The timing of venous thromboembolism in ovarian cancer patients: A nationwide Danish cohort study

Background and aim Venous thromboembolism (VTE) is associated with excess mortality and morbidity in cancer, and is influenced by patient‐, tumor‐, and treatment‐related factors. We aimed to investigate the impact of such factors in a national cohort of patients with epithelial ovarian cancer (EOC)....

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Veröffentlicht in:Journal of thrombosis and haemostasis 2021-04, Vol.19 (4), p.992-1000
Hauptverfasser: Strøm Kahr, Henriette, Christiansen, Ole B., Juul Riddersholm, Signe, Gade, Inger L., Torp‐Pedersen, Christian, Knudsen, Aage, Thorlacius‐Ussing, Ole
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container_end_page 1000
container_issue 4
container_start_page 992
container_title Journal of thrombosis and haemostasis
container_volume 19
creator Strøm Kahr, Henriette
Christiansen, Ole B.
Juul Riddersholm, Signe
Gade, Inger L.
Torp‐Pedersen, Christian
Knudsen, Aage
Thorlacius‐Ussing, Ole
description Background and aim Venous thromboembolism (VTE) is associated with excess mortality and morbidity in cancer, and is influenced by patient‐, tumor‐, and treatment‐related factors. We aimed to investigate the impact of such factors in a national cohort of patients with epithelial ovarian cancer (EOC). Methods Patients in the Danish Gynecologic Cancer Database (DGCD) with EOC from 2005 to 2014 were followed from time of diagnosis to VTE, or censoring. Surgery, chemotherapy, and vascular epithelial growth factor (VEGF)‐inhibitors were included as time‐varying exposures in Cox proportional hazard regression models. Results A total of 551 VTE events were registered in 4991 EOC patients. Median follow‐up time was 2.9 years. The 2‐year cumulative incidence of VTE was 7.2%. Patients were at highest risk during the first year after EOC diagnosis. Previous VTE was associated with a hazard ratio (HR) of 3.26 (95% confidence interval [CI] 2.42–4.39). Exposure to major pelvic surgery was associated with a HR of 3.21 (95% CI 2.29–4.50). Exposure to chemotherapy or (VEGF)‐inhibitors were associated with HRs of 1.91 (95% CI 1.56–2.33) and 1.05 (95% CI 0.57–1.93), respectively. Hazard ratios for patients with clear cell histopathology was 1.46 (95% CI 0.97–2.20) and 2.42 for International Federation of Gynaecology and Obstetrics stage III‐‐IV (95% CI 1.93–3.03). Conclusions EOC is associated with a high risk of VTE, particularly within the first year after diagnosis. Major pelvic surgery and chemotherapy were strongly associated with VTE. Person‐related risk factors were increasing age and previous VTE. Advanced stage was an independent tumor‐related risk factor. These findings support the indication for thrombosis prophylaxis during chemotherapy.
doi_str_mv 10.1111/jth.15235
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We aimed to investigate the impact of such factors in a national cohort of patients with epithelial ovarian cancer (EOC). Methods Patients in the Danish Gynecologic Cancer Database (DGCD) with EOC from 2005 to 2014 were followed from time of diagnosis to VTE, or censoring. Surgery, chemotherapy, and vascular epithelial growth factor (VEGF)‐inhibitors were included as time‐varying exposures in Cox proportional hazard regression models. Results A total of 551 VTE events were registered in 4991 EOC patients. Median follow‐up time was 2.9 years. The 2‐year cumulative incidence of VTE was 7.2%. Patients were at highest risk during the first year after EOC diagnosis. Previous VTE was associated with a hazard ratio (HR) of 3.26 (95% confidence interval [CI] 2.42–4.39). Exposure to major pelvic surgery was associated with a HR of 3.21 (95% CI 2.29–4.50). Exposure to chemotherapy or (VEGF)‐inhibitors were associated with HRs of 1.91 (95% CI 1.56–2.33) and 1.05 (95% CI 0.57–1.93), respectively. Hazard ratios for patients with clear cell histopathology was 1.46 (95% CI 0.97–2.20) and 2.42 for International Federation of Gynaecology and Obstetrics stage III‐‐IV (95% CI 1.93–3.03). Conclusions EOC is associated with a high risk of VTE, particularly within the first year after diagnosis. Major pelvic surgery and chemotherapy were strongly associated with VTE. Person‐related risk factors were increasing age and previous VTE. Advanced stage was an independent tumor‐related risk factor. These findings support the indication for thrombosis prophylaxis during chemotherapy.