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Article: 2 years versus 1 year of adjuvant trastuzumab for HER2-positive breast cancer (HERA): an open-label, randomised controlled trial
Title | 2 years versus 1 year of adjuvant trastuzumab for HER2-positive breast cancer (HERA): an open-label, randomised controlled trial |
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Authors | |
Issue Date | 2013 |
Publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/locate/lancet |
Citation | The Lancet, 2013, v. 382 n. 9897, p. 1021-1028 How to Cite? |
Abstract | 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. |
Persistent Identifier | http://hdl.handle.net/10722/251820 |
ISSN | 2023 Impact Factor: 98.4 2023 SCImago Journal Rankings: 12.113 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Goldhirsch, A | - |
dc.contributor.author | Gelber, RD | - |
dc.contributor.author | Piccart-Gebhart, MJ | - |
dc.contributor.author | de Azambuja, E | - |
dc.contributor.author | Procter, M | - |
dc.contributor.author | Suter, TM | - |
dc.contributor.author | Jackisch, C | - |
dc.contributor.author | Cameron, D | - |
dc.contributor.author | Weber, HA | - |
dc.contributor.author | Heinzmann, D | - |
dc.contributor.author | Lago, LD | - |
dc.contributor.author | McFadden, E | - |
dc.contributor.author | Dowsett, M | - |
dc.contributor.author | Untch, M | - |
dc.contributor.author | Gianni, L | - |
dc.contributor.author | Bell, R | - |
dc.contributor.author | Köhne, CH | - |
dc.contributor.author | Vindevoghel, A | - |
dc.contributor.author | Andersson, M | - |
dc.contributor.author | Brunt, AM | - |
dc.contributor.author | Otero-Reyes, D | - |
dc.contributor.author | Song, S | - |
dc.contributor.author | Smith, I | - |
dc.contributor.author | Leyland-Jones, B | - |
dc.contributor.author | Baselga, J | - |
dc.contributor.author | Kwong, A | - |
dc.date.accessioned | 2018-03-19T07:01:47Z | - |
dc.date.available | 2018-03-19T07:01:47Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | The Lancet, 2013, v. 382 n. 9897, p. 1021-1028 | - |
dc.identifier.issn | 0140-6736 | - |
dc.identifier.uri | http://hdl.handle.net/10722/251820 | - |
dc.description.abstract | 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. | - |
dc.language | eng | - |
dc.publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/locate/lancet | - |
dc.relation.ispartof | The Lancet | - |
dc.title | 2 years versus 1 year of adjuvant trastuzumab for HER2-positive breast cancer (HERA): an open-label, randomised controlled trial | - |
dc.type | Article | - |
dc.identifier.email | Kwong, A: avakwong@hku.hk | - |
dc.identifier.authority | Kwong, A=rp01734 | - |
dc.identifier.doi | 10.1016/S0140-6736(13)61094-6 | - |
dc.identifier.scopus | eid_2-s2.0-84884418164 | - |
dc.identifier.hkuros | 284575 | - |
dc.identifier.volume | 382 | - |
dc.identifier.issue | 9897 | - |
dc.identifier.spage | 1021 | - |
dc.identifier.epage | 1028 | - |
dc.identifier.isi | WOS:000324742200022 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.f1000 | 718043513 | - |
dc.identifier.issnl | 0140-6736 | - |