Trastuzumab after Adjuvant Chemotherapy in HER2-Positive Breast Cancer

Martine Piccart(Institut Jules Bordet), Marion Procter(European Institute of Oncology), Brian Leyland‐Jones(McGill University), Aron Goldhirsch(Institute of Oncology Research), Michael Untch(Klinik für Frauenheilkunde), Ian Smith(Royal Marsden Hospital), Luca Gianni(Fondazione IRCCS Istituto Nazionale dei Tumori), José Baselga(Hebron University), Richard H. Bell(Geelong Hospital), Christian Jackisch(Philipps University of Marburg), David Cameron(Western General Hospital), Mitch Dowsett(National Health Service), Carlos H. Barrios(Pontifícia Universidade Católica do Rio Grande do Sul), Günther Steger(Medical University of Vienna), Chiun‐Sheng Huang(National Taiwan University Hospital), Michael Andersson(Rigshospitalet), Moshe Inbar(Tel Aviv Sourasky Medical Center), Mikhail Lichinitser(Russian Cancer Research Center NN Blokhin), István Láng(National Institute of Oncology), Ulrike Nitz(Heinrich Heine University Düsseldorf), Hiroji Iwata(Aichi Cancer Center), Christoph Thomssen(University Medical Center Hamburg-Eppendorf), Caroline Lohrisch(BC Cancer Agency), Thomas Suter, Josef Rüschoff(Klinikum Kassel), Tamás Sütö(Roche (Switzerland)), Victoria Greatorex(Roche (Switzerland)), Carol Ward(Roche (Switzerland)), Carolyn Straehle(Breast International Group), Eleanor McFadden(European Institute of Oncology), Mirko Dolci(Université Libre de Bruxelles), Richard D. Gelber(Dana-Farber Cancer Institute)
New England Journal of Medicine
October 20, 2005
Cited by 5,093Open Access
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Abstract

BACKGROUND: Trastuzumab, a recombinant monoclonal antibody against HER2, has clinical activity in advanced breast cancer that overexpresses HER2. We investigated its efficacy and safety after excision of early-stage breast cancer and completion of chemotherapy. METHODS: This international, multicenter, randomized trial compared one or two years of trastuzumab given every three weeks with observation in patients with HER2-positive and either node-negative or node-positive breast cancer who had completed locoregional therapy and at least four cycles of neoadjuvant or adjuvant chemotherapy. RESULTS: Data were available for 1694 women randomly assigned to two years of treatment with trastuzumab, 1694 women assigned to one year of trastuzumab, and 1693 women assigned to observation. We report here the results only of treatment with trastuzumab for one year or observation. At the first planned interim analysis (median follow-up of one year), 347 events (recurrence of breast cancer, contralateral breast cancer, second nonbreast malignant disease, or death) were observed: 127 events in the trastuzumab group and 220 in the observation group. The unadjusted hazard ratio for an event in the trastuzumab group, as compared with the observation group, was 0.54 (95 percent confidence interval, 0.43 to 0.67; P<0.0001 by the log-rank test, crossing the interim analysis boundary), representing an absolute benefit in terms of disease-free survival at two years of 8.4 percentage points. Overall survival in the two groups was not significantly different (29 deaths with trastuzumab vs. 37 with observation). Severe cardiotoxicity developed in 0.5 percent of the women who were treated with trastuzumab. CONCLUSIONS: One year of treatment with trastuzumab after adjuvant chemotherapy significantly improves disease-free survival among women with HER2-positive breast cancer. (ClinicalTrials.gov number, NCT00045032.)


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