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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorPiedra, Aida
dc.contributor.authorMartinez-Recio, Sergio
dc.contributor.authorMorán, Teresa
dc.contributor.authorRecuero-Borau, Jordi
dc.contributor.authorHernandez, Ainhoa
dc.contributor.authorArriola, Edurne
dc.contributor.authorCallejo, Ana
dc.contributor.authorIranzo, Patricia
dc.contributor.authorFELIP, ENRIQUETA
dc.date.accessioned2025-02-03T10:38:12Z
dc.date.available2025-02-03T10:38:12Z
dc.date.issued2024-12-17
dc.identifier.citationPiedra 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.issn2234-943X
dc.identifier.urihttps://hdl.handle.net/11351/12514
dc.descriptionImmune check-point inhibitors; Non-small cell lung cancer; Predictive factors
dc.description.abstractIntroduction: 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.isoeng
dc.publisherFrontiers Media
dc.relation.ispartofseriesFrontiers in Oncology;14
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectPulmons - Càncer - Tractament
dc.subjectAnticossos monoclonals - Ús terapèutic
dc.subjectMedicaments antineoplàstics - Ús terapèutic
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.mesh/drug therapy
dc.subject.meshAntibodies, Monoclonal, Humanized
dc.subject.meshAntineoplastic Agents, Immunological
dc.subject.mesh/drug therapy
dc.subject.meshTreatment Outcome
dc.titleFirst-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.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3389/fonc.2024.1510278
dc.subject.decscarcinoma de pulmón de células no pequeñas
dc.subject.decs/farmacoterapia
dc.subject.decsanticuerpos monoclonales humanizados
dc.subject.decsinmunoterapia antineoplásica
dc.subject.decs/farmacoterapia
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttps://doi.org/10.3389/fonc.2024.1510278
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut 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.pmid39741981
dc.identifier.wos001387834700001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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