Linking tumor immune infiltration to enhanced longevity in recurrence-free breast cancer

dc.contributor.authorAngelats, Laura
dc.contributor.authorParé Brunet, Laia
dc.contributor.authorRubio-Perez, Carlota
dc.contributor.authorSanfeliu, Esther
dc.contributor.authorGonzález,A.
dc.contributor.authorSeguí, Elia
dc.contributor.authorVillacampa, Guillermo
dc.contributor.authorMarín Aguilera, Mercedes
dc.contributor.authorPernas, Sònia
dc.contributor.authorConte, Benedetta
dc.contributor.authorAlbarrán Fernández, Víctor
dc.contributor.authorMartínez Sáez, Olga
dc.contributor.authorAguirre, Ángela
dc.contributor.authorGalván, Patricia
dc.contributor.authorFernández Martínez, Aranzazu
dc.contributor.authorCobo, Sara
dc.contributor.authorRey, Montse
dc.contributor.authorMartínez Romero, Anabel
dc.contributor.authorWalbaum, Benjamin
dc.contributor.authorSchettini, Francesco
dc.contributor.authorVidal Losada, Maria Jesús
dc.contributor.authorBuckingham, Wesley
dc.contributor.authorMuñoz, M.
dc.contributor.authorAdamo, Barbara
dc.contributor.authorAgrawal, Yash
dc.contributor.authorGuedán Carrió, Sònia
dc.contributor.authorPascual, Tomás
dc.contributor.authorAgudo, Judith
dc.contributor.authorGrzelak, M.
dc.contributor.authorBorcherding, Nicholas
dc.contributor.authorHeyn, Holguer
dc.contributor.authorVivancos, Ana
dc.contributor.authorParker, Joel S.
dc.contributor.authorVillagrasa, Patricia
dc.contributor.authorPerou, Charles M.
dc.contributor.authorPrat Aparicio, Aleix
dc.contributor.authorBrasó Maristany, Fara
dc.date.accessioned2025-04-08T17:56:43Z
dc.date.available2025-04-08T17:56:43Z
dc.date.issued2025-01-01
dc.date.updated2025-04-08T17:56:43Z
dc.description.abstractBackground: The infiltration of tumor-infiltrating B cells and plasma cells in early-stage breast cancer has been associated with a reduced risk of distant metastasis. However, the influence of B-cell tumor infiltration on overall patient survival remains unclear. Materials and methods: This study explored the relationship between an antitumor immune response, measured by a 14-gene B-cell/immunoglobulin (IGG) signature, and mortality risk in 9638 breast cancer patients across three datasets. Associations with tumor subtype, stage, and age were examined. IGG was characterized using spatial GeoMx profiling and single-cell RNA sequencing, and its relationship with tertiary lymphoid structures (TLSs) was evaluated. The predictive value of each of the 14 IGG genes for B-cell receptor (BCR) and T-cell receptor (TCR) clonality and longevity was also assessed, along with its association with longevity in other cancer types. Results: High IGG signature expression was significantly associated with a 41%-47% reduction in death risk in breast cancer survivors (P < 0.001), regardless of age, tumor stage, or subtype. Similar associations were observed in other cancers, including melanoma. In breast cancer, the IGG signature was significantly linked to overall survival without relapse in patients aged 41-70 years at diagnosis. Additionally, IGG expression correlated with the presence of TLSs and higher B- and T-cell polyclonality. A specific subset of seven IGG genes strongly correlated with BCR and TCR clonality, with predictive power for identifying clonality and improved longevity, especially when combining two of these genes. Conclusions: This study uncovers a significant link between immune gene expression in tumors and extended longevity in breast cancer survivors, even in the absence of recurrence. The IGG signature, particularly its key gene subset, emerges as a powerful marker of sustained antitumor immunity and overall patient fitness. These findings pave the way for personalized treatment strategies that enhance both survival and long-term health outcomes.
dc.format.extent11 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec758007
dc.identifier.issn2059-7029
dc.identifier.pmid39765189
dc.identifier.urihttps://hdl.handle.net/2445/220349
dc.language.isoeng
dc.publisherElsevier
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.esmoop.2024.104109
dc.relation.ispartofESMO Open, 2025, vol. 10, num.1
dc.relation.urihttps://doi.org/10.1016/j.esmoop.2024.104109
dc.rightscc-by-nc-nd (c) Angelats, Laura et al., 2025
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationResposta immunitària
dc.subject.classificationLongevitat
dc.subject.classificationLimfòcits
dc.subject.classificationCàncer de mama
dc.subject.classificationCèl·lules T
dc.subject.classificationExpressió gènica
dc.subject.otherImmune response
dc.subject.otherLongevity
dc.subject.otherLymphocytes
dc.subject.otherBreast cancer
dc.subject.otherT cells
dc.subject.otherGene expression
dc.titleLinking tumor immune infiltration to enhanced longevity in recurrence-free breast cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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