Extended treatment of cancer-associated thrombosis
Venous thromboembolism (VTE) is a growing concern in patients with cancer. Current guidelines recommend that cancer patients with VTE should receive anticoagulation for at least 3–6 months. However, the question as to whether anticoagulants should be continued after 3 to 6 months of treatment remain...
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Veröffentlicht in: | Thrombosis research 2019-09, Vol.181, p.1-9 |
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creator | Marin-Romero, Samira Jara-Palomares, Luis |
description | Venous thromboembolism (VTE) is a growing concern in patients with cancer. Current guidelines recommend that cancer patients with VTE should receive anticoagulation for at least 3–6 months. However, the question as to whether anticoagulants should be continued after 3 to 6 months of treatment remains open. In presence of an active malignancy, physicians should weigh the benefits and burdens of ongoing anticoagulation taking into account the clinical status, patient expectations, and the risk of bleeding. As the length of time from the index event increases, the available evidence is not conclusive. The most critical unresolved issues include the decision to continue or discontinue anticoagulation and the selection of the most appropriate anticoagulant agent. On this background, our article provides an overview of the available studies focusing on extended (i.e., >6 months) anticoagulation treatment in cancer-associated thrombosis, with the ultimate goal of refining real-world clinical decision-making in this patient population.
•The current evidence about extended treatment in patient with CAT is inconclusive.•Prospective and retrospective studies, trials and reviews were evaluated.•Anticoagulant therapy must be maintained while there is an active cancer.•Consider DOAC in CAT with low risk of bleeding and no drug-drug interactions•In CAT, full assessment will allow us to choose the best anticoagulant treatment. |
doi_str_mv | 10.1016/j.thromres.2019.07.003 |
format | Article |
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•The current evidence about extended treatment in patient with CAT is inconclusive.•Prospective and retrospective studies, trials and reviews were evaluated.•Anticoagulant therapy must be maintained while there is an active cancer.•Consider DOAC in CAT with low risk of bleeding and no drug-drug interactions•In CAT, full assessment will allow us to choose the best anticoagulant treatment.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2019.07.003</identifier><identifier>PMID: 31302473</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Aged ; Anticoagulants - pharmacology ; Anticoagulants - therapeutic use ; Anticoagulation ; Cancer ; Extended treatment ; Female ; Humans ; Male ; Middle Aged ; Neoplasms - complications ; Neoplasms - drug therapy ; Neoplasms - pathology ; Risk Factors ; Thrombosis - drug therapy ; Venous thromboembolism ; Venous Thromboembolism - drug therapy</subject><ispartof>Thrombosis research, 2019-09, Vol.181, p.1-9</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-458a77978876ff7641492b9047cf1fc91048890ec47a8cee5b40feca9397681a3</citedby><cites>FETCH-LOGICAL-c368t-458a77978876ff7641492b9047cf1fc91048890ec47a8cee5b40feca9397681a3</cites><orcidid>0000-0002-4125-3376</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0049384819302865$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31302473$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marin-Romero, Samira</creatorcontrib><creatorcontrib>Jara-Palomares, Luis</creatorcontrib><title>Extended treatment of cancer-associated thrombosis</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>Venous thromboembolism (VTE) is a growing concern in patients with cancer. Current guidelines recommend that cancer patients with VTE should receive anticoagulation for at least 3–6 months. However, the question as to whether anticoagulants should be continued after 3 to 6 months of treatment remains open. In presence of an active malignancy, physicians should weigh the benefits and burdens of ongoing anticoagulation taking into account the clinical status, patient expectations, and the risk of bleeding. As the length of time from the index event increases, the available evidence is not conclusive. The most critical unresolved issues include the decision to continue or discontinue anticoagulation and the selection of the most appropriate anticoagulant agent. On this background, our article provides an overview of the available studies focusing on extended (i.e., >6 months) anticoagulation treatment in cancer-associated thrombosis, with the ultimate goal of refining real-world clinical decision-making in this patient population.
