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Bilateral breast cancer, synchronous and metachronous: Differences and outcome

  • J.J. Jobsen*
  • , J. van der Palen
  • , F. Ong
  • , S. Riemersma
  • , H. Struikmans
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

The aims of this study were twofold: to analyze the incidence of patients having synchronous or metachronous bilateral invasive breast cancer (SBBC and MBBC) and to assess the characteristics and outcome compared to those having unilateral breast cancer (UBC). The used data were obtained from our prospective population-based cohort study which had been started in 1983. Bilateral breast cancer (BBC) was categorized as SBBC (≤3 months of the first primary) or MBBC (>3 months after the first primary). The incidence of SBBC was 1 % and that of MBBC 7.0 %. Patients with UBC showed more ductal carcinoma compared to patients with BBC. MBBC status was an independent significant predictor of local failure (HR 1.9; 95 % CI 1.3–2.7). SBBC status was an independent predictor of distant metastases (HR 2.6; 95 % CI 1.4–4.5). Overall survival (OS) was better for MBBC (HR 0.6; 95 % CI 0.4–0.8) and worse for SBBC (HR 2.3; 95 % CI 1.5–3.6) compared to UBC. We noted: (1) MBBC showed a significant higher local failure compared to UBC, (2) SBBC, compared to MBBC and UBC had a significant higher distant metastases rate, (3) disease-specific survival and OS were significantly worse for SBBC compared to UBC and MBBC, and (4) that the OS for MBBC compared to UBC, was significantly better.
Original languageEnglish
Pages (from-to)277-283
Number of pages7
JournalBreast cancer research and treatment
Volume153
Issue number2
Early online date13 Aug 2015
DOIs
Publication statusPublished - Sept 2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Synchronous
  • Metachronous
  • Bilateral breast cancer
  • Incidence
  • Prognosis
  • n/a OA procedure

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