Gene signatures in patients with early breast cancer and relapse despite pathologic complete response

Altres autors/es

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

Data de publicació

2022-08-16T06:52:56Z

2022-08-16T06:52:56Z

2022-03-29



Resum

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.

Tipus de document

Article


Versió publicada

Llengua

Anglès

Publicat per

Springer Nature

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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