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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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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. |
format | Online Article Text |
id | pubmed-5349648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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