Factor Xa Inhibition for the Treatment of Venous Thromboembolism Associated With Cancer: A Meta-Analysis of the Randomised Controlled Trials

Venous thromboembolism (VTE) is a common cause of morbidity and mortality in cancer patients. Until recently, guidelines recommended the use of low-molecular weight heparin (LMWH) as standard of care for VTE in patients with cancer. Despite the proven efficacy of direct oral anticoagulants (DOACs) f...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Heart, lung & circulation lung & circulation, 2022-05, Vol.31 (5), p.716-725
Hauptverfasser: Murphy, Alexandra C., Koshy, Anoop N., Farouque, Omar, Yeo, Belinda, Raman, Jaishankar, Kearney, Leighton, Yudi, Matias B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 725
container_issue 5
container_start_page 716
container_title Heart, lung & circulation
container_volume 31
creator Murphy, Alexandra C.
Koshy, Anoop N.
Farouque, Omar
Yeo, Belinda
Raman, Jaishankar
Kearney, Leighton
Yudi, Matias B.
description Venous thromboembolism (VTE) is a common cause of morbidity and mortality in cancer patients. Until recently, guidelines recommended the use of low-molecular weight heparin (LMWH) as standard of care for VTE in patients with cancer. Despite the proven efficacy of direct oral anticoagulants (DOACs) for treatment of VTE, there is equipoise supporting their use in cancer patients. A systematic review of PubMed, Medline and EMBASE identified four randomised controlled trials (RCTs) in patients with cancer and VTE comparing a factor Xa inhibitor (FXaI) to LMWH. A meta-analysis was performed with a primary outcome of VTE recurrence and key secondary outcomes of major bleeding, clinically relevant non-major bleeding (CRNMB) and gastrointestinal (GI) bleeding. Four RCTs with 2,907 patients were included. 1,451 patients were randomised to FXaI and 1,456 to LMWH. VTE recurrence was lower in the FXaI group (RR 0.62, 95%CI 0.44–0.87; p=0.01; I2=24.90), with an absolute risk difference of -4% equating to a number needed to treat of 25 for prevention of recurrent VTE with FXaI. No significant difference in major bleeding was noted between groups (RR 1.33, 95%CI 0.84–2.11; p=0.23). Rates of GI bleeding (RR 1.87, 95%CI 1.06–3.29; p=0.03) and CRNMB (RR 1.57, 95%CI 1.11–2.23; p=0.01) were greater with FXaIs. In patients with cancer and VTE, the rate of VTE recurrence was significantly lower with FXaI than with LMWH without an increased risk of major bleeding. Our data supports the use of FXaIs as the standard of care for the treatment of VTE in this population.
doi_str_mv 10.1016/j.hlc.2021.10.024
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2609458685</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1443950621013494</els_id><sourcerecordid>2609458685</sourcerecordid><originalsourceid>FETCH-LOGICAL-c353t-c923861c4c0bd2dd244c4ce1df0a70f592cd5b6c4b71f3b508e6ad80997eae733</originalsourceid><addsrcrecordid>eNp9UclqHDEQFSbBW_IBvhgdc-mxtl6UnIYhXsAhECbLTailalpDt-RIGoP_IR9tdcbxMYeiXhWvHlX1ELqgZEUJba52q3EyK0YYLfWKMHGETqkQomKdZG_-Yl7JmjQn6CylHSG0FVweoxMuOtkQyk_Rn2ttcoj4l8Z3fnS9yy54PJROHgFvI-g8g884DPgH-LBPeDvGMPcBSkwuzXidUjBOZ7D4p8sj3mhvIH7Ea_wFsq7WXk9PyaVFYZH8pr0Ns0uFvgk-xzBNBW6j01N6h94OJcH7l3yOvl9_3m5uq_uvN3eb9X1leM1zZSTjXUONMKS3zFomRMFA7UB0S4ZaMmPrvjGib-nA-5p00GjbESlb0NByfo4-HHQfYvi9h5RVWcjANGkP5UTFGiJF3TVdXaj0QDUxpBRhUA_RzTo-KUrUYoLaqWKCWkxYWsWEMnP5Ir_vZ7CvE_--XgifDgQoRz46iCoZB-Vt1kUwWdng_iP_DHbbmT4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2609458685</pqid></control><display><type>article</type><title>Factor Xa Inhibition for the Treatment of Venous Thromboembolism Associated With Cancer: A Meta-Analysis of the Randomised Controlled Trials</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Murphy, Alexandra C. ; Koshy, Anoop N. ; Farouque, Omar ; Yeo, Belinda ; Raman, Jaishankar ; Kearney, Leighton ; Yudi, Matias B.</creator><creatorcontrib>Murphy, Alexandra C. ; Koshy, Anoop N. ; Farouque, Omar ; Yeo, Belinda ; Raman, Jaishankar ; Kearney, Leighton ; Yudi, Matias B.