Table 1

Patient demographics and disease characteristics

Anifrolumab combined (n=96)Anifrolumab BR (n=45)Anifrolumab IR (n=51)Placebo (n=49)
Patient demographics
 Age, yearsMedian (range)34.5 (18, 67)34.0 (19, 67)35.0 (18, 65)32.0 (18, 58)
 SexFemale, n (%)82 (85.4)37 (82.2)45 (88.2)38 (77.6)
 WeightMean (SD), kg65.4 (15.0)62.7 (12.3)67.7 (16.8)65.6 (13.3)
 BMIMean (SD)25.1 (5.06)24.0 (3.77)26.0 (5.85)24.5 (3.93)
>28 kg/m2, n (%)23 (24.0)7 (15.6)16 (31.4)9 (18.4)
 Race, n (%)White42 (43.8)17 (37.8)25 (49.0)24 (49.0)
Black/African American6 (6.3)2 (4.4)4 (7.8)1 (2.0)
Asian18 (18.8)11 (24.4)7 (13.7)10 (20.4)
Native Hawaiian/Pacific Islander1 (1.0)1 (2.2)00
American Indian/Alaska Native4 (4.2)3 (6.7)1 (2.0)0
Other25 (26.0)11 (24.4)14 (27.5)14 (28.6)
Hispanic or Latino ethnicity, n (%)45 (46.9)22 (48.9)23 (45.1)20 (40.8)
 Geographic region, n (%)Asia Pacific18 (18.8)10 (22.2)8 (15.7)9 (18.4)
Europe26 (27.1)10 (22.2)16 (31.4)15 (30.6)
Latin America34 (35.4)14 (31.1)20 (39.2)16 (32.7)
North America18 (18.8)11 (24.4)7 (13.7)9 (18.4)
Baseline disease characteristics
 Time from initial LN diagnosis to randomisation, mean (range), months6.8
(0.4, 306.9)
3.4
(1.1, 212.7)
15.7
(0.4, 306.9)
37.0
(0.7, 328.3)
 Renal biopsy result at screening, n (%)Class III17 (17.7)7 (15.6)10 (19.6)6 (12.2)
Class III+V11 (11.5)7 (15.6)4 (7.8)5 (10.2)
Class IV53 (55.2)26 (57.8)27 (52.9)30 (61.2)
Class IV+V15 (15.6)5 (11.1)10 (19.6)8 (16.3)
 24-hour UPCR, mg/mgMean (SD)3.10 (2.18)3.36 (2.50)2.86 (1.85)3.71 (3.20)
>3.0, n (%)36 (37.5)19 (42.2)17 (33.3)23 (46.9)
 eGFR* mL/min/1.73 m2 Mean (SD)97.1 (44.77)100.2 (46.77)94.4 (43.22)87.3 (35.43)
≥60, n (%)73 (76.0)35 (77.8)38 (74.5)39 (79.6)
 SLEDAI-2K† scoreMean (SD)10.7 (4.83)10.4 (4.63)11.0 (5.04)11.3 (4.38)
≥10, n (%)51 (53.1)23 (51.1)28 (54.9)29 (59.2)
 Non-renal SLEDAI-2K† scoreMean (SD)4.7 (3.12)5.2 (3.44)4.2 (2.74)4.7 (2.30)
 IFNGS statusHigh, n (%)91 (94.8)44 (97.8)47 (92.2)46 (93.9)
 Serology, n (%)ANA positive‡90 (93.8)44 (97.8)46 (90.2)49 (100)
Anti-dsDNA positive§76 (79.2)37 (82.2)39 (76.5)39 (79.6)
Low C3¶57 (59.4)30 (66.7)27 (52.9)42 (85.7)
Low C4¶24 (25.0)10 (22.2)14 (27.5)20 (40.8)
Baseline treatments
 Oral glucocorticoids**Yes, n (%)94 (97.9)43 (95.6)51 (100)48 (98.0)
Dosage, mean (SD), mg/day22.6 (10.63)21.9 (10.4)23.2 (10.88)21.9 (11.20)
≥20 mg/day, n (%)67 (69.8)31 (68.9)36 (70.6)33 (67.3)
 MMF before randomisationYes, n (%)72 (75.0)36 (80.0)36 (70.6)33 (67.3)
Dosage, mean (SD), g/day1.81 (0.502)1.82 (0.551)1.79 (0.460)1.77 (0.469)
Concomitant ACEI/ARB treatment, n (%)63 (65.6)27 (60.0)36 (70.6)33 (67.3)
Antimalarials, n (%)57 (59.4)31 (68.9)26 (51.0)35 (71.4)
  • Baseline is defined as the last measurement prior to randomisation and dose administration on day 1.

  • *eGFR is calculated using the MDRD formula.

  • †The SLEDAI-2K is a 24-item weighted score of lupus activity that ranges from 0 to 105, with higher scores indicating greater disease activity.

  • ‡ANA positive was defined as a titre ≥1:40.

  • §Anti-dsDNA positive was defined as an anti-dsDNA level above the assay cut-off for positive.

  • ¶Low complement level at baseline was defined as a complement level below lower limit of normal.

  • **Baseline oral glucocorticoid dosage is defined as the maximum daily dose of prednisone or equivalent taken between day 1 and day 7, inclusive.

  • ACEI, ACE inhibitors; ANA, antinuclear antibodies; anti-dsDNA, anti-double-stranded DNA; ARB, angiotensin receptor blockers; BMI, body mass index; BR, basic regimen; C3, complement 3; C4, complement 4; eGFR, estimated glomerular filtration rate; IFNGS, interferon gene signature; IR, intensified regimen; LN, lupus nephritis; MDRD, modification of diet in renal disease; MMF, mycophenolate mofