Distinct protein and metabolic profiles in patients with advanced clear-cell renal cell carcinoma treated with sunitinib: a study of the Spanish oncology genitourinary group

dc.contributor.authorQuintás, Guillermo
dc.contributor.authorSanmartín, Elena
dc.contributor.authorGarcia Gimenez, Alicia
dc.contributor.authorMuñoz Langa, José
dc.contributor.authorCollado, Aida
dc.contributor.authorSuárez, Cristina
dc.contributor.authorGarcía del Muro Solans, Xavier
dc.contributor.authorMéndez-Vidal, María José
dc.contributor.authorGarcía-Sánchez, José
dc.contributor.authorSalvador Coloma, Carmen
dc.contributor.authorLainez, Nuria
dc.contributor.authorGallardo, Enrique
dc.contributor.authorMunárriz, Javier
dc.contributor.authorVázquez, Sergio
dc.contributor.authorMolins, Carmen
dc.contributor.authorFont de Mora, Jaime
dc.contributor.authorReynes, Gaspar
dc.date.accessioned2026-06-30T16:08:53Z
dc.date.available2026-06-30T16:08:53Z
dc.date.issued2026-04-29
dc.date.updated2026-06-30T16:08:57Z
dc.description.abstractBackground: New biomarkers are needed to improve treatment selection in patients with metastatic clear cell renal cell carcinoma (CCRCC). This study aims to identify predictive biomarkers through the investigation of serum proteins related to angiogenesis and tumor immune escape, alongside metabolic patterns associated with clinical outcomes. Methods: We conducted a prospective, multicenter study in patients with locally advanced or metastatic CCRCC receiving first-line sunitinib. Serum protein levels, including those related to angiogenesis and immune escape, were measured. Additionally, untargeted lipidomic and targeted metabolic analyses focused on tryptophan metabolism and amino acid profiles were performed. Routine blood test results were recorded, and correlations among all parameters were analyzed. Results: Thirty-eight patients from ten Spanish hospitals were included. Median progression-free survival (PFS) was 9.87 months, and median overall survival (OS) was 21.10 months. Multivariate analysis identified higher interleukin-6 (IL-6), arginase-1, and S100 calcium binding protein A9 (S100A9) concentrations as significant predictors of shorter OS. We defined three distinct risk groups based on the combined levels of S100A9 and IL-6: high levels of both proteins, high levels of either one protein, or low levels of both proteins confer a poor, intermediate and favorable prognosis, respectively. Metabolomic analysis revealed significant differences in the tryptophan-kynurenine pathway between patients with extreme PFS and OS phenotypes. Elevated levels of tryptophan metabolites were associated with poorer PFS, while alterations in amino acids and tryptophan metabolites correlated with OS extremes. Notably, significant correlations were observed between IL-6 levels and increased tryptophan metabolism. Conclusions: This study underscores the prognostic value of specific proteins and metabolites in metastatic CCRCC, proposing potential biomarkers for patient stratification and treatment response prediction.
dc.format.extent20 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec770672
dc.identifier.issn2234-943X
dc.identifier.pmid42137158
dc.identifier.urihttps://hdl.handle.net/2445/230319
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fonc.2026.1639330
dc.relation.ispartofFrontiers In Oncology, 2026, vol. 16
dc.relation.urihttps://doi.org/10.3389/fonc.2026.1639330
dc.rightscc-by (c) Quintás, G. et al., 2026
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationOncologia
dc.subject.classificationMarcadors bioquímics
dc.subject.otherOncology
dc.subject.otherBiochemical markers
dc.titleDistinct protein and metabolic profiles in patients with advanced clear-cell renal cell carcinoma treated with sunitinib: a study of the Spanish oncology genitourinary group
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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