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Risk for Herpes Zoster in Tofacitinib‐Treated Rheumatoid Arthritis Patients With and Without Concomitant Methotrexate and Glucocorticoids
Author(s) -
Curtis Jeffrey R.,
Xie Fenglong,
Yang Shuo,
Bernatsky Sasha,
Chen Lang,
Yun Huifeng,
Winthrop Kevin
Publication year - 2019
Publication title -
arthritis care and research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.032
H-Index - 163
eISSN - 2151-4658
pISSN - 2151-464X
DOI - 10.1002/acr.23769
Subject(s) - tofacitinib , medicine , rheumatoid arthritis , concomitant , methotrexate , hazard ratio , incidence (geometry) , confidence interval , physics , optics
Objective Increased incidence of herpes zoster ( HZ ) has been observed with JAK inhibitors such as tofacitinib. However, whether concomitant methotrexate ( MTX ) and/or glucocorticoids confer additional (additive or multiplicative) risk is unclear. We evaluated HZ risk in tofacitinib users with and without MTX and glucocorticoids. Methods Within MarketScan and Medicare data (2011–2016), we identified all patients with rheumatologist‐diagnosed rheumatoid arthritis initiating treatment with tofacitinib (index date); demographics and baseline covariates were evaluated in the year prior to the index date. HZ was ascertained using International Classification of Diseases, Ninth Revision or Tenth Revision codes with antiviral drug use (±7 days). Multivariable Cox regression was used to evaluate hazard ratios ( HR s) for HZ in tofacitinib users with and without current concomitant MTX and glucocorticoids, controlling for baseline covariates. Results We studied 8,030 new tofacitinib users (83.3% women). The mean ± SD age was 60.3 ± 12.6 years. HZ incidence in tofacitinib users was numerically lowest in the absence of glucocorticoids (3.4 per 100 patient‐years with MTX ; 3.7 per 100 patient‐years without MTX ). An approximately 2‐fold increased incidence of HZ was observed for tofacitinib users receiving either glucocorticoids alone (6.0 per 100 patient‐years) or both MTX plus glucocorticoids (6.5 per 100 patient‐years). The adjusted HR for HZ in tofacitinib users was unchanged ( HR 0.99 [95% confidence interval (95% CI ) 0.64–1.54]) when given only with MTX , but was increased ( HR 1.96 [95% CI 1.33–2.88]) for tofacitinib plus glucocorticoids. Older age and female sex were also risk factors, while prior vaccination was associated with a strong trend for lower risk. Conclusion In tofacitinib users, HZ occurred at a rate of approximately 4% per year and was further doubled with glucocorticoid exposure. Concomitant MTX did not confer additional risk. Zoster vaccination may decrease risk.