Current practice patterns and patient persistence with anticoagulant treatments for cancer‐associated thrombosis
Recommended therapeutic options for the management of venous thromboembolism (VTE) in patients with cancer are burdensome, and compliance with guidelines is unknown. To describe current treatment patterns and to evaluate patient persistence on various anticoagulants. Medical and pharmacy claims from...
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creator | Khorana, Alok A. McCrae, Keith R. Milentijevic, Dejan Fortier, Jonathan Nelson, Winnie W. Laliberté, François Crivera, Concetta Lefebvre, Patrick Yannicelli, Daniel Schein, Jeff |
description | Recommended therapeutic options for the management of venous thromboembolism (VTE) in patients with cancer are burdensome, and compliance with guidelines is unknown.
To describe current treatment patterns and to evaluate patient persistence on various anticoagulants.
Medical and pharmacy claims from the Humana Database were analyzed (01/2007‐12/2014). Newly diagnosed cancer patients treated with anticoagulants were categorized into one of the following cohorts: low–molecular‐weight heparin (LMWH), warfarin, and rivaroxaban. Discontinuation, switching, and persistence with the index therapy were analyzed.
A total of 2941 newly diagnosed patients with cancer who developed VTE and received anticoagulation in outpatient settings were identified. Of these, 97% initiated anticoagulation with LMWH (n=735; 25%), warfarin (n=1403; 47.7%), or rivaroxaban (n=709; 24.1%). Median treatment durations for the LMWH, warfarin, and rivaroxaban cohorts were 3.3, 7.9, and 7.9 months, respectively; Kaplan‐Meier rates of persistence to the initial therapy were 37%, 61%, and 61% at 6 months. Warfarin and rivaroxaban users were significantly more likely to remain on initial therapy compared to LMWH (adjusted hazard ratios [HRs; 95% CI]: warfarin, 0.33 [0.28‐0.38]; rivaroxaban, 0.38 [0.32‐0.46]). The proportion of patients that switched from their initial treatment to another anticoagulation treatment was 22.9%, 7.9%, and 4.7% in the LMWH, warfarin, and rivaroxaban cohorts, respectively.
This real‐world analysis showed that, despite guideline recommendations, warfarin and rivaroxaban are at least as equally utilized as LMWH for the treatment of cancer‐associated thrombosis. LMWH was associated with significantly lower persistence, shorter duration of treatment, and more switching than warfarin and rivaroxaban. |
doi_str_mv | 10.1002/rth2.12002 |
format | Article |
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To describe current treatment patterns and to evaluate patient persistence on various anticoagulants.
Medical and pharmacy claims from the Humana Database were analyzed (01/2007‐12/2014). Newly diagnosed cancer patients treated with anticoagulants were categorized into one of the following cohorts: low–molecular‐weight heparin (LMWH), warfarin, and rivaroxaban. Discontinuation, switching, and persistence with the index therapy were analyzed.
A total of 2941 newly diagnosed patients with cancer who developed VTE and received anticoagulation in outpatient settings were identified. Of these, 97% initiated anticoagulation with LMWH (n=735; 25%), warfarin (n=1403; 47.7%), or rivaroxaban (n=709; 24.1%). Median treatment durations for the LMWH, warfarin, and rivaroxaban cohorts were 3.3, 7.9, and 7.9 months, respectively; Kaplan‐Meier rates of persistence to the initial therapy were 37%, 61%, and 61% at 6 months. Warfarin and rivaroxaban users were significantly more likely to remain on initial therapy compared to LMWH (adjusted hazard ratios [HRs; 95% CI]: warfarin, 0.33 [0.28‐0.38]; rivaroxaban, 0.38 [0.32‐0.46]). The proportion of patients that switched from their initial treatment to another anticoagulation treatment was 22.9%, 7.9%, and 4.7% in the LMWH, warfarin, and rivaroxaban cohorts, respectively.
