Trastuzumab for Patients With Axillary-Node–Positive Breast Cancer: Results of the FNCLCC-PACS 04 Trial

M. Spielmann(Institut Gustave Roussy), Henri Roché(Institut Gustave Roussy), T. Delozier(Institut Gustave Roussy), Jean-Luc Canon(Institut Gustave Roussy), Gilles Romieu(Institut Gustave Roussy), Hugues Bourgeois(Institut Gustave Roussy), Jean-Marc Extra(Institut Gustave Roussy), Daniel Serin(Institut Gustave Roussy), Pierre Kerbrat(Institut Gustave Roussy), Jean‐Pascal Machiels(Institut Gustave Roussy), Alain Lortholary(Institut Gustave Roussy), Hubert Orfeuvre(Institut Gustave Roussy), Mario Campone(Institut Gustave Roussy), Anne‐Claire Hardy‐Bessard(Institut Gustave Roussy), Bruno Coudert(Institut Gustave Roussy), Marie Maerevoet(Institut Gustave Roussy), G. Piot(Institut Gustave Roussy), Andrew Kramar(Institut Gustave Roussy), Anne-Laure Martin(Institut Gustave Roussy), Frédérique Penault–Llorca(Institut Gustave Roussy)
Journal of Clinical Oncology
November 17, 2009
Cited by 299

Abstract

PURPOSE: To evaluate the efficacy of trastuzumab in patients with node-positive breast cancer treated with surgery, adjuvant chemotherapy, radiotherapy, and hormone therapy if applicable. PATIENTS AND METHODS: Three thousand ten patients with operable node-positive breast cancer were randomly assigned to receive adjuvant anthracycline-based chemotherapy with or without docetaxel. Patients who presented human epidermal growth factor receptor 2 (HER2) -overexpressing tumors were secondary randomly assigned to either a sequential regimen of trastuzumab (6 mg/kg every 3 weeks) for 1 year or observation. The primary end point was disease-free survival (DFS). RESULTS: Overall 528 patients were randomly assigned between trastuzumab (n = 260) and observation (n = 268) arm. Of the 234 patients (90%) who received at least one administration of trastuzumab, 196 (84%) received at least 6 months of treatment, and 41 (18%) discontinued treatment due to cardiac events (any grade). At the date of analysis (October 2007), 129 DFS events were recorded. Random assignment to the trastuzumab arm was associated with a nonsignificant 14% reduction in the risk of relapse (hazard ratio, 0.86; 95% CI, 0.61 to 1.22; P = .41, log-rank stratified on pathologic node involvement). Three-year DFS rates were 78% (95% CI, 72.3 to 82.5) and 81% (95% CI, 75.3 to 85.4) in the observation and trastuzumab arms, respectively. CONCLUSION: After a 47-month median follow-up, 1 year of trastuzumab given sequentially after adjuvant chemotherapy was not associated with a statistically significant decrease in the risk of relapse.


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