Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/220349
Title: Linking tumor immune infiltration to enhanced longevity in recurrence-free breast cancer
Author: Angelats, Laura
Paré Brunet, Laia
Rubio-Perez, Carlota
Sanfeliu, Esther
González,A.
Seguí, Elia
Villacampa, Guillermo
Marín Aguilera, Mercedes
Pernas, Sònia
Conte, Benedetta
Albarrán Fernández, Víctor
Martínez Sáez, Olga
Aguirre, Ángela
Galván, Patricia
Fernández Martínez, Aranzazu
Cobo, Sara
Rey, Montse
Martínez Romero, Anabel
Walbaum, Benjamin
Schettini, Francesco
Vidal Losada, Maria Jesús
Buckingham, Wesley
Muñoz, M.
Adamo, Barbara
Agrawal, Yash
Guedán Carrió, Sònia
Pascual, Tomás
Agudo, Judith
Grzelak, M.
Borcherding, Nicholas
Heyn, Holguer
Vivancos, Ana
Parker, Joel S.
Villagrasa, Patricia
Perou, Charles M.
Prat Aparicio, Aleix
Brasó Maristany, Fara
Keywords: Resposta immunitària
Longevitat
Limfòcits
Càncer de mama
Cèl·lules T
Expressió gènica
Immune response
Longevity
Lymphocytes
Breast cancer
T cells
Gene expression
Issue Date: 1-Jan-2025
Publisher: Elsevier
Abstract: Background: 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.
Note: Reproducció del document publicat a: https://doi.org/10.1016/j.esmoop.2024.104109
It is part of: ESMO Open, 2025, vol. 10, num.1
URI: https://hdl.handle.net/2445/220349
Related resource: https://doi.org/10.1016/j.esmoop.2024.104109
ISSN: 2059-7029
Appears in Collections:Articles publicats en revistes (Medicina)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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