Edoxaban for treatment of venous thromboembolism in patients with cancer
Summary Direct oral anticoagulants may be effective and safe for treatment of venous thromboembolism (VTE) in cancer patients, but they have not been compared with low-molecular-weight heparin (LMWH), the current recommended treatment for these patients. The Hokusai VTE-cancer study is a randomised,...
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Veröffentlicht in: | Thrombosis and haemostasis 2015, Vol.113 (6), p.1268-1276 |
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creator | van Es, Nick Di Nisio, Marcello Bleker, Suzanne M. Segers, Annelise Mercuri, Michele F. Schwocho, Lee Kakkar, Ajay Weitz, Jeffrey I. Beyer-Westendorf, Jan Boda, Zoltan Carrier, Marc Chlumsky, Jaromir Décousus, Hervé Garcia, David Gibbs, Harry Kamphuisen, Pieter W. Monreal, Manuel Ockelford, Paul Pabinger, Ingrid Verhamme, Peter Grosso, Michael A. Büller, Harry R. Raskob, Gary E. |
description | Summary
Direct oral anticoagulants may be effective and safe for treatment of venous thromboembolism (VTE) in cancer patients, but they have not been compared with low-molecular-weight heparin (LMWH), the current recommended treatment for these patients. The Hokusai VTE-cancer study is a randomised, open-label, clinical trial to evaluate whether edoxaban, an oral factor Xa inhibitor, is non-inferior to LMWH for treatment of VTE in patients with cancer. We present the rationale and some design features of the study. One such feature is the composite primary outcome of recurrent VTE and major bleeding during a 12-month study period. These two complications occur frequently in cancer patients receiving anticoagulant treatment and have a significant impact. The evaluation beyond six months will fill the current gap in the evidence base for the long-term treatment of these patients. Based on the observation that the risk of recurrent VTE in patients with active cancer is similar to that in those with a history of cancer, the Hokusai VTE-cancer study will enrol patients if whose cancer was diagnosed within the past two years. In addition, patients with incidental VTE are eligible because their risk of recurrent VTE is similar to that in patients with symptomatic disease. The unique design features of the Hokusai VTE-cancer study should lead to enrolment of a broad spectrum of cancer patients with VTE who could benefit from oral anticoagulant treatment. |
doi_str_mv | 10.1160/TH15-06-0452 |
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Direct oral anticoagulants may be effective and safe for treatment of venous thromboembolism (VTE) in cancer patients, but they have not been compared with low-molecular-weight heparin (LMWH), the current recommended treatment for these patients. The Hokusai VTE-cancer study is a randomised, open-label, clinical trial to evaluate whether edoxaban, an oral factor Xa inhibitor, is non-inferior to LMWH for treatment of VTE in patients with cancer. We present the rationale and some design features of the study. One such feature is the composite primary outcome of recurrent VTE and major bleeding during a 12-month study period. These two complications occur frequently in cancer patients receiving anticoagulant treatment and have a significant impact. The evaluation beyond six months will fill the current gap in the evidence base for the long-term treatment of these patients. Based on the observation that the risk of recurrent VTE in patients with active cancer is similar to that in those with a history of cancer, the Hokusai VTE-cancer study will enrol patients if whose cancer was diagnosed within the past two years. In addition, patients with incidental VTE are eligible because their risk of recurrent VTE is similar to that in patients with symptomatic disease. The unique design features of the Hokusai VTE-cancer study should lead to enrolment of a broad spectrum of cancer patients with VTE who could benefit from oral anticoagulant treatment.</description><identifier>ISSN: 0340-6245</identifier><identifier>EISSN: 2567-689X</identifier><identifier>DOI: 10.1160/TH15-06-0452</identifier><language>eng</language><publisher>Schattauer GmbH</publisher><subject>Stroke, Systemic or Venous Thromboembolism</subject><ispartof>Thrombosis and haemostasis, 2015, Vol.113 (6), p.1268-1276</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c792-6c9b4512eac38b9b3fa24b0b745a27657dcd9ead79e850e39b7ab93a31edd9233</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH15-06-0452.