THU0104 Limited Safety Signals, but No Advantage of Cobra-Light over Cobra Combination Therapy 4 Years after Initiation of The Cobra-Light Trial in Early Rheumatoid Arthritis

BackgroundCOBRA and COBRA-light combination therapy are equally effective and safe treatments for early rheumatoid arthritis (RA) after 26 and 52 weeks [1,2], but long-term safety of COBRA-light therapy is unknown.ObjectivesTo investigate survival and comorbidities of initial COBRA and COBRA-light combination therapy after a 4 year follow-up period. A detailed analysis of long-term efficacy will be presented separately.MethodsIn the COBRA-light trial, 164 patients with recent-onset RA were randomized to either COBRA (prednisolone 60 mg/day, tapered to 7.5 mg/day in 6 weeks; MTX 7.5 mg/wk and sulfasalazine 2 g/day; n=81) or COBRA-light therapy (prednisolone 30 mg/day, tapered to 7.5 mg/day in 8 weeks and MTX escalated to 25 mg/wk in 8 weeks; n=83). Between 26 and 52 weeks; treatment intensification of MTX and addition of etanercept was protocollized (treat-to-target). After 52 weeks, treatment was continued without protocol. Four year after trial initiation, all patients who had initiated therapy (n=162) were invited to participate in the COBRA-light extension study. All patients were interviewed and clinical records were protocollized examined for new comorbidities developed during the follow-up period.ResultsA total of 149 out of 162 original trial patients participated in the extension study (77 COBRA and 72 COBRA-light). During the follow-up period, 5 five patients had died: 2 COBRA (both cancer) and 3 COBRA-light (1x dementia; 2x unknown); 6 were not able or willing to participate, and 2 were in drug-free remission and out of care. After the 52 weeks trial period, 43% COBRA vs. 42% COBRA-light patients used prednisolone for ≥90 days, 34% vs. 44% switched to other DMARDs, and 39% vs. 28% used biologicals during the follow-up period. After mean 4 years follow-up, 118 patients (79% in each treatment group) had developed new comorbidities. Cardiovascular events, hypertension, hypercholesterolemia and diabetes mellitus were equally prevalent in both treatment groups (Table 1), notably angina pectoris and heart failure were not seen. Bone quality tended lower in the COBRA-light group, as evidenced by prevalence of osteoporosis on DXA (1% COBRA vs. 6% COBRA-light, p=0.20); clinical fractures (8% vs. 18%, p=0.06), and especially vertebral and rib fractures (0% vs. 6%, p=0.05). Seven patients developed cancer during follow-up: 2 COBRA (both lung cancer, both deceased during follow-up), and 5 COBRA-light (3x lung cancer, 1x basal cell carcinoma and 1x meningioma