</creatorcontrib><description>Venous thromboembolism (VTE) is a common cause of morbidity and mortality in cancer patients. Until recently, guidelines recommended the use of low-molecular weight heparin (LMWH) as standard of care for VTE in patients with cancer. Despite the proven efficacy of direct oral anticoagulants (DOACs) for treatment of VTE, there is equipoise supporting their use in cancer patients. A systematic review of PubMed, Medline and EMBASE identified four randomised controlled trials (RCTs) in patients with cancer and VTE comparing a factor Xa inhibitor (FXaI) to LMWH. A meta-analysis was performed with a primary outcome of VTE recurrence and key secondary outcomes of major bleeding, clinically relevant non-major bleeding (CRNMB) and gastrointestinal (GI) bleeding. Four RCTs with 2,907 patients were included. 1,451 patients were randomised to FXaI and 1,456 to LMWH. VTE recurrence was lower in the FXaI group (RR 0.62, 95%CI 0.44–0.87; p=0.01; I2=24.90), with an absolute risk difference of -4% equating to a number needed to treat of 25 for prevention of recurrent VTE with FXaI. No significant difference in major bleeding was noted between groups (RR 1.33, 95%CI 0.84–2.11; p=0.23). Rates of GI bleeding (RR 1.87, 95%CI 1.06–3.29; p=0.03) and CRNMB (RR 1.57, 95%CI 1.11–2.23; p=0.01) were greater with FXaIs. In patients with cancer and VTE, the rate of VTE recurrence was significantly lower with FXaI than with LMWH without an increased risk of major bleeding. Our data supports the use of FXaIs as the standard of care for the treatment of VTE in this population.</description><identifier>ISSN: 1443-9506</identifier><identifier>EISSN: 1444-2892</identifier><identifier>DOI: 10.1016/j.hlc.2021.10.024</identifier><identifier>PMID: 34896013</identifier><language>eng</language><publisher>Australia: Elsevier B.V</publisher><subject>Anticoagulants - therapeutic use ; Anticoagulation ; Cancer ; Cardio-oncology ; Direct oral anticoagulation ; Factor Xa ; Factor Xa inhibitor ; Factor Xa Inhibitors - therapeutic use ; Fibrinolytic Agents ; Hemorrhage - chemically induced ; Heparin, Low-Molecular-Weight - therapeutic use ; Humans ; Low molecular weight heparin ; Neoplasms - complications ; Randomized Controlled Trials as Topic ; Venous thromboembolism ; Venous Thromboembolism - drug therapy ; Venous Thromboembolism - etiology</subject><ispartof>Heart, lung &amp; circulation, 2022-05, Vol.31 (5), p.716-725</ispartof><rights>2021 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ)</rights><rights>Copyright © 2021 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-c923861c4c0bd2dd244c4ce1df0a70f592cd5b6c4b71f3b508e6ad80997eae733</citedby><cites>FETCH-LOGICAL-c353t-c923861c4c0bd2dd244c4ce1df0a70f592cd5b6c4b71f3b508e6ad80997eae733</cites><orcidid>0000-0003-2821-1451</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.hlc.2021.10.024$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34896013$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murphy, Alexandra C.</creatorcontrib><creatorcontrib>Koshy, Anoop N.</creatorcontrib><creatorcontrib>Farouque, Omar</creatorcontrib><creatorcontrib>Yeo, Belinda</creatorcontrib><creatorcontrib>Raman, Jaishankar</creatorcontrib><creatorcontrib>Kearney, Leighton</creatorcontrib><creatorcontrib>Yudi, Matias B.</creatorcontrib><title>Factor Xa Inhibition for the Treatment of Venous Thromboembolism Associated With Cancer: A Meta-Analysis of the Randomised Controlled Trials</title><title>Heart, lung &amp; circulation</title><addtitle>Heart Lung Circ</addtitle><description>Venous thromboembolism (VTE) is a common cause of morbidity and mortality in cancer patients. Until recently, guidelines recommended the use of low-molecular weight heparin (LMWH) as standard of care for VTE in patients with cancer. Despite the proven efficacy of direct oral anticoagulants (DOACs) for treatment of VTE, there is equipoise supporting their use in cancer patients. A systematic review of PubMed, Medline and EMBASE identified four randomised controlled trials (RCTs) in patients with cancer and VTE comparing a factor Xa inhibitor (FXaI) to LMWH. A meta-analysis was performed with a primary outcome of VTE recurrence and key secondary outcomes of major bleeding, clinically relevant non-major bleeding (CRNMB) and gastrointestinal (GI) bleeding. Four RCTs with 2,907 patients were included. 