Tofacitinib for the Treatment of Ulcerative Colitis: An Integrated Summary of up to 7.8 Years of Safety Data from the Global Clinical Programme

Author:

Sandborn William J1,D’Haens Geert R2,Sands Bruce E3,Panaccione Remo4,Ng Siew C5,Lawendy Nervin6,Kulisek Nicole6,Modesto Irene7,Guo Xiang6,Mundayat Rajiv7,Su Chinyu6,Vranic Ivana8,Panés Julian9

Affiliation:

1. Division of Gastroenterology, University of California San Diego , La Jolla, CA , USA

2. Department of Gastroenterology, Amsterdam University Medical Centres , Amsterdam , The Netherlands

3. Dr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai , New York, NY , USA

4. Division of Gastroenterology and Hepatology, Department of Medicine, University of Calgary , Calgary, AB , Canada

5. Institute of Digestive Disease, Department of Medicine and Therapeutics, LKS Institute of Health Science, Chinese University of Hong Kong , Hong Kong

6. Pfizer Inc , Collegeville, PA , USA

7. Pfizer Inc , New York, NY , USA

8. Pfizer Ltd , Tadworth, Surrey , UK

9. Department of Gastroenterology, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd , Barcelona , Spain

Abstract

Abstract Background and Aims Tofacitinib is an oral small molecule Janus kinase [JAK] inhibitor for the treatment of ulcerative colitis. We report an integrated summary of tofacitinib safety [exposure: ≤7.8 years] from the global clinical programme. Methods Patients receiving tofacitinib 5 or 10 mg twice daily [BID] from completed phase [P]2/3 placebo-controlled studies, an open-label, long-term extension study [final data cut-off: August 24, 2020], and interim analysis of a P3b/4 study (interim data cut-off: February 20, 2020; Overall plus P3b/4 [2020] Cohort) were included. Proportions with adverse events [AEs] and serious AEs, and incidence rates [IRs; unique patients with events/100 patient-years] for deaths and AEs of special interest [AESI] were evaluated. Opportunistic infections, malignancies, major adverse cardiovascular events [MACE] and gastrointestinal perforations were adjudicated. Results In total, 1157 patients received one or more dose of tofacitinib (mean duration: 946.9 days); 955/1157 [83%] received a predominant dose of 10 mg BID; 412/1157 [35.6%] received tofacitinib for >4 years; 992/1157 [85.7%] had AEs, 244/1157 [21.1%] had serious AEs and 134/1157 (11.6%) discontinued use due to AEs. IRs [95% confidence intervals] for all tofacitinib doses were: deaths, 0.23 [0.09–0.46]; serious infections, 1.69 [1.26–2.21]; herpes zoster [non-serious and serious], 3.30 [2.67–4.04]; opportunistic infections, 1.03 [0.70–1.46]; malignancies (excluding non-melanoma skin cancer [NMSC]), 0.84 [0.55–1.24]; NMSC, 0.73 [0.45–1.10]; MACE, 0.29 [0.13–0.55]; deep vein thrombosis, 0.03 [0.00–0.18]; pulmonary embolism, 0.19 [0.07–0.42]; gastrointestinal perforations, 0.10 [0.02–0.28]. Conclusions AESI IRs were stable to 7.8 years and generally <2.0 in the Overall plus P3b/4 [2020] Cohort, with the exception of herpes zoster [a known risk of tofacitinib treatment]. ClinicalTrials.gov:NCT00787202;NCT01465763;NCT01458951;NCT01458574;NCT01470612;NCT03281304 JCC Topic/keyword selection: 3. Clinical trials

Funder

Pfizer

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

Reference46 articles.

1. Tofacitinib, an oral Janus kinase inhibitor, in active ulcerative colitis;Sandborn;N Engl J Med,2012

2. Tofacitinib as induction and maintenance therapy for ulcerative colitis;Sandborn;N Engl J Med,2017

3. Safety and efficacy of tofacitinib for treatment of ulcerative colitis: final analysis of OCTAVE Open, an open-label, long-term extension study with up to 7.0 years of treatment;Sandborn;Aliment Pharmacol Ther,2022

4. Outcomes of tofacitinib dose reduction in patients with ulcerative colitis in stable remission from the randomised RIVETING trial;Vermeire;J Crohns Colitis,2021

5. Malignancies in inflammatory bowel disease;Greuter;Digestion,2020

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