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

Author:

Seefat M. R.1ORCID,Cucchi D. G. J.12ORCID,Groen K.1,Donker M. L.1,van der Hem K. G.3,Westerman M.4,Gerrits A. M.5,Beeker A.6,van de Donk N. W. C. J.1ORCID,Blommestein H. M.7ORCID,Zweegman S.1ORCID

Affiliation:

1. Department of Hematology Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Cancer Center Amsterdam Amsterdam The Netherlands

2. Department of Internal Medicine Franciscus Gasthuis & Vlietland Rotterdam The Netherlands

3. Department of Internal Medicine Zaandam Medical Center Zaandam The Netherlands

4. Department of Internal Medicine Northwest Clinics Alkmaar The Netherlands

5. Department of Internal Medicine OLVG Amsterdam The Netherlands

6. Department of Internal Medicine Spaarne Gasthuis Hoofddorp The Netherlands

7. Erasmus School of Health Policy and Management Erasmus University Rotterdam Rotterdam The Netherlands

Abstract

AbstractNovel 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.

Publisher

Wiley

Subject

Hematology,General Medicine

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