Cost-effectiveness Analysis of Pembrolizumab in Combination with Chemotherapy Compared with Chemotherapy Alone As First-line Treatment for Patients with Advanced Biliary Tract Cancer in China
Overview
Authors
Affiliations
Objective: The objective of this study is to evaluate the cost-effectiveness of adding pembrolizumab to the standard first-line therapy of advanced biliary tract cancer (BTC) with gemcitabine and cisplatin from the perspective of the Chinese healthcare system.
Methods: The partitioned survival model developed from clinical data obtained in The KEYNOTE-966 trial served as the basis for a simulation in the TreeAge Pro 2011 software. The objective of the research was to estimate the 10-year life expectancy and total healthcare costs of patients with BTC, utilizing primary outcomes that evaluated costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratio (ICER). To establish the willingness-to-pay (WTP) threshold, the 2022 Chinese per capita gross domestic product (GDP) of $37304.346/QALY was adopted. Furthermore, sensitivity analysis was conducted to ascertain the study's results under varying levels of uncertainty.
Results: Compared to chemotherapy alone, the addition of pembrolizumab to chemotherapy has been shown to yield an incremental gain of 0.184 quality-adjusted life years (QALY) at an additional cost of $103940.706. This translates into an incremental cost-effectiveness ratio (ICER) of $564895.141/QALY, which exceeds the willingness-to-pay (WTP) threshold in China. One-way sensitivity analyses performed on the model recognize the utility of PD, subsequent cost, and the cost of Pembrolizumab 100 mg had a major influence on the outcomes. However, no parameter elicited an ICER lower than the willingness-to-pay (WTP) threshold.
Conclusions: Based on the perspective of the Chinese healthcare system, the utilization of pembrolizumab in combination with chemotherapy as an first-line treatment option for BTC does not appear to be a cost-effective approach compared to chemotherapy as a standalone therapy.
Liu R, Zhao Y, Shi F, Zhu J, Wu J, Huang M Immunotherapy. 2024; 16(10):669-678.
PMID: 39259510 PMC: 11404697. DOI: 10.1080/1750743X.2024.2347822.
Kashiwa M, Maeda H J Gastrointest Cancer. 2024; 55(4):1569-1580.
PMID: 39172318 DOI: 10.1007/s12029-024-01106-7.
Mauro E, Sanduzzi-Zamparelli M, Sauri T, Soler A, Iserte G, Fortuny M Cancers (Basel). 2024; 16(11).
PMID: 38893196 PMC: 11171222. DOI: 10.3390/cancers16112077.
Ma Y, Pan Y, Li Y, Guan H, Dai G J Cancer Res Clin Oncol. 2024; 150(5):247.
PMID: 38722378 PMC: 11081983. DOI: 10.1007/s00432-024-05771-w.