Ki-67 as prognostic marker in early breast cancer: a meta-analysis of published studies involving 12 155 patients

Evandro de Azambuja(Institut Jules Bordet), Fátima Cardoso(Institut Jules Bordet), Gilberto de Castro(Institut Jules Bordet), Maria Antonietta Colozza(Azienda Ospedaliera di Perugia), Max S. Mano(Institut Jules Bordet), Virginie Durbecq(Institut Jules Bordet), Christos Sotiriou(Institut Jules Bordet), Denis Larsimont(Institut Jules Bordet), M. Piccart-Gebhart(Institut Jules Bordet), Marianne Paesmans(Institut Jules Bordet)
British Journal of Cancer
April 24, 2007
Cited by 958Open Access
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Abstract

The Ki-67 antigen is used to evaluate the proliferative activity of breast cancer (BC); however, Ki-67's role as a prognostic marker in BC is still undefined. In order to better define the prognostic value of Ki-67/MIB-1, we performed a meta-analysis of studies that evaluated the impact of Ki-67/MIB-1 on disease-free survival (DFS) and/or on overall survival (OS) in early BC. Sixty-eight studies were identified and 46 studies including 12 155 patients were evaluable for our meta-analysis; 38 studies were evaluable for the aggregation of results for DFS, and 35 studies for OS. Patients were considered to present positive tumours for the expression of Ki-67/MIB-1 according to the cut-off points defined by the authors. Ki-67/MIB-1 positivity is associated with higher probability of relapse in all patients (HR=1.93 (95% confidence interval (CI): 1.74-2.14); P<0.001), in node-negative patients (HR=2.31 (95% CI: 1.83-2.92); P<0.001) and in node-positive patients (HR=1.59 (95% CI: 1.35-1.87); P<0.001). Furthermore, Ki-67/MIB-1 positivity is associated with worse survival in all patients (HR=1.95 (95% CI: 1.70-2.24; P<0.001)), node-negative patients (HR=2.54 (95% CI: 1.65-3.91); P<0.001) and node-positive patients (HR=2.33 (95% CI: 1.83-2.95); P<0.001). Our meta-analysis suggests that Ki-67/MIB-1 positivity confers a higher risk of relapse and a worse survival in patients with early BC.


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