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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMerino Casabiel, Xavier
dc.contributor.authorVargas-Accarino, Elena
dc.contributor.authorHiguera Urbano, Monica
dc.contributor.authorBermúdez-Ramos, Maria
dc.contributor.authorSoriano, Agnès
dc.contributor.authorTorrens Buscató, Maria
dc.contributor.authorPons, Mònica
dc.contributor.authorRODRIGUEZ-FRIAS, FRANCISCO
dc.contributor.authorMinguez, Beatriz
dc.date.accessioned2025-05-06T10:11:58Z
dc.date.available2025-05-06T10:11:58Z
dc.date.issued2025-03
dc.identifier.citationVargas-Accarino E, Higuera M, Bermúdez-Ramos M, Soriano-Varela A, Torrens M, Pons M, et al. Harnessing Plasma Biomarkers to Predict Immunotherapy Outcomes in Hepatocellular Carcinoma: The Role of cfDNA, ctDNA, and Cytokines. Int J Mol Sci. 2025 Mar;26(6):2794.
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/11351/13037
dc.descriptionBiomarkers; Hepatocellular carcinoma; Immunotherapy
dc.description.abstractImmunotherapy has improved survival in patients with advanced hepatocellular carcinoma (HCC); yet, objective radiological responses occur in only about 20% of cases, suggesting variable benefits. This study aimed to identify serologic markers predictive of response to immune checkpoint inhibitors (ICIs). A cohort of 38 advanced HCC patients receiving immunotherapy was prospectively analyzed. Levels of cell-free DNA (cfDNA), circulating tumor DNA (ctDNA), and cytokines were measured pre-treatment and three months post-treatment initiation. Genomic profiling of ctDNA was also conducted. Baseline levels of cfDNA and ctDNA effectively discriminated HCC patients based on their radiological response to ICIs. Additionally, individuals with pathologic mutations in the CDKN2A gene exhibited significantly reduced survival. Patients with progressive disease (PD) as their best radiological response had significantly fewer copy number variations (CNVs) than those with a radiological response. Furthermore, levels of IL10, PD1, and TGFβ assessed after three months of treatment showed significant variations correlating with survival status. In conclusion, the analysis of cfDNA, ctDNA, and cytokines may improve treatment selection for HCC patients by predicting their expected response to immunotherapies.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesInternational Journal of Molecular Sciences;26(6)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectFetge - Càncer - Immunoteràpia
dc.subjectCitocines
dc.subjectMarcadors tumorals
dc.subjectÀcids nucleics
dc.subject.meshCarcinoma, Hepatocellular
dc.subject.mesh/therapy
dc.subject.meshImmunotherapy
dc.subject.meshLiver Neoplasms
dc.subject.meshCirculating Tumor DNA
dc.subject.meshCell-Free Nucleic Acids
dc.subject.meshCytokines
dc.titleHarnessing Plasma Biomarkers to Predict Immunotherapy Outcomes in Hepatocellular Carcinoma: The Role of cfDNA, ctDNA, and Cytokines
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/ijms26062794
dc.subject.decscarcinoma hepatocelular
dc.subject.decs/terapia
dc.subject.decsinmunoterapia
dc.subject.decsneoplasias hepáticas
dc.subject.decsADN tumoral circulante
dc.subject.decsácidos nucleicos libres de células
dc.subject.decscitocinas
dc.relation.publishversionhttps://doi.org/10.3390/ijms26062794
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Vargas-Accarino E] Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Departament de medicina, Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain. [Higuera M] Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Bermúdez-Ramos M] Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Departament de medicina, Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. [Soriano-Varela A, Torrens M] Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei d’Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Pons M] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. Servei d’Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Rodríguez-Frías F] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. Servei de Microbiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Servei de Bioquímica Clínica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Merino X] Servei de Radiodiagnòstic, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Mínguez B] Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Departament de medicina, Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. Servei d’Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid40141436
dc.identifier.wos001452580200001
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/PI21%2F00714
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/PI18%2F00961
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/FI18%2F00027
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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