Estimating the magnitude of trastuzumab effects within patient subgroups in the HERA trial
Untch, M., Gelber, R. D., Jackisch, C., Procter, M., Baselga, J., Bell, R., Cameron, D., Bari, M., Smith, I., Leyland-Jones, B., de Azambuja, E., Wermuth, P., Khasanov, R., Feng-yi, F., Constantin, C., Mayordomo, J. I., Su, C. H., Yu, S. Y., Lluch, A., Senkus-Konefka, E., Price, C., Haslbauer, F., Sahui, T. S., Srimuninnimit, V., Colleoni, M., Coates, A. S., Piccart-Gebhart, M. J., Goldhirsch, A., HERA Study Team, [Group Author]
(2008)
Estimating the magnitude of trastuzumab effects within patient subgroups in the HERA trial.
ANNALS OF ONCOLOGY, 19 (6).
pp. 1090-1096.
ISSN 0923-7534
Full text not available from this repository.
Abstract
Background: Trastuzumab (Herceptin (R)) improves disease-free survival (DFS) and overall survival for patients with human epidermal growth factor receptor 2 (HER2)-positive early breast cancer. We aimed to assess the magnitude of its clinical benefit for subpopulations defined by nodal and steroid hormone receptor status using data from the Herceptin Adjuvant (HERA) study. Patients and methods: HERA is an international multicenter randomized trial comparing 1 or 2 years of trastuzumab treatment with observation after standard chemotherapy in women with HER2-positive breast cancer. In total, 1703 women randomized to 1-year trastuzumab and 1698 women randomized to observation were included in these analyses. Median follow-up was 23.5 months. The primary endpoint was DFS. Results: The overall hazard ratio (HR) for trastuzumab versus observation was 0.64 [95% confidence interval (CI) 0.54-0.76; P < 0.0001], ranging from 0.46 to 0.82 for subgroups. Estimated improvement in 3-year DFS in subgroups ranged from +11.3% to +0.6%. Patients with the best prognosis (those with node-negative disease and tumors 1.1-2.0 cm) had benefit similar to the overall cohort (HR 0.53, 95% CI 0.26-1.07; 3-year DFS improvement +4.6%, 95% CI -4.0% to 13.2%). Conclusions: Adjuvant trastuzumab therapy reduces the risk of relapse similarly across subgroups defined by nodal status and steroid hormone receptor status, even those at relatively low risk for relapse.
Item Type: | Article |
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Authors (ICR Faculty only): | Smith, Ian |
All Authors: | Untch, M., Gelber, R. D., Jackisch, C., Procter, M., Baselga, J., Bell, R., Cameron, D., Bari, M., Smith, I., Leyland-Jones, B., de Azambuja, E., Wermuth, P., Khasanov, R., Feng-yi, F., Constantin, C., Mayordomo, J. I., Su, C. H., Yu, S. Y., Lluch, A., Senkus-Konefka, E., Price, C., Haslbauer, F., Sahui, T. S., Srimuninnimit, V., Colleoni, M., Coates, A. S., Piccart-Gebhart, M. J., Goldhirsch, A., HERA Study Team, [Group Author] |
Uncontrolled Keywords: | adjuvant therapy; breast cancer; disease-free survival; HER2-oncogene; subgroubs; trastuzumab HER2-POSITIVE BREAST-CANCER; ADJUVANT CHEMOTHERAPY |
Research teams: | Clinical Units > Breast Unit |
Depositing User: | Users 10 not found. |
Date Deposited: | 17 Jun 2008 12:17 |
Last Modified: | 13 Nov 2009 04:13 |
URI: | http://publications.icr.ac.uk/id/eprint/6461 |
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