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Feasibility of a Clinical Decision Support Tool for Ustekinumab to Predict Clinical Remission and Relapse in Patients With Crohn's Disease: A Multicenter Observational Study
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Park, Jihye | - |
| dc.contributor.author | Chun, Jaeyoung | - |
| dc.contributor.author | Yoon, Hyuk | - |
| dc.contributor.author | Cheon, Jae Hee | - |
| dc.date.accessioned | 2024-01-05T05:38:47Z | - |
| dc.date.available | 2024-01-05T05:38:47Z | - |
| dc.date.created | 2023-03-30 | - |
| dc.date.issued | 2023-04 | - |
| dc.identifier.issn | 1078-0998 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/197695 | - |
| dc.description.abstract | Background Ustekinumab was recently approved for the treatment of moderate to severe Crohn's disease (CD). Although the ustekinumab Clinical Decision Support Tool (UST-CDST) was able to predict ustekinumab responsiveness in a clinical trial, it is not clear whether UST-CDST can also predict a future clinical relapse following ustekinumab therapy in the real-life setting. Methods We enrolled patients with moderate to severe CD who were refractory to conventional therapies and who showed a clinical response after induction therapy with ustekinumab and monitored them until the relapse. We performed a Cox proportional hazard analysis to investigate the predictive capability of UST-CDST for a clinical disease relapse. Results Clinical remission rates at week 20 were 25.0% for low-probability responders, 66.7% for intermediate-probability responders, and 75.0% for high-probability responders. The high-probability responders were more likely to achieve clinical remission at week 20 compared with the low-probability responders. Among 99 patients with moderate to severe CD, 37 (37.4%) experienced a clinical relapse during the median follow-up period of 18.0 months of ustekinumab treatment. The cumulative relapse rates were 70.0% in the low-probability responders, 35.9% in the intermediate-probability responders, and 22.5% in the high-probability responders (P = .001). In a multivariable Cox proportional hazard analysis, the high-probability responders and intermediate-probability responders had a lower risk of clinical relapse than the low-probability responders. Receiver operating characteristic analysis using UST-CDST to predict relapse revealed an area under the curve of 0.698. Conclusions The UST-CDST can predict clinical relapse in patients with moderate to severe CD subjected to ustekinumab therapy. Lay Summary Clinical decision tools are useful in stratifying patients for optimal treatment. Here, we validate the capacity of Ustekinumab Clinical Decision Support Tool to predict clinical remission and relapse in Korean patients with moderate to severe Crohn's disease. | - |
| dc.description.statementOfResponsibility | restriction | - |
| dc.language | English | - |
| dc.publisher | Lippincott Williams & Wilkins | - |
| dc.relation.isPartOf | Inflammatory Bowel Diseases | - |
| dc.relation.isPartOf | INFLAMMATORY BOWEL DISEASES | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.title | Feasibility of a Clinical Decision Support Tool for Ustekinumab to Predict Clinical Remission and Relapse in Patients With Crohn's Disease: A Multicenter Observational Study | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Park, Jihye | - |
| dc.contributor.googleauthor | Chun, Jaeyoung | - |
| dc.contributor.googleauthor | Yoon, Hyuk | - |
| dc.contributor.googleauthor | Cheon, Jae Hee | - |
| dc.identifier.doi | 10.1093/ibd/izac105 | - |
| dc.relation.journalcode | J01060 | - |
| dc.identifier.eissn | 1536-4844 | - |
| dc.identifier.pmid | 35670522 | - |
| dc.subject.keyword | Crohn&apos | - |
| dc.subject.keyword | s disease | - |
| dc.subject.keyword | relapse | - |
| dc.subject.keyword | UST-CDST | - |
| dc.subject.keyword | ustekinumab | - |
| dc.contributor.alternativeName | Park, Ji Hye | - |
| dc.contributor.affiliatedAuthor | Park, Jihye | - |
| dc.contributor.affiliatedAuthor | Chun, Jaeyoung | - |
| dc.contributor.affiliatedAuthor | Cheon, Jae Hee | - |
| dc.identifier.scopusid | 2-s2.0-85136827577 | - |
| dc.identifier.wosid | 000807078300001 | - |
| dc.citation.volume | 29 | - |
| dc.citation.number | 4 | - |
| dc.citation.startPage | 548 | - |
| dc.citation.endPage | 554 | - |
| dc.identifier.bibliographicCitation | Inflammatory Bowel Diseases, Vol.29(4) : 548-554, 2023-04 | - |
| dc.identifier.rimsid | 78223 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Crohn&apos | - |
| dc.subject.keywordAuthor | s disease | - |
| dc.subject.keywordAuthor | relapse | - |
| dc.subject.keywordAuthor | UST-CDST | - |
| dc.subject.keywordAuthor | ustekinumab | - |
| dc.subject.keywordPlus | OUTCOMES | - |
| dc.subject.keywordPlus | EXPERIENCE | - |
| dc.type.docType | Article; Early Access | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Gastroenterology & Hepatology | - |
| dc.relation.journalResearchArea | Gastroenterology & Hepatology | - |
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