AI Article Synopsis

  • The study aimed to assess the effectiveness and safety of JAK inhibitors and S1P receptor modulators for treating chronic antibiotic-refractory pouchitis (CARP), as there is limited data on this.
  • Data from 15 patients were analyzed, revealing that after 3 months of treatment with JAK inhibitors, 53.3% had a clinical response and 40% achieved clinical remission, with some patients showing improvements after 12 months.
  • No side effects were reported, suggesting that these small molecules could be a promising option for CARP patients who haven’t responded to other biologic therapies, warranting further research.

Article Abstract

Background And Aims: Data regarding the effectiveness and safety of Janus kinase [JAK] inhibitors and sphingosine-1-phosphate [S1P] receptor modulators in antibiotic refractory chronic pouchitis [CARP] are lacking.

Methods: This ECCO-CONFER project retrospectively collected data for JAK inhibitor or S1P receptor modulator treatments for CARP with at least 3 months of follow-up. The outcomes included corticosteroid- and antibiotic-free clinical response and remission at 3 and 12 months, and trends in modified pouchitis disease activity index [mPDAI], endoscopic PDAI, C-reactive protein, and calprotectin.

Results: Seventeen treatments in 15 patients were evaluated. Previous pouchitis treatments included infliximab [5/15], adalimumab [4/15], vedolizumab [9/15], and ustekinumab [5/15]. Pooling data on JAK inhibitors [eight tofacitinib, one filgotinib, and six upadacitinib] after 3 months [T3], steroid- and antibiotic-free clinical response was achieved in 53.3% [8/15], and steroid- and antibiotic-free clinical remission was achieved in 40% [6/15]. Of the patients with at least 12 months of follow-up, steroid- and antibiotic-free clinical response was achieved in 50% [3/6] and remission in one patient [16.7%], endoscopic response in 50% [3/6], and endoscopic remission in 50% [3/6]. Of the two ozanimod treatments at T3, steroid- and antibiotic-free clinical response was achieved in one patient, without remission; both discontinued ozanimod before T12. No side effects were reported.

Conclusions: Small molecules may represent a suitable option for CARP refractory to multiple biologics, deserving further investigation.

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Source
http://dx.doi.org/10.1093/ecco-jcc/jjad194DOI Listing

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