DOP57 Monitoring response to anti-TNF therapy in ulcerative colitis patients by gastrointestinal ultrasound: sub-analysis from TRUST&UC
Abstract Background In ulcerative colitis GIUS (GastroIntestinal UltraSound) is discussed to be a reliable surrogate parameter for inflammatory activity next to faecal calprotectin (FC), and to some extend C-reactive protein (CRP). Treat to target (T2T) is an emerging concept of IBD management, whic...
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Published in | Journal of Crohn's and colitis Vol. 13; no. Supplement_1; pp. S063 - S064 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
US
Oxford University Press
25.01.2019
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Online Access | Get full text |
ISSN | 1873-9946 1876-4479 1876-4479 |
DOI | 10.1093/ecco-jcc/jjy222.091 |
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Summary: | Abstract
Background
In ulcerative colitis GIUS (GastroIntestinal UltraSound) is discussed to be a reliable surrogate parameter for inflammatory activity next to faecal calprotectin (FC), and to some extend C-reactive protein (CRP). Treat to target (T2T) is an emerging concept of IBD management, which might lead to superior outcomes with regard to mucosal healing, steroid-free remission, and hospitalisation as shown with anti-TNF therapies in previous studies.1 To ensure a stringent T2T approach, it is crucial to facilitate non-invasive, inexpensive, and reliable diagnostics to monitor disease activity. Recently, we published a multi-centre study evaluating the capability of GIUS to monitor therapy response in Crohn’s disease patients.2,3 Here we provide a first subgroup analysis of the TRUST&UC study (TRansabdominal UltraSonography of the bowel To monitor disease activity in subjects with ulcerative colitis) focussing on the monitoring of anti-TNF therapy response in ulcerative colitis patients.
Methods
In this sub-analysis of TRUST&UC, a prospective, observational multi-centre study, GIUS, clinical (Simple Clinical Colitis Activity Index, SCCAI) and laboratory parameters (CRP, FC) were assessed during anti-TNF therapy at week 0, 2, 6, and 12 in patients with active UC (SCCAI ≥ 5) and an increased bowel wall thickening (BWT) at baseline. Threshold for normal BWT was >4 mm for sigmoid colon and >3 mm for the descending colon.
Results
Within the study population, 29% (65/224) of patients received an anti-TNF therapy (adalimumab, infliximab, or golimumab) at least at one time during the study. Mean disease duration was 7.56 ± 8.39 years. A majority of TNF-treated patients had an increased BWT at baseline, a high clinical activity, represented by an SCCAI of 9.52 ± 2.62, and an increased FC level (n = 39, 1609 ± 1721.7 µg/g). The clinical activity changed significantly within 6 weeks for 61.5% (n = 40) of the patients (9.08 ± 2.27 vs. 4.23 ± 4.00, p < 0.001). Of the patients with anti-TNF therapy at baseline and Week 6 (n = 44) 47.7% (n = 21) experienced a normalisation and 34.1% (n = 15) a reduction of BWT at sigmoid colon or descending colon already within 6 weeks upon anti-TNF therapy. Patients with an ongoing vascularisation at Week 6 and 12 had a significantly higher SCCAI compared with patients with no colour Doppler signal (p < 0.001).
Conclusions
We demonstrated that anti-TNF treatment results in normalisation/reduction of BWT in a majority of UC patients as early as 6 weeks after start of anti-TNF therapy. Consequently, GIUS is useful in early monitoring of therapy response to anti-TNF therapy in UC patients enabling a non-invasive, easy, and repeatable means of tight control in daily practice.
References
1. Colombel J-F, Panaccione R, Bossuyt P, et al. Effect of tight control management on Crohn's disease (CALM): a multicentre, randomised, controlled phase 3 trial. Lancet 2017;390. doi:10.1016/S0140-6736(17)32641-7
2. Kucharzik T, Wittig BM, Helwig U, et al. Use of intestinal ultrasound to monitor Crohn's disease activity. Clin Gastroenterol Hepatol 2017;15:535–42.
3. Kucharzik T, Maaser C, Helwig U, et al. Monitoring response to adalimumab therapy in Crohn’s disease patients by bowel ultrasound: sub-analysis from TRUST. J Crohns Colitis 2018; Abtract P424. |
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ISSN: | 1873-9946 1876-4479 1876-4479 |
DOI: | 10.1093/ecco-jcc/jjy222.091 |