Comparative risk of reactivation of hepatitis B and C after treatment with biologics and targeted synthetic DMARDs in psoriasis and psoriatic arthritis: A 15-year multicenter cohort study
- PMID: 40972765
- DOI: 10.1016/j.jaad.2025.09.030
Comparative risk of reactivation of hepatitis B and C after treatment with biologics and targeted synthetic DMARDs in psoriasis and psoriatic arthritis: A 15-year multicenter cohort study
Abstract
Background: The relative risks of HBV reactivation (HBVr) and HCV reactivation (HCVr) associated with different immunosuppressant agents in psoriasis and psoriatic arthritis are unknown.
Objective: We assessed the comparative risks of HBVr and HCVr for patients treated with biologics and targeted synthetic disease-modifying antirheumatic drugs.
Methods: We screened 5,527 treatment episodes (TEs) with available HBV and HCV serology data from 3197 patients who received biologics or targeted synthetic disease-modifying antirheumatic drugs; 1525 eligible TEs (1343 HBV TEs; 182 HCV TEs) were included.
Results: HBVr and HCVr occurred in 143 (10.6%) and 18 (9.9%) of TEs during 2104.5 and 271.2 person-years of follow-up, respectively. The risks of HBVr and HCVr were highest for tumor necrosis factor-α inhibitors, followed by interleukin-12/23 inhibitor (IL-12/23i), IL-17i, and IL-23i. Analysis revealed drug class (tumor necrosis factor-α inhibitors), hepatitis B surface antigen-positivity, hepatitis B e-antigen-positivity, concomitant use of immunosuppressants, and absence of antiviral prophylaxis were significantly associated with HBVr; a higher baseline viral load and drug class (tumor necrosis factor-α inhibitors) were associated with HCVr.
Limitations: Observational design and nonrandom treatment allocation.
Conclusions: The differential risks of HBVr and HCVr should be considered when selecting targeted therapies in psoriasis and psoriatic arthritis, particularly for patients with risk factors for viral reactivation.
Keywords: biologics; hepatitis B; hepatitis C; immunosuppressant; psoriasis; reactivation; tsDMARDs.
Copyright © 2025 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflicts of interest All authors have completed the ICMJE uniform disclosure form available at www.icmje.org/coi_disclosure.pdf and declare the following: Drs Chiu and Hui received speaking fees and received honoraria for serving as an advisory board member from AbbVie, Novartis, Janssen-Cilag, Eli-Lilly, Kyowa Hakko Kirin Taiwan, GlaxoSmithKline, UCB, Boehringer Ingelheim, and Pfizer pharmaceuticals and conducted clinical trials for AbbVie, Eli-Lilly, Sanofi Pharmaceuticals, Janssen-Cilag Pharmaceuticals. Dr Tsai has served as a consultant for Abbvie, AnaptysBio, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Eli-Lilly, Galderma, GSK, Janssen-Cilag, Leo Pharma, Merck Sharp and Dohme, Novartis International, Pfizer, PharmaEssentia, Sanofi, Sun Pharma and UCB Pharma. Dr Hung has received speaking fees from AbbVie, Novartis, Janssen-Cilag Pharmaceutica, Kyowa Hakko Kirin Taiwan, Pfizer, and Sanofi Pharmaceuticals Corporation. Dr Wu has received speaking fees from AbbVie, Novartis Pharmaceuticals Corporation, Janssen-Cilag Pharmaceutica, Eli-Lilly, Kyowa Hakko Kirin Taiwan, Boehringer Ingelheim Taiwan, UCB Pharmaceuticals (Taiwan) Ltd, and Pfizer Limited and conducted clinical trials for AbbVie, Novartis Pharmaceuticals Corporation, Janssen-Cilag Pharmaceutica, UCB Pharmaceuticals (Taiwan) Ltd, Pfizer Limited, AMGen, and Sanofi. Dr Chiu has received speaking fees from AbbVie, Novartis Pharmaceuticals Corporation, Janssen-Cilag Pharmaceutica, and Pfizer Limited and received honoraria for serving as a consultant for AbbVie, Novartis Pharmaceuticals Corporation, and Janssen-Cilag Pharmaceutica. Dr Hsu have received speaking fees from AbbVie, Eli-Lilly, Janssen-Cilag Pharmaceutica, Kyowa Hakko Kirin Taiwan, Leo Pharma, Novartis Pharmaceuticals Corporation, and Sanofi. Dr Chen has received speaking fees from AbbVie, Novartis Pharmaceuticals Corporation, Janssen-Cilag Pharmaceutica, Eli-Lilly, Kyowa Hakko Kirin Taiwan, Pfizer Limited and Sanofi, and conducted clinical trials or received honoraria for serving as a consultant for Novartis Pharmaceuticals Corporation, Eli-Lilly and Sanofi. Dr Yang has served as a consultant for Abbvie, Boehringer Ingelheim, Eli-Lilly, GSK, Janssen, Novartis, Pfizer and Sanofi. Dr Huang has conducted clinical trials for serving as a principal investigator for Galderma, Eli-Lilly, Novartis Pharmaceuticals Corporation, and Janssen-Cilag Pharmaceutica; received honoraria for serving as an advisory board member for Pfizer Limited, AbbVie, and Celgene; and received speaking fees from AbbVie, Eli-Lilly, and Novartis Pharmaceuticals Corporation. Drs Chia Hsu, Wei, Lan, Lee, Mong Chiu, Chi, Tseng, and Lai have no conflicts of interest to declare.
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