Canakinumab for acute gouty arthritis in patients with limited treatment options: results from two randomised, multicentre, active-controlled, double-blind trials and their initial extensions

被引:244
作者
Schlesinger, Naomi [1 ]
Alten, Rieke E. [2 ]
Bardin, Thomas [3 ,4 ]
Schumacher, H. Ralph [5 ,6 ]
Bloch, Mark [10 ]
Gimona, Alberto [7 ,8 ]
Krammer, Gerhard [7 ,8 ]
Murphy, Valda [7 ,8 ]
Richard, Dominik [7 ,8 ]
So, Alexander K. [9 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Med, Div Rheumatol, New Brunswick, NJ 08901 USA
[2] Charite, Dept Internal Med, Schlosspk Klin, D-13353 Berlin, Germany
[3] Univ Paris 07, Paris, France
[4] Hop Lariboisiere, Serv Rhumatol, F-75475 Paris, France
[5] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[6] Univ Penn, VA Med Ctr, Philadelphia, PA 19104 USA
[7] Novartis Pharma AG, Dept Integrated Hosp Care Franchise Sci, Basel, Switzerland
[8] Novartis Pharma AG, Dept Integrated Informat Sci, Basel, Switzerland
[9] Univ Lausanne Hosp, Dept Rheumatol, Lausanne, Switzerland
[10] Holdsworth House Med Practice, Sydney, NSW, Australia
关键词
QUALITY-OF-LIFE; SERUM URIC-ACID; ACUTE FLARES; PHASE-II; MANAGEMENT; INDOMETHACIN; DIAGNOSIS; EFFICACY; HEALTH; URATE;
D O I
10.1136/annrheumdis-2011-200908
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Gouty arthritis patients for whom non-steroidal anti-inflammatory drugs and colchicine are inappropriate have limited treatment options. Canakinumab, an anti-interleukin-1 beta monoclonal antibody, may be an option for such patients. The authors assessed the efficacy/safety of one dose of canakinumab 150 mg (n = 230) or triamcinolone acetonide (TA) 40 mg (n = 226) at baseline and upon a new are in frequently flaring patients contraindicated for, intolerant of, or unresponsive to non-steroidal anti-inflammatory drugs and/or colchicine. Core study co-primary endpoints were pain intensity 72 h postdose (0-100 mm visual analogue scale and time to first new flare. Methods Two 12-week randomised, multicentre, active-controlled, double-blind, parallel-group core studies with double-blind 12-week extensions (response in acute flare and in prevention of episodes of re-flare in gout (beta-RELIEVED and beta-RELIEVED-II)). Results 82.6% patients had comorbidities. Mean 72-h visual analogue scale pain score was lower with canakinumab (25.0 mm vs 35.7 mm; difference, - 10.7 mm; 95% CI -15.4 to -6.0; p < 0.0001), with significantly less physician-assessed tenderness and swelling (ORs = 2.16 and 2.74; both p <= 0.01) versus TA. Canakinumab significantly delayed time to first new flare, reduced the risk of new flares by 62% versus TA (HR: 0.38; 95% CI 0.26 to 0.57) in the core studies and by 56% (HR: 0.44; 95% CI 0.32 to 0.60; both p <= 0.0001) over the entire 24-week period, and decreased median C-reactive protein levels (p <= 0.0001 at 72 h and 7 days). Over the 24-week period, adverse events were reported in 66.2% (canakinumab) and 52.8% (TA) and serious adverse events were reported in 8.0% (canakinumab) and 3.5% (TA) of patients. Adverse events reported more frequently with canakinumab included infections, low neutrophil count and low platelet count. Conclusion Canakinumab provided significant pain and inflammation relief and reduced the risk of new flares in these patients with acute gouty arthritis.
引用
收藏
页码:1839 / 1848
页数:10
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