论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
Authors Huang J, Liao W, Zhou J, Zhang P, Wen F, Wang X, Zhang M, Zhou K, Wu Q, Li Q
Received 30 April 2018
Accepted for publication 24 July 2018
Published 1 October 2018 Volume 2018:10 Pages 4065—4072
DOI https://doi.org/10.2147/CMAR.S172704
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Cristina Weinberg
Peer reviewer comments 2
Editor who approved publication: Professor Nakshatri
Background: The effectiveness of gemcitabine plus capecitabine compared with
gemcitabine monotherapy for resected pancreatic cancer has been evaluated in
the ESPAC-4 trial. We aimed to assess the cost-effectiveness of these adjuvant
regimens on resected pancreatic cancer.
Methods: A Markov model was established to simulate the disease process of
resected pancreatic cancer (relapse-free survival, progressive disease, and
death). The efficacy and toxicity profiles were collected from the ESPAC-4
trial. Transition probabilities were calculated based on survival in each
group. Cost data were calculated from the perspective of the Chinese healthcare
payer. The primary endpoint in the analysis was the incremental
cost-effectiveness ratio (ICER), and model uncertainties were explored by
one-way sensitivity analysis and probabilistic sensitivity analysis.
Results: Our results demonstrated that gemcitabine monotherapy cost
$36,028.45 and yielded a survival of 1.02 quality-adjusted life year (QALY),
while gemcitabine plus capecitabine cost $46,095.05 and yielded a survival of
1.23 QALY. Therefore, the incremental cost-effectiveness ratio of gemcitabine
plus capecitabine vs gemcitabine monotherapy was $45,191.23 which surpassed the
willingness-to-pay threshold of $29,291.42 per QALY in China.
Conclusion: The gemcitabine monotherapy regimen is more cost-effective
compared with gemcitabine plus capecitabine regimen for the patients with
postoperative pancreatic cancer from the Chinese societal perspective.
Keywords: cost-effectiveness, Markov model, gemcitabine, capecitabine,
resected pancreatic cancer