Modelled Economic Analysis for Dacomitinib-A Cost Effectiveness Analysis in Treating Patients With EGFR-Mutation-Positive Non-Small Cell Lung Cancer in China

Yong-Feng Yu, Luan Luan, Fan-Fan Zhu, Peng Dong, Li-Heng Ma, Lan-Ting Li, Lan Gao, Shun Lu, Yong-Feng Yu, Luan Luan, Fan-Fan Zhu, Peng Dong, Li-Heng Ma, Lan-Ting Li, Lan Gao, Shun Lu

Abstract

Objectives: To establish the cost-effectiveness of dacomitinib compared to gefitinib from the Chinese healthcare system perspective.

Patients: Advanced non-small cell lung cancer (NSCLC) harbouring epidermal growth factor receptor (EGFR) mutations.

Methods: Partitioned survival analysis was undertaken to examine the cost-effectiveness of dacomitinib utilising individual patient data (IPD) from the pivotal randomised controlled trial (RCT) (ARCHER 1050). The three health states modelled were progression-free, post-progression, and death. Parametric survival distributions were fitted to IPD against the Kaplan-Meier survival curves corresponding to progression-free survival (PFS) and overall survival (OS) outcomes by randomised groups. Costs included drug acquisition and administration, outpatient management (outpatient consultation and examinations), and best supportive care costs. Utility weights were sourced from the pivotal trial and other published literature. The incremental cost-effectiveness ratio (ICER) was calculated with costs and quality-adjusted life years (QALYs) discounted at an annual rate of 5%. Both deterministic and probabilistic sensitivity analyses were undertaken.

Results: In the base case, dacomitinib (CNY 265,512 and 1.95 QALY) was associated with higher costs and QALY gains compared to gefitinib (CNY 247,048 and 1.61 QALYs), resulting in an ICER of CNY 58,947/QALY. Using the empirical WTP/QALY threshold, dacomitinib is a cost-effective treatment strategy for patients with EGFR-mutation-positive advanced NSCLC. The probabilistic sensitivity analysis suggested that dacomitinib had a 97% probability of being cost-effective.

Conclusions: Dacomitinib is a cost-effective treatment strategy in treating patients with EGFR-mutation-positive NSCLC from the Chinese healthcare system perspective. The uncertainty around the cost-effectiveness of dacomitinib could be reduced if long-term survival data become available.

Clinical trial registration: NCT01024413.

Keywords: NSCLC; cost-effectiveness analysis (CEA); economic model; epidermal growth factor receptor (EGFR) mutations; partitioned survival analysis.

Conflict of interest statement

LL, F-FZ, PD, and L-HM are employees of Pfizer China. L-TL was employed by Shanghai PalanDataRx Co., Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Copyright © 2021 Yu, Luan, Zhu, Dong, Ma, Li, Gao and Lu.

Figures

Figure 1
Figure 1
Parametric Fitting (Weibull) Compared to Observed KM Data: PFS (based on independent review committee) and OS for dacomitinib (upper) and gefitinib (lower). PFS, progression-free survival; OS, overall survival; KM, Kaplan-Meier.
Figure 2
Figure 2
Tornado diagram for the one-way sensitivity analysis. MRU, medical resource use; tx, treatment; OS, overall survival; PFS, progression-free survival; PPS, post-progression survival. The lower values were not tested for the dacomitinib OS parameters and its unit cost due to the negative ICER generated.
Figure 3
Figure 3
Incremental cost-effectiveness plane: Dacomitinib vs. gefitinib. The probability of dacomitinib being cost-effective is 97%.
Figure 4
Figure 4
Cost-effectiveness acceptability curve.

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Source: PubMed

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