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Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study

BACKGROUND: Although menopausal hormone therapy (MHT) use has been linked with an increased risk of ovarian cancer, whether pre-diagnosis MHT use affects ovarian cancer-specific mortality is unknown. METHODS: Our analysis included 395 incident epithelial ovarian cancer patients with data on pre-diag...

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Autores principales: Felix, Ashley S., Bunch, Kristen, Yang, Hannah P., Arem, Hannah, Trabert, Britton, Gierach, Gretchen L., Park, Yikyung, Lowery, William J., Brinton, Louise A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563575/
https://www.ncbi.nlm.nih.gov/pubmed/26425711
http://dx.doi.org/10.1016/j.gore.2015.04.007
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author Felix, Ashley S.
Bunch, Kristen
Yang, Hannah P.
Arem, Hannah
Trabert, Britton
Gierach, Gretchen L.
Park, Yikyung
Lowery, William J.
Brinton, Louise A.
author_facet Felix, Ashley S.
Bunch, Kristen
Yang, Hannah P.
Arem, Hannah
Trabert, Britton
Gierach, Gretchen L.
Park, Yikyung
Lowery, William J.
Brinton, Louise A.
author_sort Felix, Ashley S.
collection PubMed
description BACKGROUND: Although menopausal hormone therapy (MHT) use has been linked with an increased risk of ovarian cancer, whether pre-diagnosis MHT use affects ovarian cancer-specific mortality is unknown. METHODS: Our analysis included 395 incident epithelial ovarian cancer patients with data on pre-diagnosis MHT use from the National Institutes of Health-AARP (NIH-AARP) Diet and Health Study. We used Cox proportional hazards regression models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for MHT type and ovarian cancer-specific mortality, adjusted for tumor characteristics, treatment, and other risk factors. Effect modification by histology (serous vs. non-serous) was examined using likelihood ratio tests comparing models with and without interaction terms between MHT type and histology. RESULTS: Ovarian cancer-specific mortality was not associated with pre-diagnosis estrogen-only therapy (ET) (HR = 1.09, 95% CI = 0.70–1.68) or estrogen plus progestin-only therapy (EPT) (HR = 0.97, 95% CI = 0.68–1.38). Neither recency of use nor specific regimen of EPT-only (sequential vs. continuous) was related to mortality. In analyses stratified by histology, no significant association between MHT type and ovarian cancer-specific mortality was observed among serous or non-serous cases; however, a significant interaction between MHT type and histology was noted (p-heterogeneity = 0.01). CONCLUSION: Our results suggest that pre-diagnosis MHT use is not related to risk of ovarian cancer-specific death.
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spelling pubmed-45635752015-09-30 Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study Felix, Ashley S. Bunch, Kristen Yang, Hannah P. Arem, Hannah Trabert, Britton Gierach, Gretchen L. Park, Yikyung Lowery, William J. Brinton, Louise A. Gynecol Oncol Rep Case Series BACKGROUND: Although menopausal hormone therapy (MHT) use has been linked with an increased risk of ovarian cancer, whether pre-diagnosis MHT use affects ovarian cancer-specific mortality is unknown. METHODS: Our analysis included 395 incident epithelial ovarian cancer patients with data on pre-diagnosis MHT use from the National Institutes of Health-AARP (NIH-AARP) Diet and Health Study. We used Cox proportional hazards regression models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for MHT type and ovarian cancer-specific mortality, adjusted for tumor characteristics, treatment, and other risk factors. Effect modification by histology (serous vs. non-serous) was examined using likelihood ratio tests comparing models with and without interaction terms between MHT type and histology. RESULTS: Ovarian cancer-specific mortality was not associated with pre-diagnosis estrogen-only therapy (ET) (HR = 1.09, 95% CI = 0.70–1.68) or estrogen plus progestin-only therapy (EPT) (HR = 0.97, 95% CI = 0.68–1.38). Neither recency of use nor specific regimen of EPT-only (sequential vs. continuous) was related to mortality. In analyses stratified by histology, no significant association between MHT type and ovarian cancer-specific mortality was observed among serous or non-serous cases; however, a significant interaction between MHT type and histology was noted (p-heterogeneity = 0.01). CONCLUSION: Our results suggest that pre-diagnosis MHT use is not related to risk of ovarian cancer-specific death. Elsevier 2015-05-08 /pmc/articles/PMC4563575/ /pubmed/26425711 http://dx.doi.org/10.1016/j.gore.2015.04.007 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Series
Felix, Ashley S.
Bunch, Kristen
Yang, Hannah P.
Arem, Hannah
Trabert, Britton
Gierach, Gretchen L.
Park, Yikyung
Lowery, William J.
Brinton, Louise A.
Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study
title Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study
title_full Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study
title_fullStr Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study
title_full_unstemmed Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study
title_short Menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the NIH-AARP Diet and Health Study
title_sort menopausal hormone therapy and mortality among women diagnosed with ovarian cancer in the nih-aarp diet and health study
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563575/
https://www.ncbi.nlm.nih.gov/pubmed/26425711
http://dx.doi.org/10.1016/j.gore.2015.04.007
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