</description><identifier>ISSN: 1538-7933</identifier><identifier>ISSN: 1538-7836</identifier><identifier>EISSN: 1538-7836</identifier><identifier>DOI: 10.1111/jth.15235</identifier><identifier>PMID: 33420762</identifier><language>eng</language><publisher>England: Elsevier Limited</publisher><subject>Carcinoma, Ovarian Epithelial - epidemiology ; Chemotherapy ; Cohort analysis ; Cohort Studies ; deep vein thrombosis ; Denmark - epidemiology ; Diagnosis ; epithelial ovarian cancer ; Female ; Fibroblast growth factor 2 ; Humans ; Incidence ; Morbidity ; Obstetrics ; Ovarian cancer ; Ovarian Neoplasms - drug therapy ; Ovarian Neoplasms - epidemiology ; Patients ; Prophylaxis ; Pulmonary Embolism ; Pulmonary embolisms ; Regression analysis ; Risk Factors ; Surgery ; Thromboembolism ; Thrombosis ; Vascular endothelial growth factor ; venous thromboembolism ; Venous Thromboembolism - diagnosis ; Venous Thromboembolism - epidemiology ; venous thromboprophylaxis</subject><ispartof>Journal of thrombosis and haemostasis, 2021-04, Vol.19 (4), p.992-1000</ispartof><rights>2021 International Society on Thrombosis and Haemostasis</rights><rights>2021 International Society on Thrombosis and Haemostasis.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4545-bd0eb58090dbfa399c9bdfa3911b1bebaf60ab9b5c3511cdbb431890adbda7203</citedby><cites>FETCH-LOGICAL-c4545-bd0eb58090dbfa399c9bdfa3911b1bebaf60ab9b5c3511cdbb431890adbda7203</cites><orcidid>0000-0003-0914-7677 ; 0000-0003-0533-5531</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33420762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Strøm Kahr, Henriette</creatorcontrib><creatorcontrib>Christiansen, Ole B.</creatorcontrib><creatorcontrib>Juul Riddersholm, Signe</creatorcontrib><creatorcontrib>Gade, Inger L.</creatorcontrib><creatorcontrib>Torp‐Pedersen, Christian</creatorcontrib><creatorcontrib>Knudsen, Aage</creatorcontrib><creatorcontrib>Thorlacius‐Ussing, Ole</creatorcontrib><title>The timing of venous thromboembolism in ovarian cancer patients: A nationwide Danish cohort study</title><title>Journal of thrombosis and haemostasis</title><addtitle>J Thromb Haemost</addtitle><description>Background and aim Venous thromboembolism (VTE) is associated with excess mortality and morbidity in cancer, and is influenced by patient‐, tumor‐, and treatment‐related factors. We aimed to investigate the impact of such factors in a national cohort of patients with epithelial ovarian cancer (EOC). Methods Patients in the Danish Gynecologic Cancer Database (DGCD) with EOC from 2005 to 2014 were followed from time of diagnosis to VTE, or censoring. Surgery, chemotherapy, and vascular epithelial growth factor (VEGF)‐inhibitors were included as time‐varying exposures in Cox proportional hazard regression models. Results A total of 551 VTE events were registered in 4991 EOC patients. Median follow‐up time was 2.9 years. The 2‐year cumulative incidence of VTE was 7.2%. Patients were at highest risk during the first year after EOC diagnosis. Previous VTE was associated with a hazard ratio (HR) of 3.26 (95% confidence interval [CI] 2.42–4.39). Exposure to major pelvic surgery was associated with a HR of 3.21 (95% CI 2.29–4.50). Exposure to chemotherapy or (VEGF)‐inhibitors were associated with HRs of 1.91 (95% CI 1.56–2.33) and 1.05 (95% CI 0.57–1.93), respectively. Hazard ratios for patients with clear cell histopathology was 1.46 (95% CI 0.97–2.20) and 2.42 for International Federation of Gynaecology and Obstetrics stage III‐‐IV (95% CI 1.93–3.03). Conclusions EOC is associated with a high risk of VTE, particularly within the first year after diagnosis. Major pelvic surgery and chemotherapy were strongly associated with VTE. Person‐related risk factors were increasing age and previous VTE. Advanced stage was an independent tumor‐related risk factor. 