Anticoagulation for the initial treatment of venous thromboembolism in people with cancer
| dc.contributor.author | Hakoum, Maram B. | |
| dc.contributor.author | Kahale, Lara A. | |
| dc.contributor.author | Tsolakian, Ibrahim George | |
| dc.contributor.author | Matar, Charbel F. | |
| dc.contributor.author | Yosuico, Victor E.D. | |
| dc.contributor.author | Terrenato, Irene | |
| dc.contributor.author | Sperati, Francesca | |
| dc.contributor.author | Barba, Maddalena | |
| dc.contributor.author | Schunëmann, Holger J. | |
| dc.contributor.author | Akl, Elie A. | |
| dc.contributor.department | Family Medicine | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:42:22Z | |
| dc.date.available | 2025-01-24T11:42:22Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | Background: 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.doi | https://doi.org/10.1002/14651858.CD006649.pub7 | |
| dc.identifier.eid | 2-s2.0-85040927278 | |
| dc.identifier.pmid | 29363105 | |
| dc.identifier.uri | http://hdl.handle.net/10938/29977 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Ltd | |
| dc.relation.ispartof | Cochrane Database of Systematic Reviews | |
| dc.source | Scopus | |
| dc.subject | Anticoagulants | |
| dc.subject | Dalteparin | |
| dc.subject | Fibrinolytic agents | |
| dc.subject | Hemorrhage | |
| dc.subject | Heparin | |
| dc.subject | Heparin, low-molecular-weight | |
| dc.subject | Humans | |
| dc.subject | Neoplasms | |
| dc.subject | Polysaccharides | |
| dc.subject | Randomized controlled trials as topic | |
| dc.subject | Recurrence | |
| dc.subject | Secondary prevention | |
| dc.subject | Venous thromboembolism | |
| dc.subject | Antivitamin k | |
| dc.subject | Certoparin | |
| dc.subject | Coumarin | |
| dc.subject | Enoxaparin | |
| dc.subject | Fondaparinux | |
| dc.subject | Heparin calcium | |
| dc.subject | Nadroparin | |
| dc.subject | Reviparin | |
| dc.subject | Tinzaparin | |
| dc.subject | Warfarin | |
| dc.subject | Anticoagulant agent | |
| dc.subject | Fibrinolytic agent | |
| dc.subject | Low molecular weight heparin | |
| dc.subject | Polysaccharide | |
| dc.subject | All cause mortality | |
| dc.subject | Anticoagulant therapy | |
| dc.subject | Bleeding | |
| dc.subject | Chronic vein insufficiency | |
| dc.subject | Drug effect | |
| dc.subject | Drug efficacy | |
| dc.subject | Drug safety | |
| dc.subject | Human | |
| dc.subject | International normalized ratio | |
| dc.subject | Long term care | |
| dc.subject | Malignant neoplasm | |
| dc.subject | Outcome assessment | |
| dc.subject | Priority journal | |
| dc.subject | Quality of life | |
| dc.subject | Randomized controlled trial (topic) | |
| dc.subject | Recurrent disease | |
| dc.subject | Review | |
| dc.subject | Risk benefit analysis | |
| dc.subject | Systematic review | |
| dc.subject | Thrombocytopenia | |
| dc.subject | Chemically induced | |
| dc.subject | Complication | |
| dc.subject | Meta analysis | |
| dc.subject | Mortality | |
| dc.subject | Neoplasm | |
| dc.title | Anticoagulation for the initial treatment of venous thromboembolism in people with cancer | |
| dc.type | Review |
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