1,451 patients were randomised to FXaI and 1,456 to LMWH. VTE recurrence was lower in the FXaI group (RR 0.62, 95%CI 0.44–0.87; p=0.01; I2=24.90), with an absolute risk difference of -4% equating to a number needed to treat of 25 for prevention of recurrent VTE with FXaI. No significant difference in major bleeding was noted between groups (RR 1.33, 95%CI 0.84–2.11; p=0.23). Rates of GI bleeding (RR 1.87, 95%CI 1.06–3.29; p=0.03) and CRNMB (RR 1.57, 95%CI 1.11–2.23; p=0.01) were greater with FXaIs. In patients with cancer and VTE, the rate of VTE recurrence was significantly lower with FXaI than with LMWH without an increased risk of major bleeding. Our data supports the use of FXaIs as the standard of care for the treatment of VTE in this population.</description><subject>Anticoagulants - therapeutic use</subject><subject>Anticoagulation</subject><subject>Cancer</subject><subject>Cardio-oncology</subject><subject>Direct oral anticoagulation</subject><subject>Factor Xa</subject><subject>Factor Xa inhibitor</subject><subject>Factor Xa Inhibitors - therapeutic use</subject><subject>Fibrinolytic Agents</subject><subject>Hemorrhage - chemically induced</subject><subject>Heparin, Low-Molecular-Weight - therapeutic use</subject><subject>Humans</subject><subject>Low molecular weight heparin</subject><subject>Neoplasms - complications</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Venous thromboembolism</subject><subject>Venous Thromboembolism - drug therapy</subject><subject>Venous Thromboembolism - etiology</subject><issn>1443-9506</issn><issn>1444-2892</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UclqHDEQFSbBW_IBvhgdc-mxtl6UnIYhXsAhECbLTailalpDt-RIGoP_IR9tdcbxMYeiXhWvHlX1ELqgZEUJba52q3EyK0YYLfWKMHGETqkQomKdZG_-Yl7JmjQn6CylHSG0FVweoxMuOtkQyk_Rn2ttcoj4l8Z3fnS9yy54PJROHgFvI-g8g884DPgH-LBPeDvGMPcBSkwuzXidUjBOZ7D4p8sj3mhvIH7Ea_wFsq7WXk9PyaVFYZH8pr0Ns0uFvgk-xzBNBW6j01N6h94OJcH7l3yOvl9_3m5uq_uvN3eb9X1leM1zZSTjXUONMKS3zFomRMFA7UB0S4ZaMmPrvjGib-nA-5p00GjbESlb0NByfo4-HHQfYvi9h5RVWcjANGkP5UTFGiJF3TVdXaj0QDUxpBRhUA_RzTo-KUrUYoLaqWKCWkxYWsWEMnP5Ir_vZ7CvE_--XgifDgQoRz46iCoZB-Vt1kUwWdng_iP_DHbbmT4</recordid><startdate>202205</startdate><enddate>202205</enddate><creator>Murphy, Alexandra C.</creator><creator>Koshy, Anoop N.</creator><creator>Farouque, Omar</creator><creator>Yeo, Belinda</creator><creator>Raman, Jaishankar</creator><creator>Kearney, Leighton</creator><creator>Yudi, Matias B.</creator><general>Elsevier B.V</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/0000-0003-2821-1451</orcidid></search><sort><creationdate>202205</creationdate><title>Factor Xa Inhibition for the Treatment of Venous Thromboembolism Associated With Cancer: A Meta-Analysis of the Randomised Controlled Trials</title><author>Murphy, Alexandra C. ; Koshy, Anoop N. ; Farouque, Omar ; Yeo, Belinda ; Raman, Jaishankar ; Kearney, Leighton ; Yudi, Matias B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-c923861c4c0bd2dd244c4ce1df0a70f592cd5b6c4b71f3b508e6ad80997eae733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Anticoagulants - therapeutic use</topic><topic>Anticoagulation</topic><topic>Cancer</topic><topic>Cardio-oncology</topic><topic>Direct oral anticoagulation</topic><topic>Factor Xa</topic><topic>Factor Xa inhibitor</topic><topic>Factor Xa Inhibitors - therapeutic use</topic><topic>Fibrinolytic Agents</topic><topic>Hemorrhage - chemically induced</topic><topic>Heparin, Low-Molecular-Weight - therapeutic use</topic><topic>Humans</topic><topic>Low molecular weight heparin</topic><topic>Neoplasms - complications</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Venous thromboembolism</topic><topic>Venous Thromboembolism - drug therapy</topic><topic>Venous Thromboembolism - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murphy, Alexandra C.</creatorcontrib><creatorcontrib>Koshy, Anoop N.</creatorcontrib><creatorcontrib>Farouque, Omar</creatorcontrib><creatorcontrib>Yeo, Belinda</creatorcontrib><creatorcontrib>Raman, Jaishankar</creatorcontrib><creatorcontrib>Kearney, Leighton</creatorcontrib><creatorcontrib>Yudi, Matias B.