Prognosis in women with small (T1mic,T1a,T1b) node-negative operable breast cancer by immunohistochemically selected subtypes

Prognosis in women with small (T1mic,T1a,T1b) node-negative operable breast cancer by immunohistochemically selected subtypes

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : G. Cancello P. Maisonneuve N. Rotmensz G. Viale M. G. Mastropasqua G. Pruneri E. Montagna S. Dellapasqua M. Iorfida A. Cardillo
  • چاپ و سال / کشور: 2011

Description

Knowledge is limited about prognostic significance of breast cancer subtypes among women with small invasive node-negative breast tumours. We explored patterns of recurrence in 1691 women with pT1mic/T1a/T1b, pN0 and M0 breast cancer according to four immunohistochemically defined tumour subtypes: (i) Luminal A (ERpositive, PgR-positive, HER2-negative and Ki-67\14%); (ii) Luminal B (ER-positive and/or PgR-positive, HER2- positive and/or Ki-67 C 14%); (iii) HER2-positive, both endocrine receptors absent; and (iv) Triple Negative. At multivariate analysis, women with the Triple Negative breast cancer subtype had an increased risk of loco-regional relapse (LRR) (Hazards Ratio (HR) 3.58; 95%CI: 1.40–9.13) and breast cancer related events (HR 2.18; 95%CI: 1.04–4.57). Overall, Luminal B subtype was not associated with a statistically significant increased risk of recurrence compared with Luminal A, while patients with Luminal B subtype tumours overexpressing HER2 had a 2 fold risk of reduced breast cancer related survival (BCS), but not an increased risk of LRR and distant metastases. Women with HER2 breast cancer subtype had a statistically significant increased risk of LRR (HR 4.53; 95%CI: 1.56–13.1), distant metastases and reduced BCS (HR 3.22; 95%CI: 1.44–7.18) and overall survival (HR 2.87; 95%CI: 1.05–7.89) when compared with the Luminal A subtype, at multivariate analysis. In conclusion, women with small size, node-negative, breast cancer are at higher risk of relapse if with HER2-positive endocrine receptor absent or Triple Negative disease.
Breast Cancer Res Treat (2011) 127:713–720 DOI 10.1007/s10549-011-1465-7 Received: 16 February 2011 / Accepted: 16 March 2011 / Published online: 31 March 2011  Springer Science+Business Media, LLC. 2011
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