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1160/TH15-06-0452$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3005,4010,27900,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>van Es, Nick</creatorcontrib><creatorcontrib>Di Nisio, Marcello</creatorcontrib><creatorcontrib>Bleker, Suzanne M.</creatorcontrib><creatorcontrib>Segers, Annelise</creatorcontrib><creatorcontrib>Mercuri, Michele F.</creatorcontrib><creatorcontrib>Schwocho, Lee</creatorcontrib><creatorcontrib>Kakkar, Ajay</creatorcontrib><creatorcontrib>Weitz, Jeffrey I.</creatorcontrib><creatorcontrib>Beyer-Westendorf, Jan</creatorcontrib><creatorcontrib>Boda, Zoltan</creatorcontrib><creatorcontrib>Carrier, Marc</creatorcontrib><creatorcontrib>Chlumsky, Jaromir</creatorcontrib><creatorcontrib>Décousus, Hervé</creatorcontrib><creatorcontrib>Garcia, David</creatorcontrib><creatorcontrib>Gibbs, Harry</creatorcontrib><creatorcontrib>Kamphuisen, Pieter W.</creatorcontrib><creatorcontrib>Monreal, Manuel</creatorcontrib><creatorcontrib>Ockelford, Paul</creatorcontrib><creatorcontrib>Pabinger, Ingrid</creatorcontrib><creatorcontrib>Verhamme, Peter</creatorcontrib><creatorcontrib>Grosso, Michael A.</creatorcontrib><creatorcontrib>Büller, Harry R.</creatorcontrib><creatorcontrib>Raskob, Gary E.</creatorcontrib><title>Edoxaban for treatment of venous thromboembolism in patients with cancer</title><title>Thrombosis and haemostasis</title><addtitle>Thromb Haemost</addtitle><description>Summary
Direct oral anticoagulants may be effective and safe for treatment of venous thromboembolism (VTE) in cancer patients, but they have not been compared with low-molecular-weight heparin (LMWH), the current recommended treatment for these patients. The Hokusai VTE-cancer study is a randomised, open-label, clinical trial to evaluate whether edoxaban, an oral factor Xa inhibitor, is non-inferior to LMWH for treatment of VTE in patients with cancer. We present the rationale and some design features of the study. One such feature is the composite primary outcome of recurrent VTE and major bleeding during a 12-month study period. These two complications occur frequently in cancer patients receiving anticoagulant treatment and have a significant impact. The evaluation beyond six months will fill the current gap in the evidence base for the long-term treatment of these patients. Based on the observation that the risk of recurrent VTE in patients with active cancer is similar to that in those with a history of cancer, the Hokusai VTE-cancer study will enrol patients if whose cancer was diagnosed within the past two years. In addition, patients with incidental VTE are eligible because their risk of recurrent VTE is similar to that in patients with symptomatic disease. The unique design features of the Hokusai VTE-cancer study should lead to enrolment of a broad spectrum of cancer patients with VTE who could benefit from oral anticoagulant treatment.</description><subject>Stroke, Systemic or Venous Thromboembolism</subject><issn>0340-6245</issn><issn>2567-689X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNotkM1KxDAYRYMoWEd3PkD2Es1_mqUMoyMMuOnCXUjar7TDNJEmoz6-Lbq43M3lXDgI3TP6yJimT82eKUI1oVLxC1RxpQ3Rtf24RBUVkhLNpbpGNzkfKWVaWlWh_a5LPz74iPs04zKDLxPEglOPvyCmc8ZlmNMUEiw5jXnCY8SfvozLKOPvsQy49bGF-RZd9f6U4e6_N6h52TXbPTm8v75tnw-kNZYT3dogFePgW1EHG0TvuQw0GKk8N1qZru0s-M5YqBUFYYPxwQovGHSd5UJs0MMftgwjTOCO6TzH5c8x6lYHbnXgqHarA_ELrSFQAw</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>van Es, Nick</creator><creator>Di Nisio, Marcello</creator><creator>Bleker, Suzanne M.</creator><creator>Segers, Annelise</creator><creator>Mercuri, Michele F.</creator><creator>Schwocho, Lee</creator><creator>Kakkar, Ajay</creator><creator>Weitz, Jeffrey I.</creator><creator>Beyer-Westendorf, Jan</creator><creator>Boda, Zoltan</creator><creator>Carrier, Marc</creator><creator>Chlumsky, Jaromir</creator><creator>Décousus, Hervé</creator><creator>Garcia, David</creator><creator>Gibbs, Harry</creator><creator>Kamphuisen, Pieter W.</creator><creator>Monreal, Manuel</creator><creator>Ockelford, Paul</creator><creator>Pabinger, Ingrid</creator><creator>Verhamme, Peter</creator><creator>Grosso, Michael A.</creator><creator>Büller, Harry R.</creator><creator>Raskob, Gary E.