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Tamoxifen-predictive value of gene expression signatures in premenopausal breast cancer: data from the randomized SBII:2 trial

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  • معلومة اضافية
    • بيانات النشر:
      Linköpings universitet, Avdelningen för kirurgi, ortopedi och onkologi
      Linköpings universitet, Medicinska fakulteten
      Region Östergötland, Onkologiska kliniken US
      Reg Jonkoping Cty, Sweden; Lund Univ, Sweden
      Lund Univ, Sweden
      NanoString Technol Inc, WA USA
      Reg Jonkoping Cty, Sweden
      Lund Univ, Sweden; Skane Univ Hosp, Sweden
      BMC
    • الموضوع:
      2023
    • Collection:
      Linköping University Electronic Press (LiU E-Press)
    • نبذة مختصرة :
      Background: Gene expression (GEX) signatures in breast cancer provide prognostic information, but little is known about their predictive value for tamoxifen treatment. We examined the tamoxifen-predictive value and prognostic effects of different GEX signatures in premenopausal women with early breast cancer. Methods: RNA from formalin-fixed paraffin-embedded tumor tissue from premenopausal women randomized between two years of tamoxifen treatment and no systemic treatment was extracted and successfully subjected to GEX profiling (n = 437, NanoString Breast Cancer 360 (TM) panel). The median follow-up periods for a recurrence-free interval (RFi) and overall survival (OS) were 28 and 33 years, respectively. Associations between GEX signatures and tamoxifen effect were assessed in patients with estrogen receptor-positive/human epidermal growth factor receptor 2-negative (ER+ /HER2-) tumors using Kaplan-Meier estimates and Cox regression. The prognostic effects of GEX signatures were studied in the entire cohort. False discovery rate adjustments (q-values) were applied to account for multiple hypothesis testing. Results: In patients with ER+/HER2- tumors, FOXA1 expression below the median was associated with an improved effect of tamoxifen after 10 years with regard to RFi (hazard ratio [HR](FOXA1(high)) = 1.04, 95% CI = 0.61-1.76, HRFOXA1(low) = 0.30, 95% CI = 0.14-0.67, q(interaction) = 0.0013), and a resembling trend was observed for AR (HRAR(high) = 1.15, 95% CI = 0.60-2.20, HRAR(low) = 0.42, 95% CI = 0.24-0.75, q(interaction) = 0.87). Similar patterns were observed for OS. Tamoxifen was in the same subgroup most beneficial for RFi in patients with low ESR1 expression (HRRFi ESR1(high) = 0.76, 95% CI = 0.43-1.35, HRRFi, ESR1(low) = 0.56, 95% CI = 0.29-1.06, q(interaction) = 0.37). Irrespective of molecular subtype, higher levels of ESR1, Mast cells, and PGR on a continuous scale were correlated with improved 10 years RFi (HRESR1 = 0.80, 95% CI = 0.69-0.92, q = 0.005; HRMast cells = 0.74, 95% CI = 0.65-0.85, q ...
    • File Description:
      application/pdf
    • Relation:
      Breast Cancer Research, 1465-5411, 2023, 25:1; orcid:0000-0002-8290-0592; http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-198665; PMID 37773134; ISI:001078566200001
    • الرقم المعرف:
      10.1186/s13058-023-01719-z
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.6402A1B8