| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Piedra, Aida |
| dc.contributor.author | Martinez-Recio, Sergio |
| dc.contributor.author | Morán, Teresa |
| dc.contributor.author | Recuero-Borau, Jordi |
| dc.contributor.author | Hernandez, Ainhoa |
| dc.contributor.author | Arriola, Edurne |
| dc.contributor.author | Callejo, Ana |
| dc.contributor.author | Iranzo, Patricia |
| dc.contributor.author | FELIP, ENRIQUETA |
| dc.date.accessioned | 2025-02-03T10:38:12Z |
| dc.date.available | 2025-02-03T10:38:12Z |
| dc.date.issued | 2024-12-17 |
| dc.identifier.citation | Piedra A, Martínez-Recio S, Hernández A, Morán T, Arriola E, Recuero-Borau J, et al. First-line pembrolizumab in patients with advanced non-small cell lung cancer and high PD-L1 expression: real-world data from a Spanish multicenter study. Front Oncol. 2024 Dec 17;14:1510278. |
| dc.identifier.issn | 2234-943X |
| dc.identifier.uri | https://hdl.handle.net/11351/12514 |
| dc.description | Immune check-point inhibitors; Non-small cell lung cancer; Predictive factors |
| dc.description.abstract | Introduction: Pembrolizumab stands as a first-line option for patients with advanced non-small cell lung cancer (NSCLC) and high programmed death-ligand 1 (PD-L1) expression (PD-L1 ≥50%). Several factors such as antibiotic exposure, low body mass index (BMI), certain metastatic location or poor performance status may influence outcomes.
Methods: We conducted a multicenter retrospective analysis in a cohort of patients with advanced high PD-L1 expression NSCLC treated with first-line pembrolizumab in clinical practice. We sought to evaluate clinical outcomes according to several factors.
Results: Among the 494 included patients, median age was 67.29 years, 77% were male, 54% and 38% were former or current smokers, respectively; 84% had an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0-1, and 48% had a BMI of <25. 32% of patients had bone metastases, 32% brain metastases and 16% liver metastases. 35% of patients had exposure to antibiotics (AB), 44% to corticosteroids and 62% to proton pump inhibitors (PPi). With a median follow-up of 14.3 months, the median overall survival (OS) and progression-free survival (PFS) were 15.9m (95% CI 13.1 to 18.8) and 9.9m (95% CI 7.7 to 12.1), and the overall response rate (ORR) was 43%. After univariate analysis, median OS in patients with ECOG-PS 0 vs. 1 vs. 2 was 36.7m vs. 14.8m vs. 2.7m (p<0.001). Median OS in patients who received treatment with corticosteroids vs. patients without exposure was 11.4m vs. 22.3m (p<0.001). After multivariate analysis, corticosteroid exposure (HR 1.41) and ECOG-PS (HR 2.40) maintained a prognostic impact.
Discussion: First-line pembrolizumab outcomes in advanced high PD-L1 expression NSCLC patients could be negatively influenced by corticosteroid exposure or poor ECOG-PS. |
| dc.language.iso | eng |
| dc.publisher | Frontiers Media |
| dc.relation.ispartofseries | Frontiers in Oncology;14 |
| dc.rights | Attribution 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
| dc.source | Scientia |
| dc.subject | Avaluació de resultats (Assistència sanitària) |
| dc.subject | Pulmons - Càncer - Tractament |
| dc.subject | Anticossos monoclonals - Ús terapèutic |
| dc.subject | Medicaments antineoplàstics - Ús terapèutic |
| dc.subject.mesh | Carcinoma, Non-Small-Cell Lung |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Antibodies, Monoclonal, Humanized |
| dc.subject.mesh | Antineoplastic Agents, Immunological |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Treatment Outcome |
| dc.title | First-line pembrolizumab in patients with advanced non-small cell lung cancer and high PD-L1 expression: real-world data from a Spanish multicenter study |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.3389/fonc.2024.1510278 |
| dc.subject.decs | carcinoma de pulmón de células no pequeñas |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | anticuerpos monoclonales humanizados |
| dc.subject.decs | inmunoterapia antineoplásica |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | resultado del tratamiento |
| dc.relation.publishversion | https://doi.org/10.3389/fonc.2024.1510278 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Piedra A] Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. Department of Medicine, Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain. [Martínez-Recio S] Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. [Hernández A, Morán T] Medical Oncology Department, ICO Badalona, Hospital Universitari Germans Trias i Pujol, Badalona, Spain. [Arriola E, Recuero-Borau J] Medical Oncology Department, Hospital del Mar – Centro de Investigación Biomédica en Red - Cáncer (CIBERONC), Barcelona, Spain. [Callejo A, Iranzo P, Felip E] Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain |
| dc.identifier.pmid | 39741981 |
| dc.identifier.wos | 001387834700001 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |