Parity, infertility, oral contraceptives, and hormone replacement therapy and the risk of ovarian serous borderline tumors: A nationwide case-control study

Abstract Objective Few studies have examined the risk of an ovarian serous borderline tumor (SBT) associated with parity, infertility, oral contraceptives (OCs), or hormone replacement therapy (HRT), which was the study aim. Methods This nationwide case-control study included all women with an SBT d...

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Veröffentlicht in:Gynecologic oncology 2017-03, Vol.144 (3), p.571-576
Hauptverfasser: Rasmussen, Emma L. Kaderly, Hannibal, Charlotte Gerd, Dehlendorff, Christian, Baandrup, Louise, Junge, Jette, Vang, Russell, Kurman, Robert J, Kjaer, Susanne K
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container_end_page 576
container_issue 3
container_start_page 571
container_title Gynecologic oncology
container_volume 144
creator Rasmussen, Emma L. Kaderly
Hannibal, Charlotte Gerd
Dehlendorff, Christian
Baandrup, Louise
Junge, Jette
Vang, Russell
Kurman, Robert J
Kjaer, Susanne K
description Abstract Objective Few studies have examined the risk of an ovarian serous borderline tumor (SBT) associated with parity, infertility, oral contraceptives (OCs), or hormone replacement therapy (HRT), which was the study aim. Methods This nationwide case-control study included all women with an SBT diagnosis in Denmark, 1978–2002. SBTs were confirmed by centralized expert pathology review. For each case, 15 age-matched female controls were randomly selected using risk-set sampling. Cases and controls with previous cancer (except for non-melanoma skin cancer) and controls with bilateral oophorectomy or salpingo-oophorectomy were excluded. Conditional logistic regression was used to estimate adjusted odds ratios (ORs) and 95% confidence intervals (CIs). Results We found a strongly decreased risk of SBTs among parous women which decreased with increasing number of children ( p < 0.01). Older age at first birth also decreased the SBT risk ( p = 0.03). An increased SBT risk was associated with infertility (OR = 3.31; 95% CI: 2.44–4.49), which was present both among parous and nulliparous women. HRT use increased the SBT risk (OR = 1.32; 95% CI: 1.02–1.72), whereas OC use decreased the risk (OR = 0.40; 95% CI: 0.26–0.62). Conclusions Our nationwide study with expert histopathologic review of all SBTs showed that parity, infertility, use of HRT, and use of OCs, respectively, were strongly associated with the risk of SBTs. This is the first study to report a strong and significantly decreased SBT risk associated with OC use and a significantly increased risk with infertility, and HRT use. This supports that SBTs and serous ovarian cancer share similar risk factors.
doi_str_mv 10.1016/j.ygyno.2017.01.002
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Kaderly ; Hannibal, Charlotte Gerd ; Dehlendorff, Christian ; Baandrup, Louise ; Junge, Jette ; Vang, Russell ; Kurman, Robert J ; Kjaer, Susanne K</creator><creatorcontrib>Rasmussen, Emma L. Kaderly ; Hannibal, Charlotte Gerd ; Dehlendorff, Christian ; Baandrup, Louise ; Junge, Jette ; Vang, Russell ; Kurman, Robert J ; Kjaer, Susanne K</creatorcontrib><description>Abstract Objective Few studies have examined the risk of an ovarian serous borderline tumor (SBT) associated with parity, infertility, oral contraceptives (OCs), or hormone replacement therapy (HRT), which was the study aim. Methods This nationwide case-control study included all women with an SBT diagnosis in Denmark, 1978–2002. SBTs were confirmed by centralized expert pathology review. For each case, 15 age-matched female controls were randomly selected using risk-set sampling. Cases and controls with previous cancer (except for non-melanoma skin cancer) and controls with bilateral oophorectomy or salpingo-oophorectomy were excluded. Conditional logistic regression was used to estimate adjusted odds ratios (ORs) and 95% confidence intervals (CIs). Results We found a strongly decreased risk of SBTs among parous women which decreased with increasing number of children ( p &lt; 0.01). Older age at first birth also decreased the SBT risk ( p = 0.03). An increased SBT risk was associated with infertility (OR = 3.31; 95% CI: 2.44–4.49), which was present both among parous and nulliparous women. HRT use increased the SBT risk (OR = 1.32; 95% CI: 1.02–1.72), whereas OC use decreased the risk (OR = 0.40; 95% CI: 0.26–0.62). Conclusions Our nationwide study with expert histopathologic review of all SBTs showed that parity, infertility, use of HRT, and use of OCs, respectively, were strongly associated with the risk of SBTs. This is the first study to report a strong and significantly decreased SBT risk associated with OC use and a significantly increased risk with infertility, and HRT use. This supports that SBTs and serous ovarian cancer share similar risk factors.