Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.

<h4>Background</h4>Hormone receptor positive breast cancer is characterized by the potential for disease recurrence many years after initial diagnosis. Endocrine therapy has been shown to reduce the risk of such recurrence, but the optimal duration of endocrine therapy remains unclear.&l...

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Main Authors: Mustafa Al-Mubarak, Ariadna Tibau, Arnoud J Templeton, David W Cescon, Alberto Ocana, Bostjan Seruga, Eitan Amir
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0088238&type=printable
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author Mustafa Al-Mubarak
Ariadna Tibau
Arnoud J Templeton
David W Cescon
Alberto Ocana
Bostjan Seruga
Eitan Amir
author_facet Mustafa Al-Mubarak
Ariadna Tibau
Arnoud J Templeton
David W Cescon
Alberto Ocana
Bostjan Seruga
Eitan Amir
author_sort Mustafa Al-Mubarak
collection DOAJ
description <h4>Background</h4>Hormone receptor positive breast cancer is characterized by the potential for disease recurrence many years after initial diagnosis. Endocrine therapy has been shown to reduce the risk of such recurrence, but the optimal duration of endocrine therapy remains unclear.<h4>Methods</h4>We conducted a systematic review and meta-analysis to quantify the benefits and harms of extended adjuvant tamoxifen (>5 years of therapy) compared with adjuvant tamoxifen (5 years of therapy). Odds ratios (ORs) and 95% confidence intervals (CIs) were computed for disease recurrence, death and adverse events. Subgroup analyses by timing of recurrence and baseline lymph node and menopause status were carried.<h4>Results</h4>Five trials comprising 21,554 patients were included. Extended adjuvant tamoxifen was not associated with a significant reduction in the risk of recurrence (OR:0.89, 95% CI 0.76-1.05, p = 0.17). There was no association between extended adjuvant tamoxifen and all-cause death (OR:0.99, 95% CI 0.84-1.16, p = 0.88). There was an apparent reduction in risk of recurrence occurring after completion of extended adjuvant tamoxifen with little evidence of effect during therapy, however, this difference was not significant (p for difference 0.10). Subgroup analysis suggested that a greater effect size among lymph node positive patients compared with those who are lymph node negative (NNT: 25 vs. 49). There was no apparent difference in the effect between pre- and post-menopausal patients. Endometrial carcinoma was substantially more frequent with extended adjuvant tamoxifen (OR:2.06, 95% CI 1.65-2.58, p<0.001, number needed to harm:89).<h4>Conclusion</h4>In unselected patients, extended adjuvant tamoxifen is not associated with a significant reduction in recurrence, or a reduction in all-cause death. Patients with lymph node positive breast cancer may derive some benefit. Reduction in the risk of recurrence appears to occur only after completion of extended adjuvant therapy.
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spelling doaj-art-ecade11c33824d7d861f06bb5caabb772025-08-20T03:01:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8823810.1371/journal.pone.0088238Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.Mustafa Al-MubarakAriadna TibauArnoud J TempletonDavid W CesconAlberto OcanaBostjan SerugaEitan Amir<h4>Background</h4>Hormone receptor positive breast cancer is characterized by the potential for disease recurrence many years after initial diagnosis. Endocrine therapy has been shown to reduce the risk of such recurrence, but the optimal duration of endocrine therapy remains unclear.<h4>Methods</h4>We conducted a systematic review and meta-analysis to quantify the benefits and harms of extended adjuvant tamoxifen (>5 years of therapy) compared with adjuvant tamoxifen (5 years of therapy). Odds ratios (ORs) and 95% confidence intervals (CIs) were computed for disease recurrence, death and adverse events. Subgroup analyses by timing of recurrence and baseline lymph node and menopause status were carried.<h4>Results</h4>Five trials comprising 21,554 patients were included. Extended adjuvant tamoxifen was not associated with a significant reduction in the risk of recurrence (OR:0.89, 95% CI 0.76-1.05, p = 0.17). There was no association between extended adjuvant tamoxifen and all-cause death (OR:0.99, 95% CI 0.84-1.16, p = 0.88). There was an apparent reduction in risk of recurrence occurring after completion of extended adjuvant tamoxifen with little evidence of effect during therapy, however, this difference was not significant (p for difference 0.10). Subgroup analysis suggested that a greater effect size among lymph node positive patients compared with those who are lymph node negative (NNT: 25 vs. 49). There was no apparent difference in the effect between pre- and post-menopausal patients. Endometrial carcinoma was substantially more frequent with extended adjuvant tamoxifen (OR:2.06, 95% CI 1.65-2.58, p<0.001, number needed to harm:89).<h4>Conclusion</h4>In unselected patients, extended adjuvant tamoxifen is not associated with a significant reduction in recurrence, or a reduction in all-cause death. Patients with lymph node positive breast cancer may derive some benefit. Reduction in the risk of recurrence appears to occur only after completion of extended adjuvant therapy.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0088238&type=printable
spellingShingle Mustafa Al-Mubarak
Ariadna Tibau
Arnoud J Templeton
David W Cescon
Alberto Ocana
Bostjan Seruga
Eitan Amir
Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.
PLoS ONE
title Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.
title_full Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.
title_fullStr Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.
title_full_unstemmed Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.
title_short Extended adjuvant tamoxifen for early breast cancer: a meta-analysis.
title_sort extended adjuvant tamoxifen for early breast cancer a meta analysis
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0088238&type=printable
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AT albertoocana extendedadjuvanttamoxifenforearlybreastcancerametaanalysis
AT bostjanseruga extendedadjuvanttamoxifenforearlybreastcancerametaanalysis
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