•The current evidence about extended treatment in patient with CAT is inconclusive.•Prospective and retrospective studies, trials and reviews were evaluated.•Anticoagulant therapy must be maintained while there is an active cancer.•Consider DOAC in CAT with low risk of bleeding and no drug-drug interactions•In CAT, full assessment will allow us to choose the best anticoagulant treatment.</description><subject>Aged</subject><subject>Anticoagulants - pharmacology</subject><subject>Anticoagulants - therapeutic use</subject><subject>Anticoagulation</subject><subject>Cancer</subject><subject>Extended treatment</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasms - complications</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - pathology</subject><subject>Risk Factors</subject><subject>Thrombosis - drug therapy</subject><subject>Venous thromboembolism</subject><subject>Venous Thromboembolism - drug therapy</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EoqXwF6qOLAnn2IntDVSVD6kSC8yW45yFqyYptovg35OoLSvTDfe89-oeQuYUcgq0utvk6SP0bcCYF0BVDiIHYGdkSqVQWcFFcU6mAFxlTHI5IVcxbgCooKq8JBNGGQwMm5Ji9Z2wa7BZpIAmtdilRe8W1nQWQ2Zi7K03aVyPdXUffbwmF85sI94c54y8P67els_Z-vXpZfmwziyrZMp4KY0QSkgpKudExSlXRa2AC-uos4oCl1IBWi6MtIhlzcGhNYopUUlq2IzcHu7uQv-5x5h066PF7dZ02O-jLopS0rICBgNaHVAb-hgDOr0LvjXhR1PQoy-90SdfevSlQejB1xCcHzv2dYvNX-wkaADuDwAOn355DDpaj4Ocxge0STe9_6_jFzOifs4</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Marin-Romero, Samira</creator><creator>Jara-Palomares, Luis</creator><general>Elsevier Ltd</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><orcidid>https://orcid.org/0000-0002-4125-3376</orcidid></search><sort><creationdate>201909</creationdate><title>Extended treatment of cancer-associated thrombosis</title><author>Marin-Romero, Samira ; Jara-Palomares, Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-458a77978876ff7641492b9047cf1fc91048890ec47a8cee5b40feca9397681a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aged</topic><topic>Anticoagulants - pharmacology</topic><topic>Anticoagulants - therapeutic use</topic><topic>Anticoagulation</topic><topic>Cancer</topic><topic>Extended treatment</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasms - complications</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - pathology</topic><topic>Risk Factors</topic><topic>Thrombosis - drug therapy</topic><topic>Venous thromboembolism</topic><topic>Venous Thromboembolism - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marin-Romero, Samira</creatorcontrib><creatorcontrib>Jara-Palomares, Luis</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>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marin-Romero, Samira</au><au>Jara-Palomares, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extended treatment of cancer-associated thrombosis</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2019-09</date><risdate>2019</risdate><volume>181</volume><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><abstract>Venous thromboembolism (VTE) is a growing concern in patients with cancer. Current guidelines recommend that cancer patients with VTE should receive anticoagulation for at least 3–6 months. However, the question as to whether anticoagulants should be continued after 3 to 6 months of treatment remains open. In presence of an active malignancy, physicians should weigh the benefits and burdens of ongoing anticoagulation taking into account the clinical status, patient expectations, and the risk of bleeding. As the length of time from the index event increases, the available evidence is not conclusive. The most critical unresolved issues include the decision to continue or discontinue anticoagulation and the selection of the most appropriate anticoagulant agent. On this background, our article provides an overview of the available studies focusing on extended (i.e., >6 months) anticoagulation treatment in cancer-associated thrombosis, with the ultimate goal of refining real-world clinical decision-making in this patient population.
•The current evidence about extended treatment in patient with CAT is inconclusive.•Prospective and retrospective studies, trials and reviews were evaluated.•Anticoagulant therapy must be maintained while there is an active cancer.•Consider DOAC in CAT with low risk of bleeding and no drug-drug interactions•In CAT, full assessment will allow us to choose the best anticoagulant treatment.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>31302473</pmid><doi>10.1016/j.thromres.2019.07.003</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4125-3376</orcidid></addata></record> |
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subjects | Aged Anticoagulants - pharmacology Anticoagulants - therapeutic use Anticoagulation Cancer Extended treatment Female Humans Male Middle Aged Neoplasms - complications Neoplasms - drug therapy Neoplasms - pathology Risk Factors Thrombosis - drug therapy Venous thromboembolism Venous Thromboembolism - drug therapy |
title | Extended treatment of cancer-associated thrombosis |
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