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Oncology

Cost analysis for different sequential treatment regimens for metastatic renal cell carcinoma in China

, , , , , & show all
Pages 1150-1158 | Received 11 Jun 2018, Accepted 20 Aug 2018, Published online: 10 Sep 2018
 

Abstract

Purpose: Targeted therapies, including sunitinib, sorafenib, axitinib, and everolimus, have recently become the mainstay for the treatment of metastatic renal cell carcinoma (mRCC). The objective of this study was to estimate the costs of sequential treatment regimens for mRCC and associated adverse events (AEs) from the Chinese payers’ perspective.

Methods: Key inputs included in the calculation were patient population, dosing information, incidence rates and associated costs of Grade 3/4 AEs, treatment costs (including drug discount programs), and patients’ progression-free survival (PFS) as a proxy for length of treatment. To calculate PFS, this study identified pivotal clinical trials and generated a reconstructed individual patient data set from the published Kaplan-Meier survival curves. The median PFS from the pooled estimates were used in the calculation. In the base-case scenario, sunitinib was used as first line and the other three therapies were used as second line. Sensitivity analyses were conducted where (1) sorafenib was used as first line, or (2) a third-line therapy was added to the base-case scenario.

Results: In the base case, the cost per patient per treatment month (PPPM) cost was the lowest for sunitinib + axitinib among all sequential regimens (¥14,898) and was the highest for sunitinib + sorafenib (¥20,103). If sorafenib is used as first line, everolimus had lower per patient per months (PPPM) cost than axitinib (¥17,046 vs ¥23,337), but also had shorter PFS (13.5 months vs 15 months). Second sensitivity analysis with an additional third-line therapy showed consistent results with the base-case scenario; axitinib as second line was the least costly.

Conclusions: This study demonstrates that, for mRCC sequential treatment, sunitinib followed by axitinib generates the highest cost savings from the Chinese payers’ perspective. Future studies are warranted to examine the cost-effectiveness of various mRCC treatment regimens in Chinese populations.

JEL codes:

Transparency

Declaration of funding

This study was funded by Pfizer, Inc.

Declaration of financial/other relationships

HR and PD are employees of Pfizer, Inc. SHP, MX, and XG are/were employees of Pharmerit International, which has received consultancy fees from Pfizer, Inc. for this study. GS is an associate director of the Department of Urology at the Fudan University Shanghai Cancer Center and has been an advisor for Pfizer. XL is a surgeon at the Department of Urology at Fudan University Shanghai Cancer Center and has no relationships to declare. JME peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Author Contributions

All the authors contributed to study design, data analysis and interpretation, and manuscript development.

Ethics statement

All data are from publicly available sources without any approval requirement. According to Chinese regulations, this study does not require any IRB or ethics committee approval.

Acknowledgments

Medical writing assistance was provided by Catherine O’Connor, an employee of Pharmerit International.

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