PMID- 28094760 OWN - NLM STAT- MEDLINE DCOM- 20170613 LR - 20170613 IS - 0392-856X (Print) IS - 0392-856X (Linking) VI - 35 IP - 2 DP - 2017 Mar-Apr TI - Treat-to-target biologic therapy in patients with rheumatoid arthritis is more efficacious and safe compared to delayed initiation of biologics: a real-world study. PG - 192-200 AB - OBJECTIVES: Rheumatoid arthritis (RA) is a chronic, devastating disease. Treat-to-target strategy (T2T) more than the usual care, reduces disease activity by using aggressively all therapeutic options. The aim of the study was to evaluate our hypothesis that T2T strategy using biologic disease-modifying anti-rheumatic drugs (bDMARDs), when needed, is also safer than the usual care characterised by delayed initiation of bDMARDs. METHODS: Disease activity was regularly measured by DAS-28 until the end of treatment with the first bDMARD. All adverse events (AEs) and their severity were recorded. Cox proportional-hazards models were performed examining the association of treatment groups, with the risk of first AE. RESULTS: There were 113 patients in T2T and 250 patients in usual care group. The likelihood (adjusted hazard ratio, HR) of achieving remission or LDA was 71% higher in the T2T group than in the usual care group, as it has been already shown by others. The novel finding of our work was that AEs, including cancers, were less frequent in the T2T group with the corresponding HRs being less than 0.50 for serious AEs, infections and serious infections (significant or marginally non-significant results). There were 15 new cancer cases in usual care and 1 in T2T group (IR 1.99 vs. 0.4, p=0.027). CONCLUSIONS: Treat-to-target treatment with bDMARDs offers a safer, rapid and better long-term outcome to patients with RA. FAU - Lampropoulos, Christos E AU - Lampropoulos CE AD - Department of Pathophysiology, Medical School, National and Kapodistrian University of Athens, Greece. FAU - Orfanos, Philippos AU - Orfanos P AD - Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Greece. FAU - Manoussakis, Menelaos N AU - Manoussakis MN AD - Department of Pathophysiology, and Academic Joint Rheumatology Programme, Medical School, National and Kapodistrian University of Athens, Greece. FAU - Tzioufas, Athanasios G AU - Tzioufas AG AD - Department of Pathophysiology, and Academic Joint Rheumatology Programme, Medical School, National and Kapodistrian University of Athens, Greece. FAU - Moutsopoulos, Haralampos M AU - Moutsopoulos HM AD - Department of Pathophysiology, Medical School, National and Kapodistrian University of Athens, Greece. FAU - Vlachoyiannopoulos, Panayiotis G AU - Vlachoyiannopoulos PG AD - Department of Pathophysiology, and Academic Joint Rheumatology Programme, Medical School, National and Kapodistrian University of Athens, Greece. pvlah@med.uoa.gr. LA - eng PT - Comparative Study PT - Journal Article PT - Observational Study DEP - 20170116 PL - Italy TA - Clin Exp Rheumatol JT - Clinical and experimental rheumatology JID - 8308521 RN - 0 (Antirheumatic Agents) RN - 0 (Biological Products) SB - IM MH - Adult MH - Aged MH - Antirheumatic Agents/*administration & dosage/adverse effects MH - Arthritis, Rheumatoid/diagnosis/*drug therapy MH - Biological Products/*administration & dosage/adverse effects MH - Chi-Square Distribution MH - Drug Administration Schedule MH - Female MH - Humans MH - Kaplan-Meier Estimate MH - Male MH - Middle Aged MH - Proportional Hazards Models MH - Remission Induction MH - Retrospective Studies MH - Risk Factors MH - Severity of Illness Index MH - Time Factors MH - *Time-to-Treatment MH - Treatment Outcome EDAT- 2017/01/18 06:00 MHDA- 2017/06/14 06:00 CRDT- 2017/01/18 06:00 PHST- 2016/01/11 00:00 [received] PHST- 2016/05/02 00:00 [accepted] PHST- 2017/01/18 06:00 [pubmed] PHST- 2017/06/14 06:00 [medline] PHST- 2017/01/18 06:00 [entrez] AID - 10302 [pii] PST - ppublish SO - Clin Exp Rheumatol. 2017 Mar-Apr;35(2):192-200. Epub 2017 Jan 16.