PMID- 24945634 OWN - NLM STAT- MEDLINE DCOM- 20151002 LR - 20220310 IS - 1469-493X (Electronic) IS - 1361-6137 (Linking) IP - 6 DP - 2014 Jun 19 TI - Anticoagulation for the initial treatment of venous thromboembolism in patients with cancer. PG - CD006649 LID - 10.1002/14651858.CD006649.pub6 [doi] AB - BACKGROUND: Compared with patients without cancer, patients 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 patients with cancer. SEARCH METHODS: A comprehensive search for studies of anticoagulation in patients with cancer including a February 2013 electronic search of: the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, and ISI Web of Science. SELECTION CRITERIA: Randomized clinical trials (RCTs) comparing LMWH, UFH, and fondaparinux in patients with cancer and objectively confirmed VTE. DATA COLLECTION AND ANALYSIS: Using a standardized data form, review authors extracted data in duplicate on methodologic quality, participants, interventions, and outcomes of interest that included mortality, recurrent VTE, major bleeding, minor bleeding, postphlebitic syndrome, quality of life, and thrombocytopenia. MAIN RESULTS: Of 9559 identified citations, 16 RCTs were eligible: 13 compared LMWH with UFH, two compared fondaparinux with heparin, and one compared dalteparin with tinzaparin. Meta-analysis of 11 studies showed a statistically significant reduction in mortality at three months of follow-up with LMWH compared with UFH (risk ratio (RR) 0.71; 95% confidence interval (CI) 0.52 to 0.98). There was little change in the effect estimate after excluding studies of lower methodologic quality (RR 0.72; 95% CI 0.52 to 1.00). A meta-analysis of three studies comparing LMWH with UFH showed no statistically significant reduction in VTE recurrence (RR 0.78; 95% CI 0.29 to 2.08). The overall quality of evidence was low for LMWH versus UFH due to imprecision and likely publication bias. There were no statistically significant differences between heparin and fondaparinux for the outcomes of mortality (RR 1.27; 95% CI 0.88 to 1.84), recurrent VTE (RR 0.95; 95% CI 0.57 to 1.60), major bleeding (RR 0.79; 95% CI 0.39 to1.63), or minor bleeding (RR 1.50; 95% CI 0.87 to 2.59). The one study comparing dalteparin with tinzaparin found no statistically significant difference in mortality (RR 0.86; 95% CI 0.43 to 1.73). AUTHORS' CONCLUSIONS: LMWH is possibly superior to UFH in the initial treatment of VTE in patients with cancer. Additional trials focusing on patient-important outcomes will further inform the questions addressed in this review. FAU - Akl, Elie A AU - Akl EA AD - Department of Internal Medicine, American University of Beirut, Riad El Solh St, Beirut, Lebanon. FAU - Kahale, Lara AU - Kahale L FAU - Neumann, Ignacio AU - Neumann I FAU - Barba, Maddalena AU - Barba M FAU - Sperati, Francesca AU - Sperati F FAU - Terrenato, Irene AU - Terrenato I FAU - Muti, Paola AU - Muti P FAU - Schunemann, Holger AU - Schunemann H LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Review PT - Systematic Review DEP - 20140619 PL - England TA - Cochrane Database Syst Rev JT - The Cochrane database of systematic reviews JID - 100909747 RN - 0 (Anticoagulants) RN - 0 (Fibrinolytic Agents) RN - 0 (Heparin, Low-Molecular-Weight) RN - 0 (Polysaccharides) RN - 7UQ7X4Y489 (Tinzaparin) RN - 9005-49-6 (Heparin) RN - J177FOW5JL (Fondaparinux) RN - S79O08V79F (Dalteparin) SB - IM UOF - Cochrane Database Syst Rev. 2011;(6):CD006649. PMID: 21678360 UIN - Cochrane Database Syst Rev. 2018 Jan 24;1:CD006649. PMID: 29363105 MH - Anticoagulants/*therapeutic use MH - Dalteparin/therapeutic use MH - Fibrinolytic Agents/therapeutic use MH - Fondaparinux MH - Heparin/therapeutic use MH - Heparin, Low-Molecular-Weight/therapeutic use MH - Humans MH - Neoplasms/*complications MH - Polysaccharides/therapeutic use MH - Randomized Controlled Trials as Topic MH - Secondary Prevention MH - Tinzaparin MH - Venous Thromboembolism/*drug therapy/mortality EDAT- 2014/06/20 06:00 MHDA- 2015/10/03 06:00 CRDT- 2014/06/20 06:00 PHST- 2014/06/20 06:00 [entrez] PHST- 2014/06/20 06:00 [pubmed] PHST- 2015/10/03 06:00 [medline] AID - 10.1002/14651858.CD006649.pub6 [doi] PST - epublish SO - Cochrane Database Syst Rev. 2014 Jun 19;(6):CD006649. doi: 10.1002/14651858.CD006649.pub6.