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Tamoxifen use and acute pancreatitis: A population-based cohort study

BACKGROUND: Several case reports have indicated that tamoxifen induced acute pancreatitis (AP); but no pharmacoepidemiological data support the claim. Therefore, we investigated whether tamoxifen use is correlated with the risk of AP in patients with breast cancer. METHODS: This population-based coh...

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Autores principales: Hsu, Fan-Gen, Hsieh, Yow-Wen, Sheu, Ming-Jyh, Lin, Che-Chen, Lin, Cheng-Li, Hsu, Chung Y., Lee, Chang-Yin, Chang, Mei-Yin, Chang, Kuang-Hsi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349648/
https://www.ncbi.nlm.nih.gov/pubmed/28291833
http://dx.doi.org/10.1371/journal.pone.0173089
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author Hsu, Fan-Gen
Hsieh, Yow-Wen
Sheu, Ming-Jyh
Lin, Che-Chen
Lin, Cheng-Li
Hsu, Chung Y.
Lee, Chang-Yin
Chang, Mei-Yin
Chang, Kuang-Hsi
author_facet Hsu, Fan-Gen
Hsieh, Yow-Wen
Sheu, Ming-Jyh
Lin, Che-Chen
Lin, Cheng-Li
Hsu, Chung Y.
Lee, Chang-Yin
Chang, Mei-Yin
Chang, Kuang-Hsi
author_sort Hsu, Fan-Gen
collection PubMed
description BACKGROUND: Several case reports have indicated that tamoxifen induced acute pancreatitis (AP); but no pharmacoepidemiological data support the claim. Therefore, we investigated whether tamoxifen use is correlated with the risk of AP in patients with breast cancer. METHODS: This population-based cohort study used the Taiwan National Health Insurance Research Database. A cohort of 22 005 patients aged ≥20 years with breast cancer from January 1, 2000 to December 31, 2009 was identified and the date of cancer diagnosis was set as the index date. The end point was developing AP during the follow-up. Hazard ratios (HRs) and 95% confidence intervals (CIs) were evaluated to determine the correlation between the risk of AP and tamoxifen use. Because the drug use varied over time, it was measured as a time-dependent covariate in the Cox proportional hazard model. The same approaches were applied in PS-matched cohorts. RESULTS: After adjustment for covariates and medication use including fluorouracil and doxorubicin, the risk of AP was not significant between tamoxifen users and tamoxifen nonusers (adjusted HR = 0.94, 95% CI = 0.74–1.19) in the non-matching cohorts. The results revealed no dose–response trend between tamoxifen use and the risk of AP (adjusted HR = 0.98, 95% CI = 0.96–1.00). The comorbidities DM and gallstones were associated with a significantly increased risk of AP. Similar trends were observed in PS-matched cohorts. CONCLUSIONS: No significant correlation was observed between tamoxifen use and the risk of AP in patients with breast cancer.
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spelling pubmed-53496482017-04-06 Tamoxifen use and acute pancreatitis: A population-based cohort study Hsu, Fan-Gen Hsieh, Yow-Wen Sheu, Ming-Jyh Lin, Che-Chen Lin, Cheng-Li Hsu, Chung Y. Lee, Chang-Yin Chang, Mei-Yin Chang, Kuang-Hsi PLoS One Research Article BACKGROUND: Several case reports have indicated that tamoxifen induced acute pancreatitis (AP); but no pharmacoepidemiological data support the claim. Therefore, we investigated whether tamoxifen use is correlated with the risk of AP in patients with breast cancer. METHODS: This population-based cohort study used the Taiwan National Health Insurance Research Database. A cohort of 22 005 patients aged ≥20 years with breast cancer from January 1, 2000 to December 31, 2009 was identified and the date of cancer diagnosis was set as the index date. The end point was developing AP during the follow-up. Hazard ratios (HRs) and 95% confidence intervals (CIs) were evaluated to determine the correlation between the risk of AP and tamoxifen use. Because the drug use varied over time, it was measured as a time-dependent covariate in the Cox proportional hazard model. The same approaches were applied in PS-matched cohorts. RESULTS: After adjustment for covariates and medication use including fluorouracil and doxorubicin, the risk of AP was not significant between tamoxifen users and tamoxifen nonusers (adjusted HR = 0.94, 95% CI = 0.74–1.19) in the non-matching cohorts. The results revealed no dose–response trend between tamoxifen use and the risk of AP (adjusted HR = 0.98, 95% CI = 0.96–1.00). The comorbidities DM and gallstones were associated with a significantly increased risk of AP. Similar trends were observed in PS-matched cohorts. CONCLUSIONS: No significant correlation was observed between tamoxifen use and the risk of AP in patients with breast cancer. Public Library of Science 2017-03-14 /pmc/articles/PMC5349648/ /pubmed/28291833 http://dx.doi.org/10.1371/journal.pone.0173089 Text en © 2017 Hsu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hsu, Fan-Gen
Hsieh, Yow-Wen
Sheu, Ming-Jyh
Lin, Che-Chen
Lin, Cheng-Li
Hsu, Chung Y.
Lee, Chang-Yin
Chang, Mei-Yin
Chang, Kuang-Hsi
Tamoxifen use and acute pancreatitis: A population-based cohort study
title Tamoxifen use and acute pancreatitis: A population-based cohort study
title_full Tamoxifen use and acute pancreatitis: A population-based cohort study
title_fullStr Tamoxifen use and acute pancreatitis: A population-based cohort study
title_full_unstemmed Tamoxifen use and acute pancreatitis: A population-based cohort study
title_short Tamoxifen use and acute pancreatitis: A population-based cohort study
title_sort tamoxifen use and acute pancreatitis: a population-based cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349648/
https://www.ncbi.nlm.nih.gov/pubmed/28291833
http://dx.doi.org/10.1371/journal.pone.0173089
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