SAT0204 Predictors for SLE flares: Baseline disease activity and demographic characteristics from the bliss trials’ combined placebo groups

Background Predicting which SLE patients are at increased risk for clinically meaningful flares may be useful in making management decisions. Objectives To identify demographic and disease-related predictors for flares. Methods Baseline demographic and SLE-related disease activity characteristics we...

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Veröffentlicht in:Annals of the rheumatic diseases 2013-06, Vol.71 (Suppl 3), p.540-541
Hauptverfasser: van Vollenhoven, R.F., Petri, M., Levy, R.A., Navarra, S., Buyon, J., Zhong, Z.J., Freimuth, W., Cervera, R.
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Sprache:eng
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Zusammenfassung:Background Predicting which SLE patients are at increased risk for clinically meaningful flares may be useful in making management decisions. Objectives To identify demographic and disease-related predictors for flares. Methods Baseline demographic and SLE-related disease activity characteristics were evaluated for their ability to predict new SLE flares by wk 24 in the combined dataset of 562 patients receiving placebo + standard therapy from the belimumab BLISS-52 (NCT00424476) and BLISS-76 (NCT00410384) phase 3 trials. Flare (moderate-severe) was defined according to the modified SLE Flare Index (SFI) or as the development of 1 new BILAG A or 2 new B organ domain scores. Baseline variables included race, age, gender, BMI, SELENA-SLEDAI (SS; mean score, range, and 24 items with ≥30/group), PGA, BILAG A-E scores, ACR diagnostic criteria, SLICC damage index, SLE duration, and concurrent medications. A ≥10% absolute difference (% flare - % no flare) or ≥50% increase ([% flare - % no flare]/% no flare) was considered clinically meaningful. Results By wk 24, 142 patients (25.3%) receiving placebo had a flare by BILAG and 72 (12.8%) by SFI. By both flare indices, SS ≥12, serologic markers, and moderate-severe disease activity involving renal, hematologic, and vasculitic domains were predictors of flare, as was prednisone use (table). Immunosuppressives, antimalarials, and other concomitant medications did not predict flare. Table 1. Predictors for Flare Characteristic% BILAG A/2B Flare% SFI Severe Flare WithWithoutWithWithout (n=142)(n=420)(n=72)(n=490) SS ≥1242.3#24.348.6#25.9 SS proteinuria21.8+11.427.8#12.0 SS vasculitis10.6*5.213.9*5.5 SS low complement73.2+56.977.8+58.6 SS DNA binding76.1*64.883.3+65.3 BILAG renal (A,B,C)53.6#33.561.1+35.3 BILAG vasculitic (A,B)13.47.919.5#7.7 BILAG hematologic (A,B)25.3+12.427.8+13.9 Any prednisone91.5+85.294.4*85.7 Nominal p values for pairwise comparison (likelihood ratio test). #p
ISSN:0003-4967
1468-2060
DOI:10.1136/annrheumdis-2012-eular.3151