Multiplexed high-throughput immune cell imaging in patients with high-risk triple negative early breast cancer: Analysis from the International Breast Cancer Study Group (IBCSG) Trial 22-00.

Détails

ID Serval
serval:BIB_4DE560AF185F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Multiplexed high-throughput immune cell imaging in patients with high-risk triple negative early breast cancer: Analysis from the International Breast Cancer Study Group (IBCSG) Trial 22-00.
Périodique
European journal of cancer
Auteur⸱e⸱s
Rusakiewicz S., Tyekucheva S., Tissot-Renaud S., Chaba K., Imbimbo M., Benedetti F., Kammler R., Hornfeld J., Munzone E., Gianni L., Thurlimann B., Láng I., Pruneri G., Gray K.P., Regan M.R., Loi S., Colleoni M., Viale G., Kandalaft L., Coukos G., Curigliano G.
ISSN
1879-0852 (Electronic)
ISSN-L
0959-8049
Statut éditorial
Publié
Date de publication
03/2024
Peer-reviewed
Oui
Volume
200
Pages
113535
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Triple-negative breast cancer (TNBC) is the most aggressive breast cancer (BC) subtype, with dismal prognosis and limited option in advanced settings, yet stromal tumor infiltrating lymphocytes (sTILs) in this subtype has a predictive role.
The International Breast Cancer Study Group (IBCSG) Trial 22-00 is a randomized phase III clinical trial testing the efficacy of low-dose metronomic oral Cyclophosphamide-Methotrexate (CM) maintenance following standard adjuvant chemotherapy treatment for early-stage hormone receptor-negative breast cancer patients. A case-cohort sampling was used. We characterized immune cells infiltrates in patients with TNBC by 6 plex immunofluorescence (IF) staining for CD4, FOXP3, CD3, cytokeratine and CD8 RESULTS: We confirmed that high immune CD3 <sup>+</sup> T cells as well as stromal and intra-epithelial Tregs (CD4 <sup>+</sup> Foxp3 <sup>+</sup> T cells) infiltrates were associated with a better Distant Recurrence-Free Interval (DRFI), especially in LN+ patient, regardless of the treatment. More importantly, we showed that the spatial distribution of immune cells at baseline is crucial, as CM maintenance was detrimental for T cells excluded LN+ TNBC patients.
immune spatial classification on immune cells infiltrates seems crucial and could help patients' selection in clinical trial and greatly improve responses to specific therapies.
Mots-clé
Humans, Biomarkers, Tumor/analysis, Cyclophosphamide, Disease-Free Survival, Forkhead Transcription Factors, Lymphocytes, Tumor-Infiltrating, Methotrexate, Prognosis, Triple Negative Breast Neoplasms/diagnostic imaging, Triple Negative Breast Neoplasms/drug therapy, Female, Randomized Controlled Trials as Topic, Clinical Trials, Phase III as Topic, Multiplexed analysis, Multispectral Imaging, Triple negative breast cancer, Tumor infiltrating lymphocytes
Pubmed
Web of science
Création de la notice
09/02/2024 14:06
Dernière modification de la notice
26/03/2024 8:10
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