Anticoagulation for the initial treatment of venous thromboembolism in people with cancer

dc.contributor.authorHakoum, Maram B.
dc.contributor.authorKahale, Lara A.
dc.contributor.authorTsolakian, Ibrahim George
dc.contributor.authorMatar, Charbel F.
dc.contributor.authorYosuico, Victor E.D.
dc.contributor.authorTerrenato, Irene
dc.contributor.authorSperati, Francesca
dc.contributor.authorBarba, Maddalena
dc.contributor.authorSchunëmann, Holger J.
dc.contributor.authorAkl, Elie A.
dc.contributor.departmentFamily Medicine
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:42:22Z
dc.date.available2025-01-24T11:42:22Z
dc.date.issued2018
dc.description.abstractBackground: Compared with people without cancer, people with cancer who receive anticoagulant treatment for venous thromboembolism (VTE) are more likely to develop recurrent VTE. Objectives: To compare the efficacy and safety of three types of parenteral anticoagulants (i.e. fixed-dose low molecular weight heparin (LMWH), adjusted-dose unfractionated heparin (UFH), and fondaparinux) for the initial treatment of VTE in people with cancer. Search methods: A comprehensive search included a major electronic search of the following databases: Cochrane Central Register of Controlled Trials (CENTRAL) (2018, Issue 1), MEDLINE (via Ovid) and Embase (via Ovid); handsearching of conference proceedings; checking of references of included studies; use of the 'related citation' feature in PubMed; and a search for ongoing studies. This update of the systematic review was based on the findings of a literature search conducted on 14 January 2018. Selection criteria: Randomized controlled trials (RCTs) assessing the benefits and harms of LMWH, UFH, and fondaparinux in people with cancer and objectively confirmed VTE. Data collection and analysis: Using a standardized form, we extracted data in duplicate on study design, participants, interventions outcomes of interest, and risk of bias. Outcomes of interested included all-cause mortality, symptomatic VTE, major bleeding, minor bleeding, postphlebitic syndrome, quality of life, and thrombocytopenia. We assessed the certainty of evidence for each outcome using the GRADE approach. Main results: Of 15440 identified citations, 7387 unique citations, 15 RCTs fulfilled the eligibility criteria. These trials enrolled 1615 participants with cancer and VTE: 13 compared LMWH with UFH enrolling 1025 participants, one compared fondaparinux with UFH and LMWH enrolling 477 participants, and one compared dalteparin with tinzaparin enrolling 113 participants. The meta-analysis of mortality at three months included 418 participants from five studies and that of recurrent VTE included 422 participants from 3 studies. The findings showed that LMWH likely decreases mortality at three months compared to UFH (risk ratio (RR) 0.66, 95% confidence interval (CI) 0.40 to 1.10; risk difference (RD) 57 fewer per 1000, 95% CI 101 fewer to 17 more; moderate certainty evidence), but did not rule out a clinically significant increase or decrease in VTE recurrence (RR 0.69, 95% CI 0.27 to 1.76; RD 30 fewer per 1000, 95% CI 70 fewer to 73 more; moderate certainty evidence). The study comparing fondaparinux with heparin (UFH or LMWH) did not exclude a beneficial or detrimental effect of fondaparinux on mortality at three months (RR 1.25, 95% CI 0.86 to 1.81; RD 43 more per 1000, 95% CI 24 fewer to 139 more; moderate certainty evidence), recurrent VTE (RR 0.93, 95% CI 0.56 to 1.54; RD 8 fewer per 1000, 95% CI 52 fewer to 63 more; moderate certainty evidence), major bleeding (RR 0.82, 95% CI 0.40 to 1.66; RD 12 fewer per 1000, 95% CI 40 fewer to 44 more; moderate certainty evidence), or minor bleeding (RR 1.53, 95% CI 0.88 to 2.66; RD 42 more per 1000, 95% CI 10 fewer to 132 more; moderate certainty evidence) The study comparing dalteparin with tinzaparin did not exclude a beneficial or detrimental effect of dalteparin on mortality (RR 0.86, 95% CI 0.43 to 1.73; RD 33 fewer per 1000, 95% CI 135 fewer to 173 more; low certainty evidence), recurrent VTE (RR 0.44, 95% CI 0.09 to 2.16; RD 47 fewer per 1000, 95% CI 77 fewer to 98 more; low certainty evidence), major bleeding (RR 2.19, 95% CI 0.20 to 23.42; RD 20 more per 1000, 95% CI 14 fewer to 380 more; low certainty evidence), or minor bleeding (RR 0.82, 95% CI 0.30 to 2.21; RD 24 fewer per 1000, 95% CI 95 fewer to 164 more; low certainty evidence). Authors' conclusions: LMWH is possibly superior to UFH in the initial treatment of VTE in people with cancer. Additional trials focusing on patient-important outcomes will further inform the questions addressed in this review. The decision for a person with cancer to start LMWH therapy should balance the benefits and harms and consider the person's values and preferences. © 2018 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
dc.identifier.doihttps://doi.org/10.1002/14651858.CD006649.pub7
dc.identifier.eid2-s2.0-85040927278
dc.identifier.pmid29363105
dc.identifier.urihttp://hdl.handle.net/10938/29977
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.ispartofCochrane Database of Systematic Reviews
dc.sourceScopus
dc.subjectAnticoagulants
dc.subjectDalteparin
dc.subjectFibrinolytic agents
dc.subjectHemorrhage
dc.subjectHeparin
dc.subjectHeparin, low-molecular-weight
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectPolysaccharides
dc.subjectRandomized controlled trials as topic
dc.subjectRecurrence
dc.subjectSecondary prevention
dc.subjectVenous thromboembolism
dc.subjectAntivitamin k
dc.subjectCertoparin
dc.subjectCoumarin
dc.subjectEnoxaparin
dc.subjectFondaparinux
dc.subjectHeparin calcium
dc.subjectNadroparin
dc.subjectReviparin
dc.subjectTinzaparin
dc.subjectWarfarin
dc.subjectAnticoagulant agent
dc.subjectFibrinolytic agent
dc.subjectLow molecular weight heparin
dc.subjectPolysaccharide
dc.subjectAll cause mortality
dc.subjectAnticoagulant therapy
dc.subjectBleeding
dc.subjectChronic vein insufficiency
dc.subjectDrug effect
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectHuman
dc.subjectInternational normalized ratio
dc.subjectLong term care
dc.subjectMalignant neoplasm
dc.subjectOutcome assessment
dc.subjectPriority journal
dc.subjectQuality of life
dc.subjectRandomized controlled trial (topic)
dc.subjectRecurrent disease
dc.subjectReview
dc.subjectRisk benefit analysis
dc.subjectSystematic review
dc.subjectThrombocytopenia
dc.subjectChemically induced
dc.subjectComplication
dc.subjectMeta analysis
dc.subjectMortality
dc.subjectNeoplasm
dc.titleAnticoagulation for the initial treatment of venous thromboembolism in people with cancer
dc.typeReview

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