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Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strøm Kahr, Henriette</au><au>Christiansen, Ole B.</au><au>Juul Riddersholm, Signe</au><au>Gade, Inger L.</au><au>Torp‐Pedersen, Christian</au><au>Knudsen, Aage</au><au>Thorlacius‐Ussing, Ole</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The timing of venous thromboembolism in ovarian cancer patients: A nationwide Danish cohort study</atitle><jtitle>Journal of thrombosis and haemostasis</jtitle><addtitle>J Thromb Haemost</addtitle><date>2021-04</date><risdate>2021</risdate><volume>19</volume><issue>4</issue><spage>992</spage><epage>1000</epage><pages>992-1000</pages><issn>1538-7933</issn><issn>1538-7836</issn><eissn>1538-7836</eissn><abstract>Background and aim Venous thromboembolism (VTE) is associated with excess mortality and morbidity in cancer, and is influenced by patient‐, tumor‐, and treatment‐related factors. We aimed to investigate the impact of such factors in a national cohort of patients with epithelial ovarian cancer (EOC). Methods Patients in the Danish Gynecologic Cancer Database (DGCD) with EOC from 2005 to 2014 were followed from time of diagnosis to VTE, or censoring. Surgery, chemotherapy, and vascular epithelial growth factor (VEGF)‐inhibitors were included as time‐varying exposures in Cox proportional hazard regression models. Results A total of 551 VTE events were registered in 4991 EOC patients. Median follow‐up time was 2.9 years. The 2‐year cumulative incidence of VTE was 7.2%. Patients were at highest risk during the first year after EOC diagnosis. Previous VTE was associated with a hazard ratio (HR) of 3.26 (95% confidence interval [CI] 2.42–4.39). Exposure to major pelvic surgery was associated with a HR of 3.21 (95% CI 2.29–4.50). Exposure to chemotherapy or (VEGF)‐inhibitors were associated with HRs of 1.91 (95% CI 1.56–2.33) and 1.05 (95% CI 0.57–1.93), respectively. Hazard ratios for patients with clear cell histopathology was 1.46 (95% CI 0.97–2.20) and 2.42 for International Federation of Gynaecology and Obstetrics stage III‐‐IV (95% CI 1.93–3.03). Conclusions EOC is associated with a high risk of VTE, particularly within the first year after diagnosis. Major pelvic surgery and chemotherapy were strongly associated with VTE. Person‐related risk factors were increasing age and previous VTE. Advanced stage was an independent tumor‐related risk factor. These findings support the indication for thrombosis prophylaxis during chemotherapy.</abstract><cop>England</cop><pub>Elsevier Limited</pub><pmid>33420762</pmid><doi>10.1111/jth.15235</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-0914-7677</orcidid><orcidid>https://orcid.org/0000-0003-0533-5531</orcidid><oa>free_for_read</oa></addata></record>
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subjects Carcinoma, Ovarian Epithelial - epidemiology
Chemotherapy
Cohort analysis
Cohort Studies
deep vein thrombosis
Denmark - epidemiology
Diagnosis
epithelial ovarian cancer
Female
Fibroblast growth factor 2
Humans
Incidence
Morbidity
Obstetrics
Ovarian cancer
Ovarian Neoplasms - drug therapy
Ovarian Neoplasms - epidemiology
Patients
Prophylaxis
Pulmonary Embolism
Pulmonary embolisms
Regression analysis
Risk Factors
Surgery
Thromboembolism
Thrombosis
Vascular endothelial growth factor
venous thromboembolism
Venous Thromboembolism - diagnosis
Venous Thromboembolism - epidemiology
venous thromboprophylaxis
title The timing of venous thromboembolism in ovarian cancer patients: A nationwide Danish cohort study
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