</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>Heart, lung &amp; circulation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murphy, Alexandra C.</au><au>Koshy, Anoop N.</au><au>Farouque, Omar</au><au>Yeo, Belinda</au><au>Raman, Jaishankar</au><au>Kearney, Leighton</au><au>Yudi, Matias B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factor Xa Inhibition for the Treatment of Venous Thromboembolism Associated With Cancer: A Meta-Analysis of the Randomised Controlled Trials</atitle><jtitle>Heart, lung &amp; circulation</jtitle><addtitle>Heart Lung Circ</addtitle><date>2022-05</date><risdate>2022</risdate><volume>31</volume><issue>5</issue><spage>716</spage><epage>725</epage><pages>716-725</pages><issn>1443-9506</issn><eissn>1444-2892</eissn><abstract>Venous thromboembolism (VTE) is a common cause of morbidity and mortality in cancer patients. Until recently, guidelines recommended the use of low-molecular weight heparin (LMWH) as standard of care for VTE in patients with cancer. Despite the proven efficacy of direct oral anticoagulants (DOACs) for treatment of VTE, there is equipoise supporting their use in cancer patients. A systematic review of PubMed, Medline and EMBASE identified four randomised controlled trials (RCTs) in patients with cancer and VTE comparing a factor Xa inhibitor (FXaI) to LMWH. A meta-analysis was performed with a primary outcome of VTE recurrence and key secondary outcomes of major bleeding, clinically relevant non-major bleeding (CRNMB) and gastrointestinal (GI) bleeding. Four RCTs with 2,907 patients were included. 1,451 patients were randomised to FXaI and 1,456 to LMWH. VTE recurrence was lower in the FXaI group (RR 0.62, 95%CI 0.44–0.87; p=0.01; I2=24.90), with an absolute risk difference of -4% equating to a number needed to treat of 25 for prevention of recurrent VTE with FXaI. No significant difference in major bleeding was noted between groups (RR 1.33, 95%CI 0.84–2.11; p=0.23). Rates of GI bleeding (RR 1.87, 95%CI 1.06–3.29; p=0.03) and CRNMB (RR 1.57, 95%CI 1.11–2.23; p=0.01) were greater with FXaIs. In patients with cancer and VTE, the rate of VTE recurrence was significantly lower with FXaI than with LMWH without an increased risk of major bleeding. Our data supports the use of FXaIs as the standard of care for the treatment of VTE in this population.</abstract><cop>Australia</cop><pub>Elsevier B.V</pub><pmid>34896013</pmid><doi>10.1016/j.hlc.2021.10.024</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2821-1451</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1443-9506
ispartof Heart, lung & circulation, 2022-05, Vol.31 (5), p.716-725
issn 1443-9506
1444-2892
language eng
recordid cdi_proquest_miscellaneous_2609458685
source MEDLINE; Elsevier ScienceDirect Journals
subjects Anticoagulants - therapeutic use
Anticoagulation
Cancer
Cardio-oncology
Direct oral anticoagulation
Factor Xa
Factor Xa inhibitor
Factor Xa Inhibitors - therapeutic use
Fibrinolytic Agents
Hemorrhage - chemically induced
Heparin, Low-Molecular-Weight - therapeutic use
Humans
Low molecular weight heparin
Neoplasms - complications
Randomized Controlled Trials as Topic
Venous thromboembolism
Venous Thromboembolism - drug therapy
Venous Thromboembolism - etiology
title Factor Xa Inhibition for the Treatment of Venous Thromboembolism Associated With Cancer: A Meta-Analysis of the Randomised Controlled Trials
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T07%3A08%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Factor%20Xa%20Inhibition%20for%20the%20Treatment%20of%20Venous%20Thromboembolism%20Associated%20With%20Cancer:%20A%20Meta-Analysis%20of%20the%20Randomised%20Controlled%20Trials&rft.jtitle=Heart,%20lung%20&%20circulation&rft.au=Murphy,%20Alexandra%20C.&rft.date=2022-05&rft.volume=31&rft.issue=5&rft.spage=716&rft.epage=725&rft.pages=716-725&rft.issn=1443-9506&rft.eissn=1444-2892&rft_id=info:doi/10.1016/j.hlc.2021.10.024&rft_dat=%3Cproquest_cross%3E2609458685%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2609458685&rft_id=info:pmid/34896013&rft_els_id=S1443950621013494&rfr_iscdi=true