Safety of the JAK and TNF inhibitors in rheumatoid arthritis: real world data from the Hong Kong Biologics Registry

Author:

Mok Chi Chiu1ORCID,So Ho2,Yim Cheuk Wan3,To Chi Hung4,Lao Weng Nga5,Wong Stella Pui Yan6,Ng Hoi Yan7,Lee Jolly Man Yee8,Lee Patrick Man Leung9,Ying Shirley King Yee10,Leung Moon Ho11ORCID,Ho Carmen Tze Kwan12

Affiliation:

1. Department of Medicine, Tuen Mun Hospital , Hong Kong SAR, China

2. Department of Medicine, Prince of Wales Hospital , Hong Kong SAR, China

3. Department of Medicine, Tseung Kwan O Hospital , Hong Kong SAR, China

4. Department of Medicine, Pok Oi Hospital , Hong Kong SAR, China

5. Department of Medicine, Kwong Wah Hospital , Hong Kong SAR, China

6. Department of Medicine, Hong Kong Sanatorium and Hospital , Hong Kong SAR, China

7. Department of Medicine, Caritas Medical Center , Hong Kong SAR, China

8. Department of Medicine, Tai Po Hospital , Hong Kong SAR, China

9. Department of Medicine, Yan Chai Hospital , Hong Kong SAR, China

10. Department of Medicine, Princess Margaret Hospital , Hong Kong SAR, China

11. Department of Medicine, Queen Elizabeth Hospital , Hong Kong SAR, China

12. Department of Medicine, Queen Mary Hospital , Hong Kong SAR, China

Abstract

Abstract Objectives To compare the incidence of major adverse cardiovascular events (MACEs), cancer and infective complications in RA patients using Janus kinase (JAKis) and TNF (TNFis) inhibitors. Method A retrospective analysis of data from the Hong Kong Biologics Registry 2008–2021 was performed. RA patients who had ever used JAKis or TNFis were included. The incidence of MACEs, cancer and infections were compared between the two groups, with adjustment for confounding factors. Results A total of 2471 courses of JAKis (n = 551) and TNFis (n = 1920) were used in 1732 RA patients (83.7% women, age 53.8 [12.5] years; follow-up 6431 patient-years). JAKi users had significantly older age, more atherosclerotic risk factors and higher frequency of past malignancies. A total of 15 and 40 MACEs developed in the JAKi and TNFi users, respectively (incidence 1.34 vs 0.75 per 100 patient-years; P = 0.22). There was no significant difference in the incidence of cancers between the two groups (0.81 [JAKi] vs 0.85 [TNFi] per 100 patient-years; P = 0.25). The adjusted hazard ratios of MACE and cancer in the JAKi users were 1.36 (95% CI: 0.62, 2.96) (P = 0.44) and 0.87 (95% CI: 0.39, 1.95) (P = 0.74), respectively. Rates of infections were significantly higher in the JAKi than TNFi users (16.3 vs 9.9 per 100 patient-years; P = 0.02), particularly herpes zoster (3.49 vs 0.94 per 100 patient-years; P < 0.001). Conclusions In a real-life setting, there is no increase in MACEs or cancers in users of JAKis compared with TNFis. However, the incidence of non-serious infections, including herpes zoster, was increased in users of JAKis.

Funder

Hong Kong Society of Rheumatology

Pfizer

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference36 articles.

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