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Prevention of thalidomide- and lenalidomide-associated thrombosis in myeloma

  • A. Palumbo
  • , S. V. Rajkumar
  • , M. A. Dimopoulos
  • , P. G. Richardson
  • , J. San Miguel
  • , B. Barlogie
  • , J. Harousseau
  • , J. A. Zonder
  • , M. Cavo
  • , M. Zangari
  • , M. Attal
  • , A. Belch
  • , S. Knop
  • , D. Joshua
  • , O. Sezer
  • , H. Ludwig
  • , D. Vesole
  • , J. Bladé
  • , R. Kyle
  • , J. Westin
  • D. Weber, S. Bringhen, R. Niesvizky, A. Waage, M. von Lilienfeld-Toal, S. Lonial, G. J. Morgan, R. Z. Orlowski, K. Shimizu, K. C. Anderson, M. Boccadoro, B. G. Durie, P. Sonneveld, M. A. Hussein
  • University of Turin
  • Mayo Clinic Rochester, MN
  • National and Kapodistrian University of Athens
  • Dana-Farber Cancer Institute
  • Hospital Clínico Universitario de Salamanca
  • University of Arkansas for Medical Sciences
  • University Hospital Hotel-Dieu
  • Wayne State University
  • University of Bologna
  • CHU de Toulouse
  • Cross Cancer Institute
  • University of Tübingen
  • Royal Prince Alfred Hospital
  • Charité – Universitätsmedizin Berlin
  • Klinik Ottakring
  • University of Barcelona
  • Mayo Clinic College of Medicine and Science
  • Lund University
  • University of Texas MD Anderson Cancer Center
  • Cornell University
  • Norwegian University of Science and Technology
  • Leeds Teaching Hospitals NHS Trust
  • Emory University
  • Royal Marsden NHS Foundation Trust
  • University of North Carolina at Chapel Hill
  • Nagoya City Midori General Hospital
  • Cedars-Sinai Medical Center
  • Erasmus University Rotterdam
  • Cleveland Clinic Foundation

Research output: Contribution to journal › Article › peer-review

804 Scopus citations

Abstract

The incidence of venous thromboembolism (VTE) is more than 1‰ annually in the general population and increases further in cancer patients. The risk of VTE is higher in multiple myeloma (MM) patients who receive thalidomide or lenalidomide, especially in combination with dexamethasone or chemotherapy. Various VTE prophylaxis strategies, such as low-molecular-weight heparin (LMWH), warfarin or aspirin, have been investigated in small, uncontrolled clinical studies. This manuscript summarizes the available evidence and recommends a prophylaxis strategy according to a risk-assessment model. Individual risk factors for thrombosis associated with thalidomide/lenalidomide-based therapy include age, history of VTE, central venous catheter, comorbidities (infections, diabetes, cardiac disease), immobilization, surgery and inherited thrombophilia. Myeloma-related risk factors include diagnosis and hyperviscosity. VTE is very high in patients who receive high-dose dexamethasone, doxorubicin or multiagent chemotherapy in combination with thalidomide or lenalidomide, but not with bortezomib. The panel recommends aspirin for patients with ≤1 risk factor for VTE. LMWH (equivalent to enoxaparin 40mg per day) is recommended for those with two or more individual/myeloma-related risk factors. LMWH is also recommended for all patients receiving concurrent high-dose dexamethasone or doxorubicin. Full-dose warfarin targeting a therapeutic INR of 2-3 is an alternative to LMWH, although there are limited data in the literature with this strategy. In the absence of clear data from randomized studies as a foundation for recommendations, many of the following proposed strategies are the results of common sense or derive from the extrapolation of data from many studies not specifically designed to answer these questions. Further investigation is needed to define the best VTE prophylaxis.

Original languageEnglish
Pages (from-to)414-423
Number of pages10
JournalLeukemia
Volume22
Issue number2
DOIs
StatePublished - Feb 2008

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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