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Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial
BACKGROUND: The DATA study evaluated the use of two different durations of anastrozole in patients with hormone receptor-positive breast cancer who were disease-free after 2–3 years of tamoxifen. We hereby present the follow-up analysis, which was performed after all patients reached a minimum follo...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041456/ https://www.ncbi.nlm.nih.gov/pubmed/36992863 http://dx.doi.org/10.1016/j.eclinm.2023.101901 |
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author | Tjan-Heijnen, Vivianne C.G. Lammers, Senna W.M. Geurts, Sandra M.E. Vriens, Ingeborg J.H. Swinkels, Astrid C.P. Smorenburg, Carolien H. van der Sangen, Maurice J.C. Kroep, Judith R. de Graaf, Hiltje Honkoop, Aafke H. Erdkamp, Frans L.G. de Roos, Wilfred K. Linn, Sabine C. Imholz, Alexander L.T. |
author_facet | Tjan-Heijnen, Vivianne C.G. Lammers, Senna W.M. Geurts, Sandra M.E. Vriens, Ingeborg J.H. Swinkels, Astrid C.P. Smorenburg, Carolien H. van der Sangen, Maurice J.C. Kroep, Judith R. de Graaf, Hiltje Honkoop, Aafke H. Erdkamp, Frans L.G. de Roos, Wilfred K. Linn, Sabine C. Imholz, Alexander L.T. |
author_sort | Tjan-Heijnen, Vivianne C.G. |
collection | PubMed |
description | BACKGROUND: The DATA study evaluated the use of two different durations of anastrozole in patients with hormone receptor-positive breast cancer who were disease-free after 2–3 years of tamoxifen. We hereby present the follow-up analysis, which was performed after all patients reached a minimum follow-up of 10 years beyond treatment divergence. METHODS: The open-label, randomised, phase 3 DATA study was performed in 79 hospitals in the Netherlands (ClinicalTrials.gov, number NCT00301457). Postmenopausal women with hormone receptor-positive breast cancer who were disease-free after 2–3 years of adjuvant tamoxifen treatment were assigned to either 3 or 6 years of anastrozole (1 mg orally once a day). Randomisation (1:1) was stratified by hormone receptor status, nodal status, HER2 status, and prior tamoxifen duration. The primary outcome was adapted disease-free survival, defined as disease-free survival from 3 years after randomisation onwards. Adapted overall survival was assessed as a secondary outcome. Analyses were performed according to the intention-to-treat design. FINDINGS: Between June 28, 2006, and August 10, 2009, 1912 patients were randomly assigned to 3 years (n = 955) or 6 years (n = 957) of anastrozole. Of these, 1660 patients were eligible and disease-free at 3 years after randomisation. The 10-year adapted disease-free survival was 69.2% (95% CI 55.8–72.3) in the 6-year group (n = 827) and 66.0% (95% CI 62.5–69.2) in the 3-year group (n = 833) (hazard ratio (HR) 0.86; 95% CI 0.72–1.01; p = 0.073). The 10-year adapted overall survival was 80.9% (95% CI 77.9–83.5) in the 6-year group and 79.2% (95% CI 76.2–81.9) in the 3-year group (HR 0.93; 95% CI 0.75–1.16; p = 0.53). INTERPRETATION: Extended aromatase inhibition beyond 5 years of sequential endocrine therapy did not improve the adapted disease-free survival and adapted overall survival of postmenopausal women with hormone receptor-positive breast cancer. FUNDING: AstraZeneca. |
format | Online Article Text |
id | pubmed-10041456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100414562023-03-28 Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial Tjan-Heijnen, Vivianne C.G. Lammers, Senna W.M. Geurts, Sandra M.E. Vriens, Ingeborg J.H. Swinkels, Astrid C.P. Smorenburg, Carolien H. van der Sangen, Maurice J.C. Kroep, Judith R. de Graaf, Hiltje Honkoop, Aafke H. Erdkamp, Frans L.G. de Roos, Wilfred K. Linn, Sabine C. Imholz, Alexander L.T. eClinicalMedicine Articles BACKGROUND: The DATA study evaluated the use of two different durations of anastrozole in patients with hormone receptor-positive breast cancer who were disease-free after 2–3 years of tamoxifen. We hereby present the follow-up analysis, which was performed after all patients reached a minimum follow-up of 10 years beyond treatment divergence. METHODS: The open-label, randomised, phase 3 DATA study was performed in 79 hospitals in the Netherlands (ClinicalTrials.gov, number NCT00301457). Postmenopausal women with hormone receptor-positive breast cancer who were disease-free after 2–3 years of adjuvant tamoxifen treatment were assigned to either 3 or 6 years of anastrozole (1 mg orally once a day). Randomisation (1:1) was stratified by hormone receptor status, nodal status, HER2 status, and prior tamoxifen duration. The primary outcome was adapted disease-free survival, defined as disease-free survival from 3 years after randomisation onwards. Adapted overall survival was assessed as a secondary outcome. Analyses were performed according to the intention-to-treat design. FINDINGS: Between June 28, 2006, and August 10, 2009, 1912 patients were randomly assigned to 3 years (n = 955) or 6 years (n = 957) of anastrozole. Of these, 1660 patients were eligible and disease-free at 3 years after randomisation. The 10-year adapted disease-free survival was 69.2% (95% CI 55.8–72.3) in the 6-year group (n = 827) and 66.0% (95% CI 62.5–69.2) in the 3-year group (n = 833) (hazard ratio (HR) 0.86; 95% CI 0.72–1.01; p = 0.073). The 10-year adapted overall survival was 80.9% (95% CI 77.9–83.5) in the 6-year group and 79.2% (95% CI 76.2–81.9) in the 3-year group (HR 0.93; 95% CI 0.75–1.16; p = 0.53). INTERPRETATION: Extended aromatase inhibition beyond 5 years of sequential endocrine therapy did not improve the adapted disease-free survival and adapted overall survival of postmenopausal women with hormone receptor-positive breast cancer. FUNDING: AstraZeneca. Elsevier 2023-03-20 /pmc/articles/PMC10041456/ /pubmed/36992863 http://dx.doi.org/10.1016/j.eclinm.2023.101901 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Articles Tjan-Heijnen, Vivianne C.G. Lammers, Senna W.M. Geurts, Sandra M.E. Vriens, Ingeborg J.H. Swinkels, Astrid C.P. Smorenburg, Carolien H. van der Sangen, Maurice J.C. Kroep, Judith R. de Graaf, Hiltje Honkoop, Aafke H. Erdkamp, Frans L.G. de Roos, Wilfred K. Linn, Sabine C. Imholz, Alexander L.T. Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial |
title | Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial |
title_full | Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial |
title_fullStr | Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial |
title_full_unstemmed | Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial |
title_short | Extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 DATA trial |
title_sort | extended adjuvant aromatase inhibition after sequential endocrine therapy in postmenopausal women with breast cancer: follow-up analysis of the randomised phase 3 data trial |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041456/ https://www.ncbi.nlm.nih.gov/pubmed/36992863 http://dx.doi.org/10.1016/j.eclinm.2023.101901 |
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