Comparative Analysis of Oncotype DX Recurrence Scores in Screen‑Detected Versus Symptomatic Early‑Stage Breast Cancer: The COSSEB Study

  • 0General and Breast Surgery, Mid and South Essex NHS Foundation Trust, Basildon, GBR.

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Summary

This summary is machine-generated.

Screen-detected breast cancers (SDBCs) and symptomatic breast cancers (SBCs) show similar genomic risk scores (Oncotype DX Recurrence Score). Presentation mode should not solely guide adjuvant chemotherapy decisions for early breast cancer.

Area Of Science

  • Oncology
  • Genomics
  • Breast Cancer Research

Background

  • Screen-detected breast cancers (SDBCs) and symptomatic breast cancers (SBCs) often present with differing stage and biology.
  • The 21-gene Oncotype DX Recurrence Score (ODX-RS) guides adjuvant treatment for ER-positive, HER2-negative early breast cancer.
  • Investigating genomic risk differences based on breast cancer presentation mode is crucial for treatment decisions.

Purpose Of The Study

  • To compare genomic risk, measured by ODX-RS, between SDBCs and SBCs.
  • To evaluate if the mode of breast cancer presentation influences adjuvant treatment recommendations.
  • To determine the impact of presentation mode on ODX-RS categories and subsequent treatment guidance.

Main Methods

  • Retrospective analysis of 200 women (≥50 years) with ER-positive, HER2-negative early breast cancer.
  • Cohort divided into 100 SDBCs and 100 age-matched SBCs with available ODX-RS testing.
  • Comparison of clinicopathologic features, ODX-RS categories (≤25 vs. ≥26), and treatment recommendations between groups.

Main Results

  • SDBCs were smaller and more frequently treated with breast-conserving surgery.
  • Low HER2 expression was more common in SDBCs.
  • ODX-RS distributions and adjuvant chemotherapy recommendations were largely similar between SDBCs and SBCs (19% vs. 23% recommended chemotherapy).

Conclusions

  • Screen-detected and symptomatic ER-positive/HER2-negative early breast cancers exhibit comparable ODX-RS distributions.
  • Presentation mode alone should not dictate adjuvant chemotherapy decisions; multigene testing is essential.
  • Individualized treatment planning requires ODX-RS and standard clinicopathologic factors; further prospective studies are warranted.