Emerging drugs for the treatment of inflammatory bowel disease. (2nd October 2022)

• Record Type: Journal Article
• Authors: Wong, Uni; Cross, Raymond K
• Is Part Of: Expert opinion on emerging drugs. Volume 27:Number 4(2022)
• Page Start: 369
• Page End: 377
• Publication Date: 2022-10-02
• Subjects: Crohn's disease -- ulcerative colitis -- anti-TNF -- anti-integrin -- anti-IL12/23 -- anti-IL23 -- S1P receptor modulator -- JAK inhibitor -- mRNA-124; Drugs -- Research -- Handbooks, manuals, etc; Drugs -- Design -- Periodicals; 615.1072
• DOI: 10.1080/14728214.2022.2147507
• Languages: English
• ISSNs: 1472-8214

Abstract

ABSTRACT: Introduction: Anti-tumor necrosis factor (TNF)-α have been the mainstay therapy for Crohn's (CD) and ulcerative colitis (UC) for decades. With growing need for highly effective therapy, various therapeutic targets have been introduced including anti-integrins, anti-interleukin (IL) 12/23, selective anti-IL23, Janus Kinase (JAK) inhibitors, sphingosine-1-phosphate (S1P) receptor modulators, and mRNA-124 splicing agent. Areas covered: The current state of available IBD therapies and those in development are reviewed, with recommendations made on positioning in clinical practice. Expert opinion: Selecting and sequencing IBD therapies remains a clinical challenge. Disease phenotype, severity of symptoms, patient comorbidities, and prior drug exposure should be considered when considering therapy options. Anti-TNF remains a time-tested option that is effective in both UC and CD. The perception that newer biologics have slower onset of action is probably overestimated and providers should reconsider need for concurrent corticosteroid. JAK-inhibitors provide rapid symptom improvement in patients with moderate-severe UC. Due to safety concerns, it is recommended as a second-line therapy for UC. The goal for IBD treatment should be personalized, have rapid onset of action, induce durable clinical and endoscopic remission, and have excellent safety.