OP35 Endoscopic and deep remission at 1 year prevents disease progression in early Crohn’s disease: long-term data from CALM

Clara Yzet(Centre Hospitalier Universitaire Amiens-Picardie), Ryan C. Ungaro(Icahn School of Medicine at Mount Sinai), Peter Bossuyt(Imelda Hospital), Filip Baert(AZ Delta), Thomas Vanasek(University Hospital Hradec Králové), Geert D’Haens(University of Amsterdam), V Joustra(Amsterdam University Medical Centers), Remo Panaccione(University of Calgary), Gottfried Novacek(Medical University of Vienna), Alessandro Armuzzi(Università Cattolica del Sacro Cuore), Oleksandr Golovchenko(Kyiv City Clinical Oncology Center), O Prymak(Kyiv City Clinical Oncology Center), Adrian Goldiș(Spitalul Clinic de Recuperare), Simon Travis(University of Oxford), Xavier Hébuterne(Hôpital l'Archet), Marc Ferrante, Gerhard Rogler(University Hospital of Zurich), Mathurin Fuméry(Centre Hospitalier Universitaire Amiens-Picardie), Silvio Danese(Humanitas University), Grażyna Rydzewska(Central Clinical Hospital), Benjamin Pariente(Hôpital Claude Huriez), Erik Hertervig(Skåne University Hospital), C Stanciu(Grigore T. Popa University of Medicine and Pharmacy), JC Grimaud, M-M Diculescu(Carol Davila University of Medicine and Pharmacy), Laurent Peyrin‐Biroulet(Centre Hospitalier Régional et Universitaire de Nancy), David Laharie(Hôpital Cardiologique du Haut-Lévêque), John Wright, Fernando Gomollón(Instituto de Investigación Sanitaria Aragón), И. В. Губонина(S. M. Kirov Military Medical Academy), Stefan Schreiber(Kiel University), Satoshi Motoya(Sapporo Kosei General Hospital), Per M. Hellström(Uppsala University Hospital), Jonas Halfvarson(Örebro University), J F Colombel(Icahn School of Medicine at Mount Sinai)
Journal of Crohn s and Colitis
January 25, 2019
Cited by 14

Abstract

We aimed to describe the long-term impact of achieving endoscopic and deep remission among participants in the effect of tight control management on CD (CALM) trial. We analysed medical records from patients with follow-up data since end of CALM. Patients were stratified by outcomes in CALM at 1 year: clinical remission (Crohn’s disease activity index, CDAI <150), endoscopic remission (Crohn’s disease endoscopic index of severity, CDEIS <4 with no deep ulcerations), and deep remission (CDAI <150, CDEIS <4 with no deep ulcerations, and no steroids for ≥8 weeks). The primary outcome was a composite of major adverse outcomes reflecting CD progression: new internal fistula/abscess, stricture, perianal fistula/abscess, CD hospitalisation, or CD surgery since end of CALM. Kaplan–Meier and Cox regression methods were used to compare composite rates between patients who achieved or did not achieve remission at 1 year. Adjusted hazard ratios (aHR) with 95% confidence intervals (CI) are reported, controlling for randomisation arm and baseline variables significant at p < 0.2 level. One hundred twenty-two patients with median age 29 years (IQR 22.5–37) and median disease duration 0.2 years (IQR 0.1–0.8) were included. Median follow-up time from end of CALM was 3.02 years (range 0.05–6.26 years). Fifty per cent were randomised to the tight control arm. There were no significant differences in baseline characteristics in patients with follow-up data and those lost to follow-up with the exception of a slightly higher CDEIS score in patients lost to follow-up (14.6 vs. 12.9, p = 0.04). Thirty-four patients (27.9%) had a major adverse outcome during follow-up. Patients in clinical remission at 1 year did not have significantly lower rates of the composite endpoint (log-rank p = 0.15). Patients in endoscopic and deep remission at the end of CALM were significantly less likely to have a major adverse event over time (Figures 1 and 2). After adjusting for age, disease duration, prior surgery, prior stricture, and randomisation arm, endoscopic remission (aHR 0.44, 95% CI 0.20–0.96, p = 0.038) and deep remission (aHR 0.25, 95% CI 0.09–0.72, p = 0.01) were significantly associated with lower risk of major adverse events. Early CD patients who achieve endoscopic or deep remission after 1 year of intensive treatment are less likely to have disease progression over a median of 3 years. Abstract OP035 – Figure 1. Kaplan–Meier estimates of CD disease progression based on endoscopic remission at 1 year Abstract OP035 – Figure 2. Kaplan–Meier estimates of CD disease progression based on deep remission at 1 year.


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