Institut Català de la Salut
[Bruzas S] Interdisciplinary Breast Unit, Kliniken Essen-Mitte, Essen, Germany. [Gluz O] West German Study Group, Moenchengladbach, Germany. Breast Center Niederrhein, Evangelical Hospital Bethesda, Moenchengladbach, Germany. [Harbeck N] Breast Center, Dept. OB&GYN and CCCLMU, University of Munich (LMU), Munich, Germany. [Schmid P] Barts Cancer Institute, Queen Mary University London, London, United Kingdom. [Cortés J] International Breast Cancer Centre (IBCC), Quiron Group, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Medica Scientia Innovation Research (MEDSIR), Barcelona, Spain. Medica Scientia Innovation Research (MEDSIR), Ridgewood, NJ, USA. [Blohmer J] Klinik für Gynäkologie mit Brustzentrum, Charité-Universitätsmedizin Berlin, Berlin, Germany
Vall d'Hebron Barcelona Hospital Campus
2022-08-16T06:52:56Z
2022-08-16T06:52:56Z
2022-03-29
Prognostic markers; Tumour biomarkers
Marcadores pronósticos; Biomarcadores tumorales
Marcadors pronòstics; Biomarcadors tumorals
A substantial minority of early breast cancer (EBC) patients relapse despite their tumors achieving pathologic complete response (pCR) after neoadjuvant therapy. We compared gene expression (BC360; nCounter® platform; NanoString) between primary tumors of patients with post-pCR relapse (N = 14) with: (i) matched recurrent tumors from same patient (intraindividual analysis); and (ii) primary tumors from matched controls with pCR and no relapse (N = 41; interindividual analysis). Intraindividual analysis showed lower estrogen receptor signaling signature expression in recurrent tumors versus primaries (logFC = −0.595; P = 0.022). Recurrent tumors in patients with distant metastases also exhibited reduced expression of immune-related expression parameters. In interindividual analyses, primary tumor major histocompatibility complex class II expression was lower versus controls in patients with any relapse (logFC = −0.819; P = 0.030) or distant relapse (logFC = −1.151; P = 0.013). Primaries with later distant relapse also had greater homologous recombination deficiency than controls (logFC = 0.649; P = 0.026). Although no associations remained statistically significant following adjustment for false discovery rate, our results show that transcriptomic analyses have potential for prognostic value and may help in selecting optimal treatment regimens for EBC at risk of relapse and warrant further investigation.
Article
Published version
English
Mama - Càncer - Aspectes genètics; Mama - Càncer - Recaiguda; DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms; Other subheadings::Other subheadings::Other subheadings::/genetics; DISEASES::Neoplasms::Neoplastic Processes::Neoplasm Recurrence, Local; ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama; Otros calificadores::Otros calificadores::Otros calificadores::/genética; ENFERMEDADES::neoplasias::procesos neoplásicos::recurrencia neoplásica local
Springer Nature
NPJ Breast Cancer;8
https://doi.org/10.1038/s41523-022-00403-3
Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/