This real‐world analysis showed that, despite guideline recommendations, warfarin and rivaroxaban are at least as equally utilized as LMWH for the treatment of cancer‐associated thrombosis. LMWH was associated with significantly lower persistence, shorter duration of treatment, and more switching than warfarin and rivaroxaban.</description><identifier>ISSN: 2475-0379</identifier><identifier>EISSN: 2475-0379</identifier><identifier>DOI: 10.1002/rth2.12002</identifier><identifier>PMID: 30046670</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>anticoagulant ; Anticoagulants ; cancer ; Cancer therapies ; Chemotherapy ; Clinical trials ; Data analysis ; deep vein thrombosis ; Medical diagnosis ; Original ; Patients ; Pharmacy ; pulmonary embolism ; Pulmonary embolisms ; Thrombosis ; venous thromboembolism</subject><ispartof>Research and practice in thrombosis and haemostasis, 2017-07, Vol.1 (1), p.14-22</ispartof><rights>2017 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>2017 The Authors. published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5212-f726148ed2cef069285d350c92d5d01f8355adbd175f5864754164a95f303af63</citedby><cites>FETCH-LOGICAL-c5212-f726148ed2cef069285d350c92d5d01f8355adbd175f5864754164a95f303af63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058198/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058198/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30046670$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khorana, Alok A.</creatorcontrib><creatorcontrib>McCrae, Keith R.</creatorcontrib><creatorcontrib>Milentijevic, Dejan</creatorcontrib><creatorcontrib>Fortier, Jonathan</creatorcontrib><creatorcontrib>Nelson, Winnie W.</creatorcontrib><creatorcontrib>Laliberté, François</creatorcontrib><creatorcontrib>Crivera, Concetta</creatorcontrib><creatorcontrib>Lefebvre, Patrick</creatorcontrib><creatorcontrib>Yannicelli, Daniel</creatorcontrib><creatorcontrib>Schein, Jeff</creatorcontrib><title>Current practice patterns and patient persistence with anticoagulant treatments for cancer‐associated thrombosis</title><title>Research and practice in thrombosis and haemostasis</title><addtitle>Res Pract Thromb Haemost</addtitle><description>Recommended therapeutic options for the management of venous thromboembolism (VTE) in patients with cancer are burdensome, and compliance with guidelines is unknown.
To describe current treatment patterns and to evaluate patient persistence on various anticoagulants.
Medical and pharmacy claims from the Humana Database were analyzed (01/2007‐12/2014). Newly diagnosed cancer patients treated with anticoagulants were categorized into one of the following cohorts: low–molecular‐weight heparin (LMWH), warfarin, and rivaroxaban. Discontinuation, switching, and persistence with the index therapy were analyzed.
A total of 2941 newly diagnosed patients with cancer who developed VTE and received anticoagulation in outpatient settings were identified. Of these, 97% initiated anticoagulation with LMWH (n=735; 25%), warfarin (n=1403; 47.7%), or rivaroxaban (n=709; 24.1%). Median treatment durations for the LMWH, warfarin, and rivaroxaban cohorts were 3.3, 7.9, and 7.9 months, respectively; Kaplan‐Meier rates of persistence to the initial therapy were 37%, 61%, and 61% at 6 months. Warfarin and rivaroxaban users were significantly more likely to remain on initial therapy compared to LMWH (adjusted hazard ratios [HRs; 95% CI]: warfarin, 0.33 [0.28‐0.38]; rivaroxaban, 0.38 [0.32‐0.46]). The proportion of patients that switched from their initial treatment to another anticoagulation treatment was 22.9%, 7.9%, and 4.7% in the LMWH, warfarin, and rivaroxaban cohorts, respectively.
This real‐world analysis showed that, despite guideline recommendations, warfarin and rivaroxaban are at least as equally utilized as LMWH for the treatment of cancer‐associated thrombosis. LMWH was associated with significantly lower persistence, shorter duration of treatment, and more switching than warfarin and rivaroxaban.</description><subject>anticoagulant</subject><subject>Anticoagulants</subject><subject>cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Data analysis</subject><subject>deep vein thrombosis</subject><subject>Medical diagnosis</subject><subject>Original</subject><subject>Patients</subject><subject>Pharmacy</subject><subject>pulmonary embolism</subject><subject>Pulmonary embolisms</subject><subject>Thrombosis</subject><subject>venous thromboembolism</subject><issn>2475-0379</issn><issn>2475-0379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kdFqFTEQhhdRbKm98QFkwRsRTp1kN9ndG0EO1goFQep1yElme1J2N8dJtqV3fQSf0SfpnJ62VBEhkBnmy88_-YvitYAjASA_UF7LIyG5fFbsy7pRC6ia7vmTeq84TOkCmADJR70s9iqAWusG9gtazkQ45XJD1uXgsNzYnJGmVNrJb5twN0VKIWWcGLgKec1DhqM9nweuykxo88hgKvtIpbPM0e-bXzal6ILN6Mu8pjiuIqu8Kl70dkh4eH8fFD-OP58tTxan3758XX46XTglhVz0jdSibtFLhz3oTrbKVwpcJ73yIPq2Usr6lReN6lWredta6Np2qq-gsr2uDoqPO93NvBrRO7ZHdjAbCqOlaxNtMH9OprA25_HSaFCt6FoWeHcvQPHnjCmbMSSHA6-McU5GQqPbroVGMfr2L_QizjTxekbKDppGga6Zer-jHMWUCPtHMwLMNk2zTdPcpcnwm6f2H9GH7BgQO-AqDHj9Hynz_exEPojWuzfIH38ZkExyYZuqD4QuGx_Dv7zcAu31vsk</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Khorana, Alok A.