PMID- 28079510 OWN - NLM STAT- MEDLINE DCOM- 20170831 LR - 20181202 IS - 0392-856X (Print) IS - 0392-856X (Linking) VI - 35 IP - 4 DP - 2017 Jul-Aug TI - A comparison of discontinuation rates of tofacitinib and biologic disease-modifying anti-rheumatic drugs in rheumatoid arthritis: a systematic review and Bayesian network meta-analysis. PG - 689-699 AB - OBJECTIVES: The purpose of this study was to compare the discontinuation rates of tofacitinib and biologics (tumour necrosis factor inhibitors (TNFi), abatacept, rituximab, and tocilizumab) in rheumatoid arthritis (RA) patients considering inadequate responses (IRs) to previous treatment(s). METHODS: Randomised controlled trials of tofacitinib and biologics - reporting at least one total discontinuation, discontinuation due to lack of efficacy (LOE), and discontinuation due to adverse events (AEs) - were identified through systematic review. The analyses were conducted for patients with IRs to conventional synthetic disease-modifying anti-rheumatic drugs (cDMARDs) and for patients with biologics-IR, separately. Bayesian network meta-analysis was used to estimate rate ratio (RR) of a biologic relative to tofacitinib with 95% credible interval (CrI), and probability of RR being <1 (P[RR<1]). RESULTS: The analyses of 34 studies showed no significant differences in discontinuation rates between tofacitinib and biologics in the cDMARDs-IR group. In the biologics-IR group, however, TNFi (RR 0.17, 95% CrI 0.01-3.61, P[RR<1] 92.0%) and rituximab (RR 0.20, 95% CrI 0.01-2.91, P[RR<1] 92.3%) showed significantly lower total discontinuation rates than tofacitinib did. Despite the difference, discontinuation cases owing to LOE and AEs revealed that tofacitinib was comparable to the biologics. CONCLUSIONS: The comparability of discontinuation rate between tofacitinib and biologics was different based on previous treatments and discontinuation reasons: LOE, AEs, and total (due to other reasons). Therefore, those factors need to be considered to decide the optimal treatment strategy. FAU - Park, Sun-Kyeong AU - Park SK AD - School of Pharmacy, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea. FAU - Lee, Min-Young AU - Lee MY AD - School of Pharmacy, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea. FAU - Jang, Eun-Jin AU - Jang EJ AD - Department of Information Statistics, Andong National University, Gyeongsangbuk-do, South Korea. FAU - Kim, Hye-Lin AU - Kim HL AD - College of Pharmacy, Sahmyook University, Seoul, South Korea. FAU - Ha, Dong-Mun AU - Ha DM AD - School of Pharmacy, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea. FAU - Lee, Eui-Kyung AU - Lee EK AD - School of Pharmacy, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea. ekyung@skku.edu. LA - eng PT - Comparative Study PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20170105 PL - Italy TA - Clin Exp Rheumatol JT - Clinical and experimental rheumatology JID - 8308521 RN - 0 (Antirheumatic Agents) RN - 0 (Biological Products) RN - 0 (Piperidines) RN - 0 (Protein Kinase Inhibitors) RN - 0 (Pyrimidines) RN - 0 (Pyrroles) RN - 87LA6FU830 (tofacitinib) SB - IM MH - Antirheumatic Agents/*therapeutic use MH - Arthritis, Rheumatoid/*drug therapy MH - Bayes Theorem MH - Biological Products/*therapeutic use MH - *Deprescriptions MH - Humans MH - Network Meta-Analysis MH - Piperidines/*therapeutic use MH - Protein Kinase Inhibitors/*therapeutic use MH - Pyrimidines/*therapeutic use MH - Pyrroles/*therapeutic use EDAT- 2017/01/13 06:00 MHDA- 2017/09/01 06:00 CRDT- 2017/01/13 06:00 PHST- 2016/08/31 00:00 [received] PHST- 2016/11/21 00:00 [accepted] PHST- 2017/01/13 06:00 [pubmed] PHST- 2017/09/01 06:00 [medline] PHST- 2017/01/13 06:00 [entrez] AID - 11072 [pii] PST - ppublish SO - Clin Exp Rheumatol. 2017 Jul-Aug;35(4):689-699. Epub 2017 Jan 5.