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The incidence of thromboembolism for lenalidomide versus thalidomide in older patients with newly diagnosed multiple myeloma

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Abstract

It is uncertain if different immunomodulatory drugs (IMID) pose distinct thrombotic risk in patients with newly diagnosed multiple myeloma (MM). Among 2397 MM patients from the SEER-Medicare database from 2007 to 2013, 78% received lenalidomide, and 22% received thalidomide. After inverse probability weighting to balance confounders, the 12-month incidences of venous thromboembolism (VTE 10%) and arterial thromboembolism (ATE 5%) were similarly high in both groups. Lenalidomide versus thalidomide had a subdistribution hazard ratio of 1.11 (0.59–2.02) for VTE and a subdistribution hazard ratio of 0.96 (0.45–1.98) for ATE. Overall survival was not significantly different with a hazard ratio of 0.88 (0.60–1.18) for lenalidomide versus thalidomide. Concurrent anticoagulant prophylaxis was infrequently prescribed in < 20% of both groups. Our study demonstrates that despite improvement in myeloma-directed therapy and supportive care, thrombosis remains an important consideration for all IMID-treated MM patients. Appropriate risk stratification and vigilant thromboprophylaxis remain essential to prevent this complication.

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Acknowledgments

AL performed the research, designed the study, analyzed the data, and wrote the paper. DAG and GHL performed the research, designed the study, and wrote the paper. QW and GW analyzed the data. SL and ENL contributed essential tools and wrote the paper.

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Correspondence to Ang Li.

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Conflict of interest

The current study itself was conducted without funding from industry. AL reports grant funding from the Conquer Cancer Foundation Young Investigator Award, Hemostasis and Thrombosis Research Society Mentored Research Award supported by an independent medical educational grant from Shire, and National Hemophilia Foundation Shire Clinical Fellowship Award. Other authors report no relevant financial interests, activities, relationships, or affiliations.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

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Informed consent was not obtained because this was a de-identified aggregate national claims database study where individual patient could not be identified and informed consent could not be obtained. The study was reviewed and considered exempt by the University of Washington Institutional Review Board.

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Li, A., Wu, Q., Warnick, G. et al. The incidence of thromboembolism for lenalidomide versus thalidomide in older patients with newly diagnosed multiple myeloma. Ann Hematol 99, 121–126 (2020). https://doi.org/10.1007/s00277-019-03860-2

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