Estrogen Receptor Expression and Docetaxel Efficacy in Patients with Metastatic Breast Cancer: A Pooled Analysis of Four Randomized Trials

Author:

Andre Fabrice12,Broglio Kristine3,Pusztai Lajos1,Berrada Narjiss2,Mackey John R.4,Nabholtz Jean Marc5,Chan Stephen6,Hortobagyi Gabriel N.1

Affiliation:

1. a Department of Breast Medical Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas, USA

2. c Breast Cancer Unit, Department of Medical Oncology and UPRES EA03535 Institut Gustave Roussy, Villejuif, France

3. b Division of Quantitative Sciences, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas, USA

4. d Department of Oncology, University of Alberta, Edmonton, Alberta, Canada

5. e Department of Medical Oncology, Centre Jean Perrin, Clermont-Ferrand, France

6. f Nottingham City Hospital, Nottingham, United Kingdom

Abstract

Abstract Background. Differences in the efficacy of various chemotherapies in patients with estrogen receptor (ER)+ metastatic breast cancer are not well understood. In the present study, we assessed the efficacy of docetaxel in patients with metastatic breast cancer according to ER expression. Methods. The efficacy of docetaxel in terms of the response rate and progression-free survival (PFS) time was analyzed according to ER expression in four randomized trials comparing a docetaxel-based regimen with a nontaxane regimen that included a total of 1,631 patients. The odds ratio for tumor response was estimated with logistic regression and a hazard ratio (HR) for PFS was estimated with Cox proportional hazards models. Findings. ER expression was assessable in 1,037 patients included in these trials (64%). ER was expressed in 601 tumors (58%). Docetaxel was associated with a similarly higher response rate in both patients with ER+ (odds ratio, 2.90; 95% confidence interval [CI], 1.72–4.87) and patients with ER− (odds ratio, 2.55; 95% CI, 1.44–4.51) disease. The lower hazard for disease progression with docetaxel was also similar in ER+ (HR, 0.82; 95% CI, 0.67–1.00) and ER− (HR, 0.86; 95% CI, 0.70–1.07) cancers. The effect of docetaxel was not different in ER+ and ER− disease, in terms of both the response rate and PFS time (interaction test, p = .77 and p = .93). Interpretation. Docetaxel produces a higher response rate and lower risk for disease progression to a statistically similar extent in both patients with ER+ and patients with ER− metastatic breast cancer.

Funder

American Society of Clinical Oncology

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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