Cost-Effectiveness Analysis of Vedolizumab Compared With Infliximab in Anti-TNF-α-Naïve Patients With Moderate-to-Severe Ulcerative Colitis in China
- PMID: 34490187
- PMCID: PMC8417715
- DOI: 10.3389/fpubh.2021.704889
Cost-Effectiveness Analysis of Vedolizumab Compared With Infliximab in Anti-TNF-α-Naïve Patients With Moderate-to-Severe Ulcerative Colitis in China
Abstract
Objective: To evaluate the cost effectiveness of vedolizumab vs. infliximab in the treatment of anti-tumor necrosis factor-alpha (TNF-α)-naïve patients with moderate-to-severe active ulcerative colitis (UC) in China. Methods: The costs and effectiveness of vedolizumab and infliximab in the treatment of anti-TNF-α naïve patients with moderate-to-severe active UC were compared using a hybrid decision tree model and a Markov model. From the perspective of the Chinese healthcare system, this study simulated the lifetime health benefits [quality-adjusted life-years (QALYs)] and costs (USD) for patients with UC from the induction phase to the maintenance phase, with an annual discount rate of 5%. The clinical efficacy and transition probability data were based on a previously published network meta-analysis. The health utility, surgical risk, biologic drug discontinuation rate, and mortality were derived from previous literature and the Chinese statistical yearbook. The cost data were based on China's drug purchase and biding platform and the results of a survey sent to clinicians in 18 tertiary hospitals. One-way and probabilistic sensitivity analyses (PSAs) were performed to validate the robustness of the models' assumptions and specific parameter estimates. Results: The results of the base-case analyses showed that compared with infliximab, vedolizumab led to a gain of 0.25 QALYs (9.56 vs. 9.31 QALYs) and was less expensive by $7,349 ($180,138 vs. 187,487), indicating that the use of vedolizumab was a dominant strategy. The results of one-way sensitivity analyses suggested that the annual discount rate and health-state costs had the greatest impact, but the results were otherwise consistent with those of the base-case analyses. The PSAs suggested that vedolizumab had a 98.6% probability of being effective at a threshold of 3 times the gross domestic product (GDP) per capita in China in 2020. Conclusion: Compared with infliximab, vedolizumab appears to be a more cost-effective option in the treatment of anti-TNF-α naïve adult patients with moderate-to-severe, active UC in China.
Keywords: China; cost-effectiveness analysis; infliximab; ulcerative colitis; vedolizumab.
Copyright © 2021 Zhou, Sheng, Guan, Meng and Wang.
Conflict of interest statement
YS is an employee of Takeda (China) International Trading 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.
Figures



Similar articles
-
Cost-Effectiveness Analysis of Vedolizumab Compared with Other Biologics in Anti-TNF-Naïve Patients with Moderate-to-Severe Ulcerative Colitis in Japan.Pharmacoeconomics. 2020 Jan;38(1):69-84. doi: 10.1007/s40273-019-00841-1. Pharmacoeconomics. 2020. PMID: 31552601 Free PMC article.
-
Cost-Effectiveness of Vedolizumab in the Treatment of Moderate-to-Severe Crohn's Disease in China.Adv Ther. 2021 Aug;38(8):4233-4245. doi: 10.1007/s12325-021-01806-7. Epub 2021 Jun 5. Adv Ther. 2021. PMID: 34089502 Free PMC article.
-
Identification of the Most Cost-effective Position of Vedolizumab Among the Available Biologic Drugs for the Treatment of Ulcerative Colitis.J Crohns Colitis. 2020 Jun 19;14(5):575-587. doi: 10.1093/ecco-jcc/jjz212. J Crohns Colitis. 2020. PMID: 31901085 Free PMC article.
-
Vedolizumab for Treating Moderately to Severely Active Crohn's Disease After Prior Therapy: An Evidence Review Group Perspective of a NICE Single Technology Appraisal.Pharmacoeconomics. 2016 Dec;34(12):1241-1253. doi: 10.1007/s40273-016-0436-6. Pharmacoeconomics. 2016. PMID: 27480631 Review.
-
Cost utility of tumour necrosis factor-α inhibitors for rheumatoid arthritis: an application of Bayesian methods for evidence synthesis in a Markov model.Pharmacoeconomics. 2012 Jul 1;30(7):575-93. doi: 10.2165/11594990-000000000-00000. Pharmacoeconomics. 2012. PMID: 22640174 Review.
Cited by
-
Pharmacokinetic and safety profiles of mesalazine enema in healthy Chinese subjects: A single- and multiple-dose study.PLoS One. 2024 Feb 2;19(2):e0296940. doi: 10.1371/journal.pone.0296940. eCollection 2024. PLoS One. 2024. PMID: 38306390 Free PMC article. Clinical Trial.
-
Cost Effectiveness of Sequencing Vedolizumab as First-Line Biologic in Ulcerative Colitis and Crohn's Disease in Canada: An Analysis Using Real-World Evidence from the EVOLVE Study.Pharmacoecon Open. 2025 Jan;9(1):41-56. doi: 10.1007/s41669-024-00523-5. Epub 2024 Oct 8. Pharmacoecon Open. 2025. PMID: 39377864 Free PMC article.
-
Effectiveness and cost-effectiveness of an integrated digital psychological intervention (EmoEase) in Chinese chronic obstructive pulmonary disease patients: Study protocol of a randomized controlled trial.Digit Health. 2024 Oct 1;10:20552076241277650. doi: 10.1177/20552076241277650. eCollection 2024 Jan-Dec. Digit Health. 2024. PMID: 39381816 Free PMC article.
-
Development and Initial Use of a New Inflammatory Bowel Disease Clinical Database Integrating Both Eastern and Western Clinical Characteristics.Chronic Dis Transl Med. 2025 Feb 14;11(2):130-139. doi: 10.1002/cdt3.70000. eCollection 2025 Jun. Chronic Dis Transl Med. 2025. PMID: 40486950 Free PMC article.
-
Sponsorship bias in published pharmacoeconomic evaluations of national reimbursement negotiation drugs in China: a systematic review.BMJ Glob Health. 2023 Nov 29;8(11):e012780. doi: 10.1136/bmjgh-2023-012780. BMJ Glob Health. 2023. PMID: 38030227 Free PMC article.
References
-
- GBD 2017 Inflammatory Bowel Disease Collaborators. The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. (2020) 5:17–30. 10.1016/S2468-1253(19)30333-4 - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical