Abstract

SummaryBackgroundAdjuvant trastuzumab significantly improves outcomes for patients with HER2-positive early breast cancer. The standard treatment duration is 12 months but shorter treatment could provide similar efficacy while reducing toxicities and cost. We aimed to investigate whether 6-month adjuvant trastuzumab treatment is non-inferior to the standard 12-month treatment regarding disease-free survival.MethodsThis study is an open-label, randomised phase 3 non-inferiority trial. Patients were recruited from 152 centres in the UK. We randomly assigned patients with HER2-positive early breast cancer, aged 18 years or older, and with a clear indication for chemotherapy, by a computerised minimisation process (1:1), to receive either 6-month or 12-month trastuzumab delivered every 3 weeks intravenously (loading dose of 8 mg/kg followed by maintenance doses of 6 mg/kg) or subcutaneously (600 mg), given in combination with chemotherapy (concurrently or sequentially). The primary endpoint was disease-free survival, analysed by intention to treat, with a non-inferiority margin of 3% for 4-year disease-free survival. Safety was analysed in all patients who received trastuzumab. This trial is registered with EudraCT (number 2006–007018–39), ISRCTN (number 52968807), and ClinicalTrials.gov (number NCT00712140).FindingsBetween Oct 4, 2007, and July 31, 2015, 2045 patients were assigned to 12-month trastuzumab treatment and 2044 to 6-month treatment (one patient was excluded because they were double randomised). Median follow-up was 5·4 years (IQR 3·6–6·7) for both treatment groups, during which a disease-free survival event occurred in 265 (13%) of 2043 patients in the 6-month group and 247 (12%) of 2045 patients in the 12-month group. 4-year disease-free survival was 89·4% (95% CI 87·9–90·7) in the 6-month group and 89·8% (88·3–91·1) in the 12-month group (hazard ratio 1·07 [90% CI 0·93–1·24], non-inferiority p=0·011), showing non-inferiority of the 6-month treatment. 6-month trastuzumab treatment resulted in fewer patients reporting severe adverse events (373 [19%] of 1939 patients vs 459 [24%] of 1894 patients, p=0·0002) or stopping early because of cardiotoxicity (61 [3%] of 1939 patients vs 146 [8%] of 1894 patients, p<0·0001).InterpretationWe have shown that 6-month trastuzumab treatment is non-inferior to 12-month treatment in patients with HER2-positive early breast cancer, with less cardiotoxicity and fewer severe adverse events. These results support consideration of reduced duration trastuzumab for women at similar risk of recurrence as to those included in the trial.FundingUK National Institute for Health Research, Health Technology Assessment Programme.

Highlights

  • Interpretation We have shown that 6-month trastuzumab treatment is non-inferior to 12-month treatment in patients with HER2-positive early breast cancer, with less cardiotoxicity and fewer severe adverse events

  • Results from the FinHer trial,[7] which randomly assigned patients to adjuvant chemotherapy with or without 9 weeks of concurrent trastuzumab, showed a statistically sig­nificant improvement in disease-free survival for patients assigned to trastuzumab and generated considerable interest in the possibility of shorter trastu­ zumab durations than the standard treatment time

  • We found three randomised controlled trials of adjuvant trastuzumab added to chemotherapy versus chemotherapy alone for patients with HER2-positive early breast cancer

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Summary

Introduction

Trastuzumab delivered with chemotherapy for patients with HER2-positive breast cancer in the metastatic[1] and adjuvant settings[2,3,4] resulted in improved treatment outcomes, and long-term follow-up has confirmed these benefits.[5,6] A 12-month treatment duration with adjuvant trastuzumab was chosen arbitrarily for the pivotal licensing trials[2,3,4] and, subseq­uently, became standard. Norwich, UK (A N Harnett); Medical Oncology, Mount Vernon Cancer Centre, Northwood, UK (M-L Ah-See MD, Prof D Miles MD); Sussex Cancer. Brighton and Sussex University Hospitals NHS, Brighton, UK (R Simcock FRCR); Cancer Research UK Clinical Trials Unit and Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK (Prof D Rea FRCP); Department of Oncology, Southampton University Hospital NHS Foundation Trust, Southampton, UK (S Raj MBBS); Department of Oncology, Royal.

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