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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorCanale, Matteo
dc.contributor.authorAngeli, Davide
dc.contributor.authorTedaldi, Gianluca
dc.contributor.authorPriano, Ilaria
dc.contributor.authorUrbini, Milena
dc.contributor.authorPetracci, Elisabetta
dc.date.accessioned2025-04-25T05:57:36Z
dc.date.available2025-04-25T05:57:36Z
dc.date.issued2025-02-20
dc.identifier.citationCanale M, Urbini M, Petracci E, Angeli D, Tedaldi G, Priano I, et al. Genomic Profiling of Extensive Stage Small-Cell Lung Cancer Patients Identifies Molecular Factors Associated with Survival. Lung Cancer Targets Ther. 2025 Feb 20;16:11-23.
dc.identifier.issn1179-2728
dc.identifier.urihttp://hdl.handle.net/11351/12987
dc.descriptionImmunotherapy; Small-cell lung cancer; Tumor mutation burden
dc.description.abstractObjective: Extensive stage Small-Cell Lung Cancer (ES-SCLC) is the most lethal lung cancer, and the addition of immunotherapy conferred a slight survival benefit for patients. Extensive molecular profiling of patients treated with chemotherapy (CT) or chemotherapy plus immunotherapy (CT+IO) would be able to identify molecular factors associated with patients' survival. Material and methods: In this retrospective study, 99 ES-SCLC patients were considered. Of the 79 includible patients, 42 received CT (median age 71 y/o, I-IIIQ: 65-76), and 37 received CT+IO (median age 71 y/o, I-IIIQ 66-75). The FoundationOne CDx assay was performed on patients' tumor tissues. Results: The most mutated genes were TP53 (99%), RB1 (78%), PTEN (23%) and MLL2 (20%), with no significant differences between the treatment groups. As a continuous variable, Tumor Mutation Burden (TMB) had an effect on patients' progression-free survival (PFS) by type of treatment (HR 1.81 (95%, CI: 0.99-3.31) and HR 0.84 (95%, CI: 0.56-1.26) for patients treated with CT and CT+IO, respectively). TMB was also computed and dichotomized using two different cut-offs: considering cut-offs of 10 mut/Mb and >16 mut/Mb, 45 patients (57%) and 68 patients (86.1%) had a low TMB, respectively. A high TMB (cut-off 10 mut/Mb) predicted worse PFS in patients treated with CT (p=0.046); even though not statistically significant, a high TMB (cut-off 16 mut/Mb) predicted a better survival in patients treated with CT+IO. Moreover, at univariate analysis, MLL2 mutations were associated with better prognosis in the overall case series (HRPFS = 0.51, 95% CI: 0.28-0.94), and overall survival (HROS = 0.52, 95% CI: 0.28-0.97). Conclusion: In ES-SCLC, TMB is associated with worse survival in patients treated with CT alone, and with better survival in patients treated with CT+IO, whether considered as a continuous or a dichotomized variable, at different cut-offs. Alterations in epigenetic factors are also associated to better patient prognosis.
dc.language.isoeng
dc.publisherDove Medical Press
dc.relation.ispartofseriesLung Cancer: Targets and Therapy;16
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectAnomalies cromosòmiques
dc.subjectPulmons - Càncer - Tractament
dc.subjectPulmons - Càncer - Aspectes genètics
dc.subjectQuimioteràpia combinada
dc.subjectPulmons - Càncer - Prognosi
dc.subjectMarcadors tumorals
dc.subject.meshMutation
dc.subject.meshSmall Cell Lung Carcinoma
dc.subject.mesh/drug therapy
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshPrognosis
dc.subject.meshBiomarkers, Tumor
dc.titleGenomic Profiling of Extensive Stage Small-Cell Lung Cancer Patients Identifies Molecular Factors Associated with Survival
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.2147/LCTT.S492825
dc.subject.decsmutación
dc.subject.decscarcinoma pulmonar de células pequeñas
dc.subject.decs/farmacoterapia
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decspronóstico
dc.subject.decsmarcadores tumorales
dc.relation.publishversionhttps://doi.org/10.2147/LCTT.S492825
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Canale M, Urbini M, Tedaldi G] Biosciences Laboratory, IRCCS Istituto Romagnolo per Lo Studio Dei Tumori (IRST) “dino Amadori”, Meldola, Italy. [Petracci E, Angeli D] Unit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) “Dino Amadori”, Meldola, Italy. [Priano I] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Servei d’Oncologia Mèdica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid39995768
dc.identifier.wos001429215900001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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