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Treatment sequences and drug costs from diagnosis to death in multiple myeloma

  • Amsterdam UMC
  • Department of Oncology, Franciscus Gasthuis & Vlietland, Rotterdam, the Netherlands
  • Department of Trauma Surgery, Zaandam Medical Center, Zaandam, The Netherlands
  • Zaandam Medical Center
  • North West Hospital Group
  • Onze Lieve Vrouwe Gasthuis
  • Division of Molecular Internal Medicine, Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Spaarne Gasthuis
  • Erasmus School of Health Policy & Management
  • Department of Health Technology Assessment, Erasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, the Netherlands; Institute for Medical Technology Assessment, Erasmus University Rotterdam, Rotterdam, the Netherlands.

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Novel therapies for multiple myeloma (MM) have improved patient survival, but their high costs strain healthcare budgets. End-of-life phases of treatment are generally the most expensive, however, these high costs may be less justifiable in the context of a less pronounced clinical benefit. To manage drug expenses effectively, detailed information on end-of-life drug administration and costs are crucial. In this retrospective study, we analysed treatment sequences and drug costs from 96 MM patients in the Netherlands who died between January 2017 and July 2019. Patients received up to 16 lines of therapy (median overall survival: 56.5 months), with average lifetime costs of €209 871 (€3111/month; range: €3942–€776 185) for anti-MM drugs. About 85% of patients received anti-MM treatment in the last 3 months before death, incurring costs of €20 761 (range: €70–€50 122; 10% of total). Half of the patients received anti-MM treatment in the last 14 days, mainly fully oral regimens (66%). End-of-life treatment costs are substantial despite limited survival benefits. The use of expensive treatment options is expected to increase costs further. These data serve as a reference point for future cost studies, and further research is needed to identify factors predicting the efficacy and clinical benefit of continuing end-of-life therapy.
Original languageEnglish
Pages (from-to)360-366
Number of pages7
JournalEuropean journal of haematology
Volume112
Issue number3
Early online date11 Oct 2023
DOIs
Publication statusPublished - 1 Mar 2024

Keywords

  • clinical practice
  • cost
  • cost-effectiveness
  • end-of-life
  • multiple myeloma
  • terminal
  • treatment

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