</creator><creator>McCrae, Keith R.</creator><creator>Milentijevic, Dejan</creator><creator>Fortier, Jonathan</creator><creator>Nelson, Winnie W.</creator><creator>Laliberté, François</creator><creator>Crivera, Concetta</creator><creator>Lefebvre, Patrick</creator><creator>Yannicelli, Daniel</creator><creator>Schein, Jeff</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><general>John Wiley and Sons Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201707</creationdate><title>Current practice patterns and patient persistence with anticoagulant treatments for cancer‐associated thrombosis</title><author>Khorana, Alok A. ; McCrae, Keith R. ; Milentijevic, Dejan ; Fortier, Jonathan ; Nelson, Winnie W. ; Laliberté, François ; Crivera, Concetta ; Lefebvre, Patrick ; Yannicelli, Daniel ; Schein, Jeff</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5212-f726148ed2cef069285d350c92d5d01f8355adbd175f5864754164a95f303af63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>anticoagulant</topic><topic>Anticoagulants</topic><topic>cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Data analysis</topic><topic>deep vein thrombosis</topic><topic>Medical diagnosis</topic><topic>Original</topic><topic>Patients</topic><topic>Pharmacy</topic><topic>pulmonary embolism</topic><topic>Pulmonary embolisms</topic><topic>Thrombosis</topic><topic>venous thromboembolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khorana, Alok A.</creatorcontrib><creatorcontrib>McCrae, Keith R.</creatorcontrib><creatorcontrib>Milentijevic, Dejan</creatorcontrib><creatorcontrib>Fortier, Jonathan</creatorcontrib><creatorcontrib>Nelson, Winnie W.</creatorcontrib><creatorcontrib>Laliberté, François</creatorcontrib><creatorcontrib>Crivera, Concetta</creatorcontrib><creatorcontrib>Lefebvre, Patrick</creatorcontrib><creatorcontrib>Yannicelli, Daniel</creatorcontrib><creatorcontrib>Schein, Jeff</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Research and practice in thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khorana, Alok A.</au><au>McCrae, Keith R.</au><au>Milentijevic, Dejan</au><au>Fortier, Jonathan</au><au>Nelson, Winnie W.</au><au>Laliberté, François</au><au>Crivera, Concetta</au><au>Lefebvre, Patrick</au><au>Yannicelli, Daniel</au><au>Schein, Jeff</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current practice patterns and patient persistence with anticoagulant treatments for cancer‐associated thrombosis</atitle><jtitle>Research and practice in thrombosis and haemostasis</jtitle><addtitle>Res Pract Thromb Haemost</addtitle><date>2017-07</date><risdate>2017</risdate><volume>1</volume><issue>1</issue><spage>14</spage><epage>22</epage><pages>14-22</pages><issn>2475-0379</issn><eissn>2475-0379</eissn><abstract>Recommended therapeutic options for the management of venous thromboembolism (VTE) in patients with cancer are burdensome, and compliance with guidelines is unknown.
To describe current treatment patterns and to evaluate patient persistence on various anticoagulants.
Medical and pharmacy claims from the Humana Database were analyzed (01/2007‐12/2014). Newly diagnosed cancer patients treated with anticoagulants were categorized into one of the following cohorts: low–molecular‐weight heparin (LMWH), warfarin, and rivaroxaban. Discontinuation, switching, and persistence with the index therapy were analyzed.
A total of 2941 newly diagnosed patients with cancer who developed VTE and received anticoagulation in outpatient settings were identified. Of these, 97% initiated anticoagulation with LMWH (n=735; 25%), warfarin (n=1403; 47.7%), or rivaroxaban (n=709; 24.1%). Median treatment durations for the LMWH, warfarin, and rivaroxaban cohorts were 3.3, 7.9, and 7.9 months, respectively; Kaplan‐Meier rates of persistence to the initial therapy were 37%, 61%, and 61% at 6 months. Warfarin and rivaroxaban users were significantly more likely to remain on initial therapy compared to LMWH (adjusted hazard ratios [HRs; 95% CI]: warfarin, 0.33 [0.28‐0.38]; rivaroxaban, 0.38 [0.32‐0.46]). The proportion of patients that switched from their initial treatment to another anticoagulation treatment was 22.9%, 7.9%, and 4.7% in the LMWH, warfarin, and rivaroxaban cohorts, respectively.
This real‐world analysis showed that, despite guideline recommendations, warfarin and rivaroxaban are at least as equally utilized as LMWH for the treatment of cancer‐associated thrombosis. LMWH was associated with significantly lower persistence, shorter duration of treatment, and more switching than warfarin and rivaroxaban.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30046670</pmid><doi>10.1002/rth2.12002</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | anticoagulant Anticoagulants cancer Cancer therapies Chemotherapy Clinical trials Data analysis deep vein thrombosis Medical diagnosis Original Patients Pharmacy pulmonary embolism Pulmonary embolisms Thrombosis venous thromboembolism |
title | Current practice patterns and patient persistence with anticoagulant treatments for cancer‐associated thrombosis |
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