Evidence map›Paper›PMID 41460360›Full record

ArticleClinical and experimental medicine2025

Finding appropriate timing for the combination of azathioprine and infliximab: propensity score matching and inverse probability of treatment weighting analysis.

Keke Tang, Yong Li, Ziheng Peng, Duo Xu, Yu Peng, Xiaowei Liu

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Article in Clinical and experimental medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Keke Tang *Department of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Yong Li *Department of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Ziheng PengDepartment of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Duo XuDepartment of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Yu PengDepartment of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. pengyu918@csu.edu.cn.ORCID http://orcid.org/0000-0001-6953-7816
Xiaowei LiuDepartment of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. liuxw@csu.edu.cn.ORCID http://orcid.org/0000-0002-1193-4277

Funding

National Natural Science Foundation of China 82070651National Natural Science Foundation of China 82230019
6 · The paper itself

Abstract

backgroundThe combination of azathioprine (AZA) with infliximab (IFX) enhances clinical efficacy in treating Crohn's disease (CD), increasing the risk of adverse events. This study aims to identify the optimal timing for AZA administration in IFX combination therapy to maximize patient benefit.

methodsThis was a retrospective, single-center study, which analyzed patients with CD undergoing IFX treatment from January 2017 to December 2022. Baseline data were collected. To minimize potential confounding effects, we utilized two established propensity score methods: propensity score matching (PSM) and inverse probability of treatment weighting (IPTW). The primary efficacy outcome was defined as the proportion of patients achieving clinical remission at the 54-week follow-up. Safety outcomes were evaluated through comprehensive monitoring and systematic classification of adverse events.

resultsA total of 528 active CD patients were included. Of these, 146 received concomitant AZA (AZA group), while 382 did not (non-AZA group). Following PSM or IPTW, the AZA group demonstrated significantly higher clinical remission rates (PSM: P < 0.001, IPTW: P < 0.001) compared to the non-AZA group. Furthermore, 46 patients used AZA during induction (IP-AZA group) and 100 during maintenance (MP-AZA group). After PSM or IPTW, both groups showed similar remission rates at 54 weeks (PSM: P = 0.793, IPTW: P = 0.508), with comparable safety profiles.

conclusionFor CD patients treated with IFX, whether AZA was initiated in the induction phase or during the maintenance phase, the impact on clinical outcomes and occurrence of adverse events was similar.

Indexed as

AzathioprineCrohn DiseaseImmunosuppressive AgentsInfliximabAdultDrug Therapy, CombinationFemaleHumansMaleMiddle AgedPropensity ScoreRemission InductionRetrospective StudiesTreatment OutcomeYoung AdultAzathioprineImmunosuppressive AgentsInfliximabAzathioprineCombination therapyCrohn’s diseaseInfliximab

Identifiers

PMID41460360
PMCPMC12774944

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.