Meta-Analysis of Breast Cancer Outcomes in Adjuvant Trials of Aromatase Inhibitors Versus Tamoxifen

Author:

Dowsett Mitch1,Cuzick Jack1,Ingle Jim1,Coates Alan1,Forbes John1,Bliss Judith1,Buyse Marc1,Baum Michael1,Buzdar Aman1,Colleoni Marco1,Coombes Charles1,Snowdon Claire1,Gnant Michael1,Jakesz Raimund1,Kaufmann Manfred1,Boccardo Francesco1,Godwin Jon1,Davies Christina1,Peto Richard1

Affiliation:

1. From the Academic Department of Biochemistry, Royal Marsden Hospital; Cancer Research UK Centre for Epidemiology, Mathematics and Statistics, Queen Mary University of London; Clinical Trials Group, Royal Free and University College London Medical School; Department of Cancer Medicine, Charing Cross Hospital, London; Clinical Trials and Statistics Unit, The Institute of Cancer Research, Surrey; Clinical Trials Service Unit and Epidemiological Studies Unit, University of Oxford, Oxford, United Kingdom;...

Abstract

Purpose To conduct meta-analyses of randomized trials of aromatase inhibitors (AIs) compared with tamoxifen either as initial monotherapy (cohort 1) or after 2 to 3 years of tamoxifen (cohort 2). Materials and Methods Data submitted to the Early Breast Cancer Trialists' Collaborative Group were used in separate meta-analyses of two cohorts. Primary analyses involve postmenopausal women with tumors reported to be estrogen receptor positive. Log-rank P values are two-sided. Results Cohort 1 comprised 9,856 patients with a mean of 5.8 years of follow-up. At 5 years, AI therapy was associated with an absolute 2.9% (SE = 0.7%) decrease in recurrence (9.6% for AI v 12.6% for tamoxifen; 2P < .00001) and a nonsignificant absolute 1.1% (SE = 0.5%) decrease in breast cancer mortality (4.8% for AI v 5.9% for tamoxifen; 2P = .1). Cohort 2 comprised 9,015 patients with a mean of 3.9 years of follow-up. At 3 years from treatment divergence (ie, approximately 5 years after starting hormonal treatment), AI therapy was associated with an absolute 3.1% (SE = 0.6%) decrease in recurrence (5.0% for AI v 8.1% for tamoxifen since divergence; 2P < .00001) and an absolute 0.7% (SE = 0.3%) decrease in breast cancer mortality (1.7% for AI v 2.4% for tamoxifen since divergence; 2P = .02). There was no convincing heterogeneity in the proportional recurrence reduction with respect to age, nodal status, tumor grade, or progesterone receptor status and no indication of an increase in nonbreast deaths with AIs in either cohort. Conclusion AIs produce significantly lower recurrence rates compared with tamoxifen, either as initial monotherapy or after 2 to 3 years of tamoxifen. Additional follow-up will provide clearer information on long-term survival.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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