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Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark

Evidence regarding cancer risk after borderline ovarian tumors (BOTs) is limited. We conducted a nationwide cohort study examining the incidence of nonovarian cancers in women with serous or mucinous BOTs compared with the general female population with up to 41 years of follow‐up. Through the natio...

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Autores principales: Hannibal, Charlotte G., Baandrup, Louise, Hertzum‐Larsen, Rasmus, Vang, Russell, Kurman, Robert J., Frederiksen, Kirsten, Kjaer, Susanne Krüger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099848/
https://www.ncbi.nlm.nih.gov/pubmed/36366853
http://dx.doi.org/10.1002/ijc.34354
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author Hannibal, Charlotte G.
Baandrup, Louise
Hertzum‐Larsen, Rasmus
Vang, Russell
Kurman, Robert J.
Frederiksen, Kirsten
Kjaer, Susanne Krüger
author_facet Hannibal, Charlotte G.
Baandrup, Louise
Hertzum‐Larsen, Rasmus
Vang, Russell
Kurman, Robert J.
Frederiksen, Kirsten
Kjaer, Susanne Krüger
author_sort Hannibal, Charlotte G.
collection PubMed
description Evidence regarding cancer risk after borderline ovarian tumors (BOTs) is limited. We conducted a nationwide cohort study examining the incidence of nonovarian cancers in women with serous or mucinous BOTs compared with the general female population with up to 41 years of follow‐up. Through the nationwide Pathology Registry, we identified nearly 5000 women with BOTs (2506 serous and 2493 mucinous) in Denmark, 1978 to 2018. We computed standardized incidence ratios (SIRs) with 95% confidence intervals (CIs) as relative risk estimates of specific nonovarian cancers. Compared with general female population rates, women with serous BOTs had increased rates of particularly malignant melanoma (SIR = 1.9; 95% CI: 1.3‐2.6), thyroid cancer (SIR = 3.0; 95% CI: 1.4‐5.4) and myeloid leukemia (SIR = 3.2; 95% CI: 1.5‐5.8), and women with mucinous BOTs had elevated rates of lung cancer (SIR = 1.7; 95% CI: 1.3‐2.1), pancreatic cancer (SIR = 1.9; 95% CI: 1.2‐2.9) and myeloid leukemia (SIR = 2.3; 95% CI: 0.9‐4.7). We found no convincing association with neither breast nor colorectal cancer in women with BOTs. This is the first large nationwide study showing that women with specific types of BOTs have increased risks of several nonovarian cancers, likely due to some shared risk factors or genetic characteristics.
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spelling pubmed-100998482023-04-14 Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark Hannibal, Charlotte G. Baandrup, Louise Hertzum‐Larsen, Rasmus Vang, Russell Kurman, Robert J. Frederiksen, Kirsten Kjaer, Susanne Krüger Int J Cancer Cancer Epidemiology Evidence regarding cancer risk after borderline ovarian tumors (BOTs) is limited. We conducted a nationwide cohort study examining the incidence of nonovarian cancers in women with serous or mucinous BOTs compared with the general female population with up to 41 years of follow‐up. Through the nationwide Pathology Registry, we identified nearly 5000 women with BOTs (2506 serous and 2493 mucinous) in Denmark, 1978 to 2018. We computed standardized incidence ratios (SIRs) with 95% confidence intervals (CIs) as relative risk estimates of specific nonovarian cancers. Compared with general female population rates, women with serous BOTs had increased rates of particularly malignant melanoma (SIR = 1.9; 95% CI: 1.3‐2.6), thyroid cancer (SIR = 3.0; 95% CI: 1.4‐5.4) and myeloid leukemia (SIR = 3.2; 95% CI: 1.5‐5.8), and women with mucinous BOTs had elevated rates of lung cancer (SIR = 1.7; 95% CI: 1.3‐2.1), pancreatic cancer (SIR = 1.9; 95% CI: 1.2‐2.9) and myeloid leukemia (SIR = 2.3; 95% CI: 0.9‐4.7). We found no convincing association with neither breast nor colorectal cancer in women with BOTs. This is the first large nationwide study showing that women with specific types of BOTs have increased risks of several nonovarian cancers, likely due to some shared risk factors or genetic characteristics. John Wiley & Sons, Inc. 2022-11-23 2023-04-01 /pmc/articles/PMC10099848/ /pubmed/36366853 http://dx.doi.org/10.1002/ijc.34354 Text en © 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cancer Epidemiology
Hannibal, Charlotte G.
Baandrup, Louise
Hertzum‐Larsen, Rasmus
Vang, Russell
Kurman, Robert J.
Frederiksen, Kirsten
Kjaer, Susanne Krüger
Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark
title Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark
title_full Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark
title_fullStr Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark
title_full_unstemmed Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark
title_short Risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in Denmark
title_sort risk of nonovarian cancer in a nationwide‐based study of nearly 5000 women with borderline ovarian tumors in denmark
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099848/
https://www.ncbi.nlm.nih.gov/pubmed/36366853
http://dx.doi.org/10.1002/ijc.34354
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