology, human, major clinical study, male, monotherapy, non small cell lung cancer, retrospective study, systemic therapy, treatment outcome, unspecified side effect, epidemiology, lung tumor, metabolism
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:liu:diva-211892DOI: 10.2340/1651-226X.2024.20309ISI: 001247319100001Scopus ID: 2-s2.0-85191106137OAI: oai:DiVA.org:liu-211892DiVA, id: diva2:1940451
Available from: 2025-02-26 Created: 2025-02-26 Last updated: 2025-02-26

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