Abstract
Aims: Various drugs have recently been launched for the treatment of multiple myeloma (MM). This increase in the number of treatment options has potentially changed treatment patterns and medical costs for patients with MM. Japanese public health insurance claims were analyzed to examine the change in the treatment patterns of MM drugs and medical costs per patient.
Materials and methods: A claims database provided by Medical Data Vision was used, which includes data from ∼20 million patients from >300 acute care hospitals across Japan. The type of MM drugs prescribed and medical costs for patients with MM between April 2008 and December 2016 were examined using monthly cross-sectional analyses. Patients with an International Classification of Diseases, 10th Revision (ICD-10) diagnosis code of C90.0 were classified as having MM. MM drugs were defined by generic names.
Results: In total, 19,137 patients with MM (average age at first diagnosis: 69.6 years; percentage of women: 47.9%) were identified from the database. The percentage of patients prescribed each MM drug changed substantially as novel drugs were launched. Total medical costs increased until 2010, then stabilized. MM drug costs increased from approximately 2010, but costs for other care decreased, particularly for hospitalization (including surgery).
Limitations: The database contained data from large, acute care hospitals, which may have caused bias in terms of patients’ clinical history and disease severity.
Conclusions: Total medical costs for MM have remained stable since 2010. MM drug costs increased, but costs for other care decreased after the launch of lenalidomide in 2010 and other drugs in 2015 and later. More detailed research is required to confirm whether the launch of novel drugs caused the changes in medical costs.
Transparency
Declaration of funding
This study was funded by Celgene K.K.
Declaration of financial/other interests
SU and TO are employees of Celgene K.K. KI and TT are employees of Milliman, Inc., which has received consultancy fees from Celgene K.K. RG and KS have received advisory/lecture fees from Celgene K.K. JME peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Acknowledgements
We would like to thank Editage (www.editage.jp) for initial English language editing. We also wish to thank Saaya Tsutsue for helpful discussions. The authors received editorial assistance in the preparation of this manuscript from Rosie Morland, PhD, of Excerpta Medica, funded by Celgene Corporation. The authors are fully responsible for all content and editorial decisions for this manuscript.
Previous presentation
Parts of this study were presented at the 60th American Society of Hematology Annual Meeting & Exposition, December 1–4, 2018, San Diego, CA, USA.