</creator><general>Schattauer GmbH</general><scope/></search><sort><creationdate>2015</creationdate><title>Edoxaban for treatment of venous thromboembolism in patients with cancer</title><author>van Es, Nick ; Di Nisio, Marcello ; Bleker, Suzanne M. ; Segers, Annelise ; Mercuri, Michele F. ; Schwocho, Lee ; Kakkar, Ajay ; Weitz, Jeffrey I. ; Beyer-Westendorf, Jan ; Boda, Zoltan ; Carrier, Marc ; Chlumsky, Jaromir ; Décousus, Hervé ; Garcia, David ; Gibbs, Harry ; Kamphuisen, Pieter W. ; Monreal, Manuel ; Ockelford, Paul ; Pabinger, Ingrid ; Verhamme, Peter ; Grosso, Michael A. ; Büller, Harry R. ; Raskob, Gary E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c792-6c9b4512eac38b9b3fa24b0b745a27657dcd9ead79e850e39b7ab93a31edd9233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Stroke, Systemic or Venous Thromboembolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Es, Nick</creatorcontrib><creatorcontrib>Di Nisio, Marcello</creatorcontrib><creatorcontrib>Bleker, Suzanne M.</creatorcontrib><creatorcontrib>Segers, Annelise</creatorcontrib><creatorcontrib>Mercuri, Michele F.</creatorcontrib><creatorcontrib>Schwocho, Lee</creatorcontrib><creatorcontrib>Kakkar, Ajay</creatorcontrib><creatorcontrib>Weitz, Jeffrey I.</creatorcontrib><creatorcontrib>Beyer-Westendorf, Jan</creatorcontrib><creatorcontrib>Boda, Zoltan</creatorcontrib><creatorcontrib>Carrier, Marc</creatorcontrib><creatorcontrib>Chlumsky, Jaromir</creatorcontrib><creatorcontrib>Décousus, Hervé</creatorcontrib><creatorcontrib>Garcia, David</creatorcontrib><creatorcontrib>Gibbs, Harry</creatorcontrib><creatorcontrib>Kamphuisen, Pieter W.</creatorcontrib><creatorcontrib>Monreal, Manuel</creatorcontrib><creatorcontrib>Ockelford, Paul</creatorcontrib><creatorcontrib>Pabinger, Ingrid</creatorcontrib><creatorcontrib>Verhamme, Peter</creatorcontrib><creatorcontrib>Grosso, Michael A.</creatorcontrib><creatorcontrib>Büller, Harry R.</creatorcontrib><creatorcontrib>Raskob, Gary E.</creatorcontrib><jtitle>Thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Es, Nick</au><au>Di Nisio, Marcello</au><au>Bleker, Suzanne M.</au><au>Segers, Annelise</au><au>Mercuri, Michele F.</au><au>Schwocho, Lee</au><au>Kakkar, Ajay</au><au>Weitz, Jeffrey I.</au><au>Beyer-Westendorf, Jan</au><au>Boda, Zoltan</au><au>Carrier, Marc</au><au>Chlumsky, Jaromir</au><au>Décousus, Hervé</au><au>Garcia, David</au><au>Gibbs, Harry</au><au>Kamphuisen, Pieter W.</au><au>Monreal, Manuel</au><au>Ockelford, Paul</au><au>Pabinger, Ingrid</au><au>Verhamme, Peter</au><au>Grosso, Michael A.</au><au>Büller, Harry R.</au><au>Raskob, Gary E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Edoxaban for treatment of venous thromboembolism in patients with cancer</atitle><jtitle>Thrombosis and haemostasis</jtitle><addtitle>Thromb Haemost</addtitle><date>2015</date><risdate>2015</risdate><volume>113</volume><issue>6</issue><spage>1268</spage><epage>1276</epage><pages>1268-1276</pages><issn>0340-6245</issn><eissn>2567-689X</eissn><abstract>Summary
Direct oral anticoagulants may be effective and safe for treatment of venous thromboembolism (VTE) in cancer patients, but they have not been compared with low-molecular-weight heparin (LMWH), the current recommended treatment for these patients. The Hokusai VTE-cancer study is a randomised, open-label, clinical trial to evaluate whether edoxaban, an oral factor Xa inhibitor, is non-inferior to LMWH for treatment of VTE in patients with cancer. We present the rationale and some design features of the study. One such feature is the composite primary outcome of recurrent VTE and major bleeding during a 12-month study period. These two complications occur frequently in cancer patients receiving anticoagulant treatment and have a significant impact. The evaluation beyond six months will fill the current gap in the evidence base for the long-term treatment of these patients. Based on the observation that the risk of recurrent VTE in patients with active cancer is similar to that in those with a history of cancer, the Hokusai VTE-cancer study will enrol patients if whose cancer was diagnosed within the past two years. In addition, patients with incidental VTE are eligible because their risk of recurrent VTE is similar to that in patients with symptomatic disease. The unique design features of the Hokusai VTE-cancer study should lead to enrolment of a broad spectrum of cancer patients with VTE who could benefit from oral anticoagulant treatment.</abstract><pub>Schattauer GmbH</pub><doi>10.1160/TH15-06-0452</doi><tpages>9</tpages></addata></record> |
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subjects | Stroke, Systemic or Venous Thromboembolism |
title | Edoxaban for treatment of venous thromboembolism in patients with cancer |
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