Assessing the risk of venous thromboembolism in multiple myeloma

Kristen M Sanfilippo1

  • 1Division of Hematology/Oncology, Veterans Administration St. Louis Health Care System, St. Louis, Missouri, USA; Division of Hematology, Washington University School of Medicine, St. Louis, Missouri, USA.

Thrombosis Research
|August 2, 2020
PubMed

Insights

Patients with multiple myeloma face a high risk of venous thromboembolism (VTE), especially within the first year of diagnosis. Primary thromboprophylaxis may reduce VTE risk and improve outcomes in these patients.

Area of Science:

  • Hematology
  • Oncology
  • Thrombosis Research

Background:

  • Multiple myeloma (MM) patients exhibit elevated venous thromboembolism (VTE) risk compared to the general population.
  • VTE development in MM is linked to poorer patient outcomes, including increased mortality.
  • Current thromboprophylaxis studies often exclude high-risk MM patients.

Purpose of the Study:

  • To evaluate the potential of primary thromboprophylaxis in reducing VTE risk and improving outcomes for multiple myeloma patients.
  • To review existing risk prediction scores for VTE in MM and explore the role of biomarkers.

Main Methods:

  • Analysis of meta-analyses on primary thromboprophylaxis in ambulatory cancer patients at high VTE risk.
  • Review of current clinical risk prediction scores for VTE in MM: IMWG/NCCN, SAVED, and IMPEDE VTE.
  • Discussion of the potential role of biomarkers in enhancing VTE risk prediction.

Main Results:

  • Meta-analysis showed VTE risk reduction with prophylaxis in high-risk cancer patients, without increased major bleeding.
  • The SAVED and IMPEDE VTE scores demonstrate superior performance in predicting VTE in MM compared to the IMWG/NCCN score.
  • Biomarkers hold promise for improving VTE risk prediction accuracy in MM.

Conclusions:

  • Primary thromboprophylaxis is a potential strategy to mitigate VTE risk in multiple myeloma.
  • Enhanced VTE risk prediction in MM may be achieved by integrating biomarkers with existing clinical scores.
  • Further research is warranted to validate biomarker-enhanced risk scores for VTE in MM.

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