Efficacy, drug sustainability, and safety of ustekinumab treatment in Crohn's disease patients over three years.

Dorottya Angyal, Akos Ilias, Hajnal Szekely, Tamas G Toth, Zsolt Dubravcsik, Alexandra Farkas, Patricia Sarlos, Aron Vincze, Mark Juhasz, Petra A Golovics, Tamas Szamosi, Eszter Schafer, Fruzsina Balogh, Laszlo J Barkai, Tamas Molnar, Lorant Gonczi, Bernadett Farkas, Klaudia Farkas, Arpad Patai, Peter L Lakatos, Pal Miheller

Journal: Scientific reports 2024;14(1):14909

PMID: 38942890

Abstract

Long-term data on ustekinumab in real-life Crohn's disease patients are still missing, though randomized controlled trials demonstrated it as a favorable therapeutic option. We aimed to evaluate ustekinumab's clinical efficacy, drug sustainability, and safety in a prospective, nationwide, multicenter Crohn's disease patient cohort with a three-year follow-up. Crohn's disease patients on ustekinumab treatment were consecutively enrolled from 9 Hungarian Inflammatory Bowel Disease centers between January 2019 and May 2020. Patient and disease characteristics, treatment history, clinical disease activity (Harvey Bradshaw Index (HBI)), biomarkers, and endoscopic activity (Simple Endoscopic Score for Crohn's Disease (SES-CD)) were collected for three-years' time. A total of 148 patients were included with an overall 48.9% of complex behavior of the Crohn's disease and 97.2% of previous anti-TNF exposure. The pre-induction remission rates were 12.2% (HBI), and 5.1% (SES-CD). Clinical remission rates (HBI) were 52.2%, 55.6%, and 50.9%, whereas criteria of an endoscopic remission were fulfilled in 14.3%, 27.5%, and 35.3% of the subjects at the end of the first, second, and third year, respectively. Dose intensification was high with 84.0% of the patients on an 8-weekly and 29.9% on a 4-weekly regimen at the end of year 3. Drug sustainability was 76.9% during the follow-up period with no serious adverse events observed. Ustekinumab in the long-term is an effective, sustainable, and safe therapeutic option for Crohn's disease patients with severe disease phenotype and high previous anti-TNF biological failure, requiring frequent dose intensifications.

© 2024. The Author(s).

Address: Department of Internal Medicine and Oncology, Semmelweis University, Koranyi Sandor Utca 2A, 1083, Budapest, Hungary. [email protected].; Department of Internal Medicine and Oncology, Semmelweis University, Koranyi Sandor Utca 2A, 1083, Budapest, Hungary.; Department of Medicine, University of Szeged, Szeged, Hungary.; Department of Gastroenterology, Medical Centre, Hungarian Defence Forces, Budapest, Hungary.; Department of Medicine, St. Margit Hospital, Budapest, Hungary.; Department of Medicine and Gastroenterology, Markusovszky Hospital, Szombathely, Hungary.; First Department of Medicine, Medical School, University of Pecs, Pecs, Hungary.; Department of Gastroenterology, Bács-Kiskun County Hospital, Kecskemet, Hungary.; Department of Gastroenterology, St. Janos Hospital, Budapest, Hungary.; Department of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.; Department of Internal Medicine and Oncology, Semmelweis University, Koranyi Sandor Utca 2A, 1083, Budapest, Hungary.; Montreal General Hospital, McGill University Health Center, Montreal, Canada.
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