Journal Watch

This retrospective observational study included 180 patients receiving risankizumab over 2.5 years across eight centers in Japan.Median age was 38.5 years, 69% were men, and median follow-up was 52 weeks.Seventy-seven percent of the cohort had received advanced therapies, 58% had received at least two agents, and 46% had previously received ustekinumab.Almost half had undergone intestinal resection.The primary clinical-effectiveness analysis included only 51 patients with baseline Crohn's Disease Activity Index (CDAI) ≥220.Corticosteroid-free clinical remission required CDAI <150 without systemic corticosteroids or budesonide for at least 4 weeks.Endoscopic response required a ≥50% reduction in the Simple Endoscopic Score for Crohn's Disease (SES-CD); remission required SES-CD ≤2.Analyses used available observations without imputing missing outcomes.Among patients with moderate-to-severe active disease, corticosteroid-free remission occurred in 31% at week 12 (15/48), 52% at week 28 (22/42), and 57% at week 52 (16/28).Corresponding clinical-remission rates were 40, 55, and 61%, while clinical-response rates were 71, 74, and 75%.Outcomes generally favored patients without previous advanced-therapy exposure.At week 12, corticosteroid-free remission was 60% in treatment-naïve patients vs 18% in treatmentexposed patients.Ustekinumab-naïve patients also had better early outcomes, although differences between ustekinumab subgroups were not statistically significant at week 52.Paired endoscopic assessments were available for 45 patients.Overall, 58% achieved endoscopic response and 29% achieved endoscopic remission.Remission was more frequent in advanced-therapy-naïve than exposed patients (56 vs 14%) and in ustekinumab-naïve than exposed patients (44 vs 6%).Segmentbased analyses showed particularly favorable colonic outcomes in treatment-naïve groups.Similar trends in terminal ileal disease did not reach statistical significance.Inflammatory biomarkers, including C-reactive protein and leucine-rich α2-glycoprotein, generally decreased.Perianal outcomes were exploratory: among 20 evaluable patients at week

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Publication Details

Journal
Annals of Pediatric Gastroenterology and Hepatology ISPGHAN
Published
2026-10-28
DOI
https://doi.org/10.5005/jp-journals-11009-0204
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

Journal Watch

Rimjhim Shrivastava
Annals of Pediatric Gastroenterology and Hepatology ISPGHAN
Inflammatory Bowel Disease
article

Journal Watch

Rimjhim Shrivastava
article en

Abstract

This retrospective observational study included 180 patients receiving risankizumab over 2.5 years across eight centers in Japan.Median age was 38.5 years, 69% were men, and median follow-up was 52 weeks.Seventy-seven percent of the cohort had received advanced therapies, 58% had received at least two agents, and 46% had previously received ustekinumab.Almost half had undergone intestinal resection.The primary clinical-effectiveness analysis included only 51 patients with baseline Crohn's Disease Activity Index (CDAI) ≥220.Corticosteroid-free clinical remission required CDAI <150 without systemic corticosteroids or budesonide for at least 4 weeks.Endoscopic response required a ≥50% reduction in the Simple Endoscopic Score for Crohn's Disease (SES-CD); remission required SES-CD ≤2.Analyses used available observations without imputing missing outcomes.Among patients with moderate-to-severe active disease, corticosteroid-free remission occurred in 31% at week 12 (15/48), 52% at week 28 (22/42), and 57% at week 52 (16/28).Corresponding clinical-remission rates were 40, 55, and 61%, while clinical-response rates were 71, 74, and 75%.Outcomes generally favored patients without previous advanced-therapy exposure.At week 12, corticosteroid-free remission was 60% in treatment-naïve patients vs 18% in treatmentexposed patients.Ustekinumab-naïve patients also had better early outcomes, although differences between ustekinumab subgroups were not statistically significant at week 52.Paired endoscopic assessments were available for 45 patients.Overall, 58% achieved endoscopic response and 29% achieved endoscopic remission.Remission was more frequent in advanced-therapy-naïve than exposed patients (56 vs 14%) and in ustekinumab-naïve than exposed patients (44 vs 6%).Segmentbased analyses showed particularly favorable colonic outcomes in treatment-naïve groups.Similar trends in terminal ileal disease did not reach statistical significance.Inflammatory biomarkers, including C-reactive protein and leucine-rich α2-glycoprotein, generally decreased.Perianal outcomes were exploratory: among 20 evaluable patients at week

Annals of Pediatric Gastroenterology and Hepatology ISPGHANVol. 7(3)
Openalex Percentile: Top 14%
Inflammatory Bowel Disease
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