Real-world evaluation of effectiveness, persistence, and usage patterns of tofacitinib in treatment of rheumatoid arthritis in Australia

被引:25
作者
Bird, Paul [1 ,2 ]
Littlejohn, Geoffrey [1 ,3 ]
Butcher, Belinda [2 ,4 ]
Smith, Tegan [1 ]
Pereira, Candida da Fonseca [5 ]
Witcombe, David [5 ]
Griffiths, Hedley [1 ,6 ]
机构
[1] Opal Rheumatol Ltd, Sydney, NSW, Australia
[2] Univ New South Wales, Kensington, NSW, Australia
[3] Monash Univ, Clayton, Vic, Australia
[4] WriteSource Med Pty Ltd, Lane Cove, NSW, Australia
[5] Pfizer Australia, Sydney, NSW, Australia
[6] Barwon Rheumatol Serv, Geelong, Vic, Australia
关键词
Medication persistence; Real-world; Rheumatoid arthritis; Targeted synthetic disease-modifying antirheumatic drug; TNF-inhibitors; Tofacitinib; METHOTREXATE; MONOTHERAPY; OUTCOMES; COMBINATION; CP-690,550; SAFETY;
D O I
10.1007/s10067-020-05021-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction The aim of this study was to describe the real-world evidence for effectiveness, treatment persistence, and treatment patterns among patients in the community with rheumatoid arthritis treated with the JAK inhibitor tofacitinib. Methods This was a retrospective, non-interventional cohort study that extracted data for new users of tofacitinib or biologic disease-modifying antirheumatic drugs (bDMARDs) from the Australian Optimizing Patient outcomes in Australian RheumatoLogy (OPAL) dataset between March 2015 and September 2018. Patients were propensity score matched at a 1:2 tofacitinib to bDMARD ratio based on age, sex, and selected baseline treatment combinations. Treatment effectiveness was evaluated using disease status measures. Treatment persistence was calculated and the percentage of patients receiving monotherapy or combination therapy at treatment initiation was evaluated. Results Data from 2810 patients were extracted and 1950 patients were included in the matched population (1300 bDMARD initiators and 650 tofacitinib initiators). Patients were predominantly aged 55 to 74 years (57.8%) and female (81.2%). After 18 months of treatment, 52.4% and 57.8% of patients had achieved disease activity score (DAS) remission in the bDMARD and tofacitinib groups, respectively. The median treatment persistence for tofacitinib was similar to that for bDMARDs: 34.2 months (95% CI 32.2 to not reached) and 33.8 months (95% CI 28.8 to 40.4), respectively. In the overall population, more patients were prescribed tofacitinib as monotherapy (43.4%) compared with bDMARD monotherapy (33.4%). Conclusions Tofacitinib demonstrated treatment effectiveness and persistence similar to bDMARDs. Overall, there was a trend for more use of tofacitinib as monotherapy than bDMARDs.
引用
收藏
页码:2545 / 2551
页数:7
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