NUK - logo
E-viri
Celotno besedilo
Recenzirano
  • 2 years versus 1 year of ad...
    Goldhirsch, Aron, Prof; Gelber, Richard D, Prof; Piccart-Gebhart, Martine J, Prof; de Azambuja, Evandro, MD; Procter, Marion, MSci; Suter, Thomas M, Prof; Jackisch, Christian, Prof; Cameron, David, Prof; Weber, Harald A, MD; Heinzmann, Dominik, PhD; Lago, Lissandra Dal, MD; McFadden, Eleanor, MA; Dowsett, Mitch, Prof; Untch, Michael, Prof; Gianni, Luca, MD; Bell, Richard, Prof; Köhne, Claus-Henning, Prof; Vindevoghel, Anita, MD; Andersson, Michael, MD; Brunt, A Murray, MD; Otero-Reyes, Douglas, MD; Song, Santai, MD; Smith, Ian, Prof; Leyland-Jones, Brian, PhD; Baselga, Jose, Prof

    The Lancet (British edition), 09/2013, Letnik: 382, Številka: 9897
    Journal Article

    Summary Background Trastuzumab has established efficacy against breast cancer with overexpression or amplification of the HER2 oncogene. The standard of care is 1 year of adjuvant trastuzumab, but the optimum duration of treatment is unknown. We compared 2 years of treatment with trastuzumab with 1 year of treatment, and updated the comparison of 1 year of trastuzumab versus observation at a median follow-up of 8 years, for patients enrolled in the HERceptin Adjuvant (HERA) trial. Methods The HERA trial is an international, multicentre, randomised, open-label, phase 3 trial comparing treatment with trastuzumab for 1 and 2 years with observation after standard neoadjuvant chemotherapy, adjuvant chemotherapy, or both in 5102 patients with HER2-positive early breast cancer. The primary endpoint was disease-free survival. The comparison of 2 years versus 1 year of trastuzumab treatment involved a landmark analysis of 3105 patients who were disease-free 12 months after randomisation to one of the trastuzumab groups, and was planned after observing at least 725 disease-free survival events. The updated intention-to-treat comparison of 1 year trastuzumab treatment versus observation alone in 3399 patients at a median follow-up of 8 years (range 0–10) is also reported. This study is registered with ClinicalTrials.gov , number NCT00045032. Findings We recorded 367 events of disease-free survival in 1552 patients in the 1 year group and 367 events in 1553 patients in the 2 year group (hazard ratio HR 0·99, 95% CI 0·85–1·14, p=0·86). Grade 3–4 adverse events and decreases in left ventricular ejection fraction during treatment were reported more frequently in the 2 year treatment group than in the 1 year group (342 20·4% vs 275 16·3% grade 3–4 adverse events, and 120 7·2% vs 69 4·1% decreases in left ventricular ejection fraction, respectively). HRs for a comparison of 1 year of trastuzumab treatment versus observation were 0·76 (95% CI 0·67–0·86, p<0·0001) for disease-free survival and 0·76 (0·65–0·88, p=0·0005) for overall survival, despite crossover of 884 (52%) patients from the observation group to trastuzumab therapy. Interpretation 2 years of adjuvant trastuzumab is not more effective than is 1 year of treatment for patients with HER2-positive early breast cancer. 1 year of treatment provides a significant disease-free and overall survival benefit compared with observation and remains the standard of care. Funding F Hoffmann-La Roche (Roche).