Abstract
Objectives
Recognizing the value of anticancer treatments based on progression-free survival and overall survival may help decision making in healthcare policy. We aimed to measure and compare the impact of disease progression and terminal state prior to death on healthcare costs in HR+, HER2- ABC patients.
Methods
We conducted a retrospective study using Korean nationwide health insurance claims database between 1 September 2012 and 31 August 2017. The impact of disease progression was estimated by measuring the average incremental monthly cost per patient during 1 year after progression compared to 1 year before progression. Death-related costs per patient per month (PPPM) were measured for those who died within 1 year after progression. Generalized estimating equation (GEE) was used to estimate the variations in PPPM costs by progression and death with adjustment for clinical factors.
Results
After progression, 1,636 patients expensed $2,892 per month more on average than before progression ($3762 vs. $870). The GEE analysis with adjustment for baseline characteristics showed that PPPM costs increased by 3.46 folds (95% CI = 3.06–3.93) after progression. Also, PPPM costs were 1.74 (95%CI = 1.43–2.12) times higher in patients who died within 1 year after progression relative to survived patients. When considering the interaction between progression and death, deceased patients showed higher increased ratio of PPPM costs after progression (4.91; p=value<.0001) than survived patients (2.95; 95% CI = 2.61–3.34).
Conclusions
From the payer’s perspective, more healthcare costs incurred during the progression state than terminal state in HR+, HER2- ABC patients. The impact of disease progression emphasizes the importance of effectively treating HR+, HER2- ABC patients.
Transparency
Declaration of funding
This study was funded by Novartis.
Declaration of financial/other relationships
HK is an employee of Novartis. JAP, SYY, JYS, and SKP have no conflicts of interest to declare.
Author contributions
SKP, JAP, and HK contributed to conception and design of the study. SKP and JAP contributed to acquisition of data. SKP contributed to analysis and interpretation of data. SKP, JAP, SYY, and JYS contributed to drafting the article. All authors contributed to reviewing the article and approval of the final article.
Acknowledgements
The authors would like to thank Tae-Yong Kim, MD of Seoul National University Hospital for his expert advice and intellectual guidance in study design and Kayoung Jeong, MD of Novartis Korea for providing insightful suggestions in the data analysis.
Ethics approval and informed consent
This study was approved by `the Institutional Review Board (IRB) of Sungkyunkwan University (IRB File no. SKKU 2018-04-017-002). The claims data access was approved and provided by HIRA. Informed consent was waived by the IRB because HIRA claims data are anonymized and de-identified publicly available information.