1 1

Cited 0 times in

Cited 0 times in

Effectiveness and Tolerability of Anti-Tumor Necrosis Factor Alpha Therapy in Refractory Intestinal Behçet's Disease: A Large Single-Center Study

DC Field Value Language
dc.contributor.authorChang, Ji Young-
dc.contributor.authorKim, Jiwoo-
dc.contributor.authorPark, Soo Jung-
dc.contributor.authorPark, Jae Jun-
dc.contributor.authorIl Kim, Tae-
dc.contributor.authorCheon, Jae Hee-
dc.contributor.authorPark, Jihye-
dc.date.accessioned2026-03-23T06:20:54Z-
dc.date.available2026-03-23T06:20:54Z-
dc.date.created2026-03-23-
dc.date.issued2026-03-
dc.identifier.issn1976-2283-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/211427-
dc.description.abstractBackground/Aims: Intestinal Beh & ccedil;et&apos;s disease (BD) is a rare, chronic intestinal vascular disorder often refractory to conventional therapy. We aimed to assess the effectiveness and tolerability of anti-tumor necrosis factor alpha (anti-TNF-alpha) therapy in patients with moderate to severe refractory intestinal BD. Methods: Clinical remission, clinical response, and biological response rates at 4, 12, and 24 months, as well as the adverse effects of anti-TNF-alpha therapy were investigated at the Inflammatory Bowel Disease Center of Severance Hospital, Seoul, Korea. We also examined the relapse rates and predictive factors for disease relapse. Results: Of the 119 patients, 15 (12.6%) were bio-exposed, 68 (57.1%) received concomitant immunomodulators, and 56 (47.1%) received concomitant corticosteroids at anti-TNF-alpha treatment induction. At 4, 12, and 24 months, clinical remission rates were 23.5%, 40.3%, and 42.0%; clinical response rates were 84.0%, 62.2%, and 62.2%; and biological response rates were 61.3%, 68.9%, and 58.8%, respectively. Sixty-three patients (52.9%) relapsed, with a mean relapse time of 2.8 years. Higher initial C-reactive protein levels (hazards ratio [HR], 1.013; 95% confidence interval [CI], 1.008 to 1.018; p<0.001), history of previous intestinal surgery (HR, 4.282; 95% CI, 2.379 to 7.709; p<0.001), concomitant immunomodulator use (HR, 0.455; 95% CI, 0.267 to 0.775; p=0.004), and clinical response at 4 months (HR, 0.353; 95% CI, 0.181 to 0.687; p=0.002) were independent factors associated with the disease relapse. No mortality was observed during the study period; 26 (21.8%) and three patients (2.5%) experienced mild infection and infusion reactions, respectively. Conclusions: Anti-TNF-alpha therapy could be an effective and tolerable option for refractory intestinal BD. (Gut Liver, Published online November27, 2025)-
dc.languageEnglish-
dc.publisherEditorial Office of Gut and Liver-
dc.relation.isPartOfGUT AND LIVER-
dc.relation.isPartOfGUT AND LIVER-
dc.subject.MESHAdrenal Cortex Hormones / therapeutic use-
dc.subject.MESHAdult-
dc.subject.MESHBehcet Syndrome* / drug therapy-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHInfliximab / adverse effects-
dc.subject.MESHInfliximab / therapeutic use-
dc.subject.MESHIntestinal Diseases* / drug therapy-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRecurrence-
dc.subject.MESHRemission Induction-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHTumor Necrosis Factor-alpha* / antagonists & inhibitors-
dc.subject.MESHYoung Adult-
dc.titleEffectiveness and Tolerability of Anti-Tumor Necrosis Factor Alpha Therapy in Refractory Intestinal Behçet&apos;s Disease: A Large Single-Center Study-
dc.typeArticle-
dc.contributor.googleauthorChang, Ji Young-
dc.contributor.googleauthorKim, Jiwoo-
dc.contributor.googleauthorPark, Soo Jung-
dc.contributor.googleauthorPark, Jae Jun-
dc.contributor.googleauthorIl Kim, Tae-
dc.contributor.googleauthorCheon, Jae Hee-
dc.contributor.googleauthorPark, Jihye-
dc.identifier.doi10.5009/gnl250346-
dc.relation.journalcodeJ00954-
dc.identifier.eissn2005-1212-
dc.identifier.pmid41306097-
dc.subject.keywordBehcet disease-
dc.subject.keywordTumor necrosis factor inhibitors-
dc.subject.keywordRecurrence-
dc.contributor.affiliatedAuthorKim, Jiwoo-
dc.contributor.affiliatedAuthorPark, Soo Jung-
dc.contributor.affiliatedAuthorPark, Jae Jun-
dc.contributor.affiliatedAuthorIl Kim, Tae-
dc.contributor.affiliatedAuthorCheon, Jae Hee-
dc.contributor.affiliatedAuthorPark, Jihye-
dc.identifier.wosid001707717800001-
dc.citation.volume20-
dc.citation.number2-
dc.identifier.bibliographicCitationGUT AND LIVER, Vol.20(2), 2026-03-
dc.identifier.rimsid92155-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorBehcet disease-
dc.subject.keywordAuthorTumor necrosis factor inhibitors-
dc.subject.keywordAuthorRecurrence-
dc.subject.keywordPlusINFLAMMATORY-BOWEL-DISEASE-
dc.subject.keywordPlusBEHCETS-DISEASE-
dc.subject.keywordPlusRISK-FACTORS-
dc.subject.keywordPlusCONSENSUS STATEMENTS-
dc.subject.keywordPlusCOMBINATION THERAPY-
dc.subject.keywordPlusOUTCOMES-
dc.subject.keywordPlusINFLIXIMAB-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusEFFICACY-
dc.subject.keywordPlusANTIBODIES-
dc.type.docTypeArticle; Early Access-
dc.identifier.kciidART003315205-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.