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Microbiome and response to therapy in triple negative breast cancer: a systematic review

datacite.subject.fosCiências Médicas
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorLopes, Mariana
dc.contributor.authorVila Nova, Carlos
dc.contributor.authorOliveira, Rui Caetano
dc.contributor.authorSchmitt, Fernando
dc.contributor.authorMendes, Fernando
dc.contributor.authorMartins, Diana
dc.date.accessioned2026-03-20T17:02:00Z
dc.date.available2026-03-20T17:02:00Z
dc.date.issued2026-03-20
dc.description.abstractObjectives: Triple-negative breast cancer (TNBC) accounts for approximately 15% of all invasive breast cancers and is characterized by aggressive behavior, limited therapeutic options, and poor clinical outcomes. Due to the absence of hormone receptors and HER2 expression, systemic treatment relies predominantly on chemotherapy, which is associated with high rates of early recurrence and mortality. Emerging evidence suggests that alterations in the microbiome can contribute to TNBC progression and influence therapeutic response, particularly affecting the efficacy of chemotherapy and immunotherapy through immune-mediated mechanisms; however, its role in TNBC remains incompletely understood. This systematic review aims to explore the role of the microbiome in TNBC. It specifically aims to understand if the microbiome influences complete pathological response in TNBC. Methods: This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A comprehensive literature search was performed in PubMed and Cochrane databases. Fourteen eligible studies were included, encompassing preclinical and clinical evidence. Results: The findings indicate that both gut and tumor-associated microbiota significantly influence therapeutic response in TNBC, especially in the context of neoadjuvant chemotherapy (NACT) and immune checkpoint blockade (ICB). Higher microbial diversity and the presence of specific commensal taxa were consistently associated with enhanced antitumor immune activation, increased immune cell infiltration, and improved treatment efficacy. Conversely, antibiotic-induced dysbiosis was linked to reduced pCR rates and poorer clinical outcomes. Microbiome-modulating interventions demonstrated potential in restoring eubiosis and enhancing therapeutic responsiveness. Conclusions: Overall, the available evidence supports the microbiome as a promising biomarker and therapeutic target for optimizing treatment strategies and improving outcomes in TNBCpor
dc.identifier.doi10.32604/or.2026.074215
dc.identifier.eissn1555-3906
dc.identifier.urihttp://hdl.handle.net/10400.26/62338
dc.language.isoeng
dc.peerreviewedyes
dc.publisherTech Science Press
dc.relationThis project was supported by FCT/MCTES UIDP/05608/2020 (https://doi.org/10.54499/UIDP/ 05608/2020) and UIDB/05608/2020 (https://doi.org/10.54499/UIDB/05608/2020) Institutional.
dc.relation.hasversionhttp://doi.org/10.32604/or.2026.074215
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectmicrobiota
dc.subjectchemotherapy
dc.subjectpathological complete response
dc.subjectimmunotherapy
dc.subjecttriple negative breast neoplasms
dc.titleMicrobiome and response to therapy in triple negative breast cancer: a systematic reviewpor
dc.typetext
dcterms.referencesThe supplementary material is available online at https://www.techscience.com/doi/10.3 2604/or.2026.074215/s1.
dspace.entity.typePublication
oaire.citation.endPage47
oaire.citation.startPage1
oaire.citation.titleOncology Research
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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