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2017.01.002</identifier><identifier>PMID: 28108026</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Carcinoma, Ovarian Epithelial ; Case-Control Studies ; Contraceptives, Oral - administration &amp; dosage ; Cystadenocarcinoma, Serous - diagnosis ; Cystadenocarcinoma, Serous - epidemiology ; Denmark - epidemiology ; Female ; Hematology, Oncology and Palliative Medicine ; Hormone replacement therapy (HRT) ; Hormone Replacement Therapy - statistics &amp; numerical data ; Humans ; Infertility ; Infertility - epidemiology ; Neoplasms, Glandular and Epithelial - diagnosis ; Neoplasms, Glandular and Epithelial - epidemiology ; Obstetrics and Gynecology ; Oral contraceptive (OC) ; Ovarian Neoplasms - diagnosis ; Ovarian Neoplasms - epidemiology ; Ovarian serous borderline tumor (SBT) ; Parity ; Risk factor ; Risk Factors ; Young Adult</subject><ispartof>Gynecologic oncology, 2017-03, Vol.144 (3), p.571-576</ispartof><rights>Elsevier Inc.</rights><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-2224b9eab2905c2a16dfa5e65cf74886971eca2dad45b4f2e823f630d4f0d9f53</citedby><cites>FETCH-LOGICAL-c414t-2224b9eab2905c2a16dfa5e65cf74886971eca2dad45b4f2e823f630d4f0d9f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ygyno.2017.01.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28108026$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rasmussen, Emma L. Kaderly</creatorcontrib><creatorcontrib>Hannibal, Charlotte Gerd</creatorcontrib><creatorcontrib>Dehlendorff, Christian</creatorcontrib><creatorcontrib>Baandrup, Louise</creatorcontrib><creatorcontrib>Junge, Jette</creatorcontrib><creatorcontrib>Vang, Russell</creatorcontrib><creatorcontrib>Kurman, Robert J</creatorcontrib><creatorcontrib>Kjaer, Susanne K</creatorcontrib><title>Parity, infertility, oral contraceptives, and hormone replacement therapy and the risk of ovarian serous borderline tumors: A nationwide case-control study</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Abstract Objective Few studies have examined the risk of an ovarian serous borderline tumor (SBT) associated with parity, infertility, oral contraceptives (OCs), or hormone replacement therapy (HRT), which was the study aim. Methods This nationwide case-control study included all women with an SBT diagnosis in Denmark, 1978–2002. SBTs were confirmed by centralized expert pathology review. For each case, 15 age-matched female controls were randomly selected using risk-set sampling. Cases and controls with previous cancer (except for non-melanoma skin cancer) and controls with bilateral oophorectomy or salpingo-oophorectomy were excluded. Conditional logistic regression was used to estimate adjusted odds ratios (ORs) and 95% confidence intervals (CIs). Results We found a strongly decreased risk of SBTs among parous women which decreased with increasing number of children ( p &lt; 0.01). Older age at first birth also decreased the SBT risk ( p = 0.03). An increased SBT risk was associated with infertility (OR = 3.31; 95% CI: 2.44–4.49), which was present both among parous and nulliparous women. HRT use increased the SBT risk (OR = 1.32; 95% CI: 1.02–1.72), whereas OC use decreased the risk (OR = 0.40; 95% CI: 0.26–0.62). Conclusions Our nationwide study with expert histopathologic review of all SBTs showed that parity, infertility, use of HRT, and use of OCs, respectively, were strongly associated with the risk of SBTs. This is the first study to report a strong and significantly decreased SBT risk associated with OC use and a significantly increased risk with infertility, and HRT use. 