Association Between Smoking Status and the Efficacy and Safety of Tofacitinib in Patients with Ulcerative Colitis

Author:

Rubin David T1,Torres Joana234ORCID,Regueiro Miguel5ORCID,Reinisch Walter6ORCID,Prideaux Lani7,Kotze Paulo G8,Tan Fiona H9ORCID,Gardiner Sean10ORCID,Mundayat Rajiv10,Cadatal Mary Jane11,Ng Siew C12

Affiliation:

1. Inflammatory Bowel Disease Center, University of Chicago Medicine , Chicago, IL , USA

2. Gastroenterology Division, Hospital Beatriz Ângelo , Loures , Portugal

3. Division of Gastroenterology, Hospital da Luz , Lisbon , Portugal

4. Faculdade de Medicina, Universidade de Lisboa , Lisbon , Portugal

5. Department of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic , Cleveland, OH , USA

6. Department of Internal Medicine III, Medical University of Vienna , Vienna , Austria

7. Department of Gastroenterology and Hepatology, Monash Medical Centre , Melbourne, Victoria , Australia

8. IBD Outpatient Clinics, Colorectal Surgery Unit, Catholic University of Paraná , Curitiba , Brazil

9. Pfizer Australia , Melbourne, Victoria , Australia

10. Pfizer Inc , New York, NY , USA

11. Pfizer Inc , Manila , Philippines

12. Department of Medicine and Therapeutics, Institute of Digestive Disease, LKS Institute of Health Science, Chinese University of Hong Kong , Sha Tin, Hong Kong , China

Abstract

Abstract Background Tofacitinib is an oral Janus kinase inhibitor for the treatment of ulcerative colitis (UC). This analysis assessed the impact of cigarette smoking on tofacitinib efficacy and safety in the UC clinical program. Methods Efficacy endpoints and adverse events (AEs) were evaluated by smoking status (ever smokers [current and ex-smokers] and never smokers) in the phase (P)2 induction study (baseline demographics and safety only), P3 studies (OCTAVE Induction 1&2, OCTAVE Sustain, OCTAVE Open), and P3/4b RIVETING study. Results This post hoc analysis included 1156 patients (ever smokers, n = 416 [36.0%; current smokers, n = 59 (5.1%); ex-smokers, n = 357 (30.9%)]; never smokers, n = 740 [64.0%]; median [range] treatment duration 654 [1–2712] and 615.5 [1–2850] days, respectively). Similar proportions of ever smokers and never smokers achieved efficacy endpoints. AEs were reported in 88.7% of ever smokers and 83.8% of never smokers. Overall, 60.6% of ever smokers had an infection (serious infections, 5.5%; herpes zoster [nonserious and serious], 10.8%; Clostridioides difficile infection, 12.0%; lower respiratory tract infection, 19.5%: corresponding values among never smokers were 53.1%, 3.9%, 6.8%, 8.5%, and 11.4%). Major adverse cardiovascular events were reported in 1.0% of ever smokers and 0.7% of never smokers and thromboembolism events (venous and arterial) in 1.0% of ever smokers and 0.9% never smokers. Deaths, malignancies (excluding non-melanoma skin cancer [NMSC]), and NMSC occurred infrequently in ever smokers (0.5%, 2.5%, and 3.7%, respectively) and never smokers (0.1%, 1.5%, and 1.0%, respectively). Colorectal cancer was reported in 0.6% of never smokers; no cases occurred in ever smokers. Conclusions Efficacy and safety of tofacitinib were generally similar in ever smokers and never smokers. Overall, serious AEs and, as expected, infections were more frequent in ever smokers versus never smokers. This may inform treatment selection and monitoring strategies. ClinicalTrials.gov NCT00787202;NCT01465763;NCT01458951;NCT01458574;NCT01470612;NCT03281304

Funder

Pfizer

Publisher

Oxford University Press (OUP)

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