CONFERENCE UPDATE: EULAR 2026
Continuous treat-to-target ULT superior to discontinuation for gout remission: GO TEST FINALE
Current EULAR and American College of Rheumatology (ACR) guidelines recommend lifelong urate-lowering therapy (ULT) using a treat-to-target (T2T) strategy for maintaining gout remission.1 However, evidence comparing continued T2T ULT with ULT discontinuation in gout remission remains unclear.1 At the EULAR 2026 Congress, Professor Iris Rose Peeters from Sint Maartenskliniek, Netherlands, presented the 2-year results of the pragmatic, open-label, randomized GO-TEST FINALE trial, demonstrating that continued T2T ULT was superior to ULT discontinuation for maintaining gout remission.1
The multicenter trial enrolled patients with a clinical diagnosis of gout or who fulfilled the 2015 ACR/EULAR gout classification criteria, who had been receiving ULT and remained in remission for ≥12 months, defined by no flares or clinical tophi, serum urate ≤0.36mmol/L, gout pain score <2, and gout disease activity score <2.1 Key exclusions included clinically visible tophaceous gout, contraindications to standard gout therapies, regular use of gout medications for symptom prevention or treatment, or recent major cardiovascular disease.1
Patients were randomized 1:1 to either continued T2T ULT targeting serum urate < 0.36 mmol/L or an attempt at ULT discontinuation.1 In the discontinuation group, ULT was restarted if patients developed a flare lasting >7 days, >1 flare, or tophi.1 The primary endpoint was modified gout remission during Months 18-24, defined by no flares or clinical tophi, gout pain score <2, and gout disease activity score <2.1 Key secondary outcomes included flare-free survival, ULT and anti-inflammatory medication use, and adverse events.1
A total of 310 patients were randomized, with 309 included in the intention-to-treat analysis (155 in the ULT T2T continuation group and 154 in the discontinuation group).1 The study population was predominantly male, with a median age of 68 years in the continuation group and 67 years in the discontinuation group.1 Baseline characteristics were generally comparable, although hypertension and previous cerebrovascular or transient ischemic events were more frequent in the continuation group.1 Approximately 85% of patients fulfilled the ACR/EULAR gout classification criteria, and allopurinol was the most commonly used ULT.1
The primary endpoint significantly favored continued T2T ULT, with 79% of patients in the continuation group remaining in remission vs. 63% in the discontinuation group (risk difference=16%; 95% CI: 6-26; p=0.0015).1 Using simplified remission criteria, remission rates were 98.6% versus 86.4%, respectively (risk difference=12.2%; 95% CI: 6.3-18.1; p<0.001).1 Flare-free survival was also significantly higher with continued ULT (p<0.001).1
ULT discontinuation led to more frequent therapy restarts vs. T2T ULT (23% vs. 1.3%), with a median time to restart of 392 days.1 Anti-inflammatory medication use was also lower with continued ULT (18% vs. 36%; 95% CI: -27 to -8; p<0.001).1
Five deaths occurred during the study, with three in the continuation group and two in the discontinuation group, while rates of major non-fatal cardiovascular events remained similar between groups.1 Notably, kidney function declined significantly less over 24 months with continued T2T ULT, with a baseline-adjusted mean difference in estimated glomerular filtration rate of -1.84mL/min/1.73m² (95% CI: -3.52 to -0.15; p=0.033).1
In conclusion, the GO-TEST FINALE trial demonstrated that continued T2T ULT was superior to ULT discontinuation for maintaining gout remission over 2 years.1 Continued ULT was associated with fewer flares, lower use of anti-inflammatory medication, and a smaller decline in kidney function, supporting continued T2T management in patients with sustained gout remission.1