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Kaderly</creator><creator>Hannibal, Charlotte Gerd</creator><creator>Dehlendorff, Christian</creator><creator>Baandrup, Louise</creator><creator>Junge, Jette</creator><creator>Vang, Russell</creator><creator>Kurman, Robert J</creator><creator>Kjaer, Susanne K</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170301</creationdate><title>Parity, infertility, oral contraceptives, and hormone replacement therapy and the risk of ovarian serous borderline tumors: A nationwide case-control study</title><author>Rasmussen, Emma L. 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Kaderly</creatorcontrib><creatorcontrib>Hannibal, Charlotte Gerd</creatorcontrib><creatorcontrib>Dehlendorff, Christian</creatorcontrib><creatorcontrib>Baandrup, Louise</creatorcontrib><creatorcontrib>Junge, Jette</creatorcontrib><creatorcontrib>Vang, Russell</creatorcontrib><creatorcontrib>Kurman, Robert J</creatorcontrib><creatorcontrib>Kjaer, Susanne K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rasmussen, Emma L. Kaderly</au><au>Hannibal, Charlotte Gerd</au><au>Dehlendorff, Christian</au><au>Baandrup, Louise</au><au>Junge, Jette</au><au>Vang, Russell</au><au>Kurman, Robert J</au><au>Kjaer, Susanne K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parity, infertility, oral contraceptives, and hormone replacement therapy and the risk of ovarian serous borderline tumors: A nationwide case-control study</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>144</volume><issue>3</issue><spage>571</spage><epage>576</epage><pages>571-576</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>Abstract Objective Few studies have examined the risk of an ovarian serous borderline tumor (SBT) associated with parity, infertility, oral contraceptives (OCs), or hormone replacement therapy (HRT), which was the study aim. Methods This nationwide case-control study included all women with an SBT diagnosis in Denmark, 1978–2002. SBTs were confirmed by centralized expert pathology review. For each case, 15 age-matched female controls were randomly selected using risk-set sampling. Cases and controls with previous cancer (except for non-melanoma skin cancer) and controls with bilateral oophorectomy or salpingo-oophorectomy were excluded. Conditional logistic regression was used to estimate adjusted odds ratios (ORs) and 95% confidence intervals (CIs). Results We found a strongly decreased risk of SBTs among parous women which decreased with increasing number of children ( p &lt; 0.01). Older age at first birth also decreased the SBT risk ( p = 0.03). An increased SBT risk was associated with infertility (OR = 3.31; 95% CI: 2.44–4.49), which was present both among parous and nulliparous women. HRT use increased the SBT risk (OR = 1.32; 95% CI: 1.02–1.72), whereas OC use decreased the risk (OR = 0.40; 95% CI: 0.26–0.62). Conclusions Our nationwide study with expert histopathologic review of all SBTs showed that parity, infertility, use of HRT, and use of OCs, respectively, were strongly associated with the risk of SBTs. This is the first study to report a strong and significantly decreased SBT risk associated with OC use and a significantly increased risk with infertility, and HRT use. This supports that SBTs and serous ovarian cancer share similar risk factors.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28108026</pmid><doi>10.1016/j.ygyno.2017.01.002</doi><tpages>6</tpages></addata></record>
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subjects Adult
Carcinoma, Ovarian Epithelial
Case-Control Studies
Contraceptives, Oral - administration & dosage
Cystadenocarcinoma, Serous - diagnosis
Cystadenocarcinoma, Serous - epidemiology
Denmark - epidemiology
Female
Hematology, Oncology and Palliative Medicine
Hormone replacement therapy (HRT)
Hormone Replacement Therapy - statistics & numerical data
Humans
Infertility
Infertility - epidemiology
Neoplasms, Glandular and Epithelial - diagnosis
Neoplasms, Glandular and Epithelial - epidemiology
Obstetrics and Gynecology
Oral contraceptive (OC)
Ovarian Neoplasms - diagnosis
Ovarian Neoplasms - epidemiology
Ovarian serous borderline tumor (SBT)
Parity
Risk factor
Risk Factors
Young Adult
title Parity, infertility, oral contraceptives, and hormone replacement therapy and the risk of ovarian serous borderline tumors: A nationwide case-control study
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