@article {Mease1550, author = {Philip J Mease and Alice B Gottlieb and D{\'e}sir{\'e}e van der Heijde and Oliver FitzGerald and Alyssa Johnsen and Marleen Nys and Subhashis Banerjee and Dafna D Gladman}, title = {Efficacy and safety of abatacept, a T-cell modulator, in a randomised, double-blind, placebo-controlled, phase III study in psoriatic arthritis}, volume = {76}, number = {9}, pages = {1550--1558}, year = {2017}, doi = {10.1136/annrheumdis-2016-210724}, publisher = {BMJ Publishing Group Ltd}, abstract = {Objectives To assess the efficacy and safety of abatacept, a selective T-cell costimulation modulator, in a phase III study in psoriatic arthritis (PsA).Methods This study randomised patients (1:1) with active PsA (~60\% with prior exposure to a tumour necrosis factor inhibitor) to blinded weekly subcutaneous abatacept 125 mg (n=213) or placebo (n=211) for 24 weeks, followed by open-label subcutaneous abatacept. Patients without >=20\% improvement in joint counts at week 16 were switched to open-label abatacept. The primary end point was the proportion of patients with >=20\% improvement in the American College of Rheumatology (ACR20) criteria at week 24.Results Abatacept significantly increased ACR20 response versus placebo at week 24 (39.4\% vs 22.3\%; p\<0.001). Although abatacept numerically increased Health Assessment Questionnaire{\textendash}Disability Index response rates (reduction from baseline >=0.35) at week 24, this was not statistically significant (31.0\% vs 23.7\%; p=0.097). The benefits of abatacept were seen in ACR20 responses regardless of tumour necrosis factor inhibitor exposure and in other musculoskeletal manifestations, but significance could not be attributed due to ranking below Health Assessment Questionnaire{\textendash}Disability Index response in hierarchical testing. However, the benefit on psoriasis lesions was modest. Efficacy was maintained or improved up to week 52. Abatacept was well tolerated with no new safety signals.Conclusions Abatacept treatment of PsA in this phase III study achieved its primary end point, ACR20 response, showed beneficial trends overall in musculoskeletal manifestations and was well tolerated. There was only a modest impact on psoriasis lesions.Trial registration number ClinicalTrials.gov number, NCT01860976 (funded by Bristol-Myers Squibb).}, issn = {0003-4967}, URL = {https://ard.bmj.com/content/76/9/1550}, eprint = {https://ard.bmj.com/content/76/9/1550.full.pdf}, journal = {Annals of the Rheumatic Diseases} }