Aspirin, Warfarin, or Enoxaparin Thromboprophylaxis in Patients With Multiple Myeloma Treated With Thalidomide: A Phase III, Open-Label, Randomized Trial

Antonio Palumbo(University of Bologna), Michèle Cavo(University of Bologna), Sara Bringhen(University of Bologna), Elena Zamagni(University of Bologna), Alessandra Romano(University of Bologna), Francesca Patriarca(University of Bologna), Davide Rossi(University of Bologna), Fabiana Gentilini(University of Bologna), Claudia Crippa(University of Bologna), Mónica Galli(University of Bologna), Chiara Nozzoli(University of Bologna), Roberto Ria(University of Bologna), Roberto Marasca(University of Bologna), Vittorio Montefusco(Fondazione IRCCS Istituto Nazionale dei Tumori), Luca Baldini(University of Bologna), Francesca Elice(University of Bologna), Vincenzo Callea(University of Bologna), Stefano Pulini(University of Bologna), Angelo Michele Carella(University of Bologna), Renato Zambello(University of Bologna), Giulia Benevolo(University of Bologna), Valeria Magarotto(University of Bologna), Paola Tacchetti(University of Bologna), Norbert Pescosta(University of Bologna), Claudia Cellini(University of Bologna), Claudia Polloni(University of Bologna), Andrea Evangelista(University of Bologna), Tommaso Caravita(University of Bologna), Fortunato Morabito(University of Bologna), Massimo Offidani(University of Bologna), Patrizia Tosi(University of Bologna), Mario Boccadoro(University of Bologna)
Journal of Clinical Oncology
February 1, 2011
Cited by 322Open Access
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Abstract

PURPOSE: In patients with myeloma, thalidomide significantly improves outcomes but increases the risk of thromboembolic events. In this randomized, open-label, multicenter trial, we compared aspirin (ASA) or fixed low-dose warfarin (WAR) versus low molecular weight heparin (LMWH) for preventing thromboembolism in patients with myeloma treated with thalidomide-based regimens. PATIENTS AND METHODS: A total of 667 patients with previously untreated myeloma who received thalidomide-containing regimens and had no clinical indication or contraindication for a specific antiplatelet or anticoagulant therapy were randomly assigned to receive ASA (100 mg/d), WAR (1.25 mg/d), or LMWH (enoxaparin 40 mg/d). A composite primary end point included serious thromboembolic events, acute cardiovascular events, or sudden deaths during the first 6 months of treatment. RESULTS: Of 659 analyzed patients, 43 (6.5%) had serious thromboembolic events, acute cardiovascular events, or sudden death during the first 6 months (6.4% in the ASA group, 8.2% in the WAR group, and 5.0% in the LMWH group). Compared with LMWH, the absolute differences were +1.3% (95% CI, -3.0% to 5.7%; P = .544) in the ASA group and +3.2% (95% CI, -1.5% to 7.8%; P = .183) in the WAR group. The risk of thromboembolism was 1.38 times higher in patients treated with thalidomide without bortezomib. Three major (0.5%) and 10 minor (1.5%) bleeding episodes were recorded. CONCLUSION: In patients with myeloma treated with thalidomide-based regimens, ASA and WAR showed similar efficacy in reducing serious thromboembolic events, acute cardiovascular events, and sudden deaths compared with LMWH, except in elderly patients where WAR showed less efficacy than LMWH.


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