A systematic review and meta-analysis of infection risk with small molecule JAK inhibitors in rheumatoid arthritis

被引:208
作者
Bechman, Katie [1 ]
Subesinghe, Sujith [1 ]
Norton, Sam [2 ]
Atzeni, Fabiola [3 ]
Galli, Massimo [4 ,5 ]
Cope, Andrew P. [1 ]
Winthrop, Kevin L. [6 ]
Galloway, James B. [1 ]
机构
[1] Kings Coll London, Ctr Rheumat Dis, London, England
[2] Kings Coll London, Inst Psychiat, Psychol Dept, London, England
[3] Univ Messina, Clin & Expt Med, Rheumatol Unit, Messina, Italy
[4] Univ Milan, Luigi Sacco Dept Biomed & Clin Sci, Milan, Italy
[5] Luigi Sacco Hosp, ASST Fatebenefratelli Sacco, Div Infect Dis 3, Milan, Italy
[6] Oregon Hlth & Sci Univ, Div Infect Dis, Portland, OR 97201 USA
基金
英国医学研究理事会;
关键词
rheumatoid arthritis; systematic review; meta-analysis; immunosuppressants; viruses; MODIFYING ANTIRHEUMATIC DRUGS; VARICELLA-ZOSTER-VIRUS; INADEQUATE RESPONSE; TOFACITINIB CP-690,550; PHASE IIB; OPPORTUNISTIC INFECTIONS; HERPES-ZOSTER; BACKGROUND METHOTREXATE; INFLAMMATORY DISEASES; TREATED PATIENTS;
D O I
10.1093/rheumatology/kez087
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To evaluate the risk of serious infection (SI) and herpes zoster (HZ) in rheumatoid arthritis patients receiving JAK inhibitors. Methods. We conducted a systematic literature review and meta-analysis of phase II and III randomized controlled trials of tofacitinib (5 mg bid), baricitinib (4 mg od) and upadacitinib (15 mg od). Patient-exposure years were calculated. A per-protocol analysis was applied, incorporating follow-up time from patients randomized to placebo who cross into the treatment arm. Pooled incidence rates per 100 person-years of SI and HZ were calculated. Incidence rate ratios (IRRs) of drug vs placebo were compared using a meta-synthesis approach. Results. Twenty-one studies were included in the meta-analysis; 11 tofacitinib (5888 patients), six baricitinib (3520 patients) and four upadacitinib studies (1736 patients). For SI, the incidence rates were 1.97 (95% CI: 1.41, 2.68), 3.16 (95% CI: 2.07, 4.63) and 3.02 (95% CI: 0.98, 7.04), respectively. The IRRs comparing treatment arm to placebo were statistically non-significant: 1.22 (95% CI: 0.60, 2.45), 0.80 (95% CI: 0.46, 1.38) and 1.14 (95% CI: 0.24, 5.43), respectively. For HZ, the incidence rates were 2.51 (95% CI: 1.87, 3.30), 3.16 (95% CI: 2.07, 4.63) and 2.41 (95% CI: 0.66, 6.18), respectively. The IRR of HZ comparing baricitinib with placebo was 2.86 (95% CI: 1.26, 6.50). Non-significant IRRs were seen with tofacitinib and upadacitinib: 1.38 (95% CI: 0.66, 2.88) and 0.78 (95% CI: 0.19, 3.22), respectively. Indicator opportunistic infections excluding HZ were too rare to provide meaningful incidence rates. Conclusion. The absolute SI rates were low. However across the JAK inhibitors, the incidence of HZ is higher than expected for the population (3.23 per 100 patient-years). While the risk was numerically greatest with baricitinib, indirect comparisons between the drugs did not demonstrate any significant difference in risk.
引用
收藏
页码:1755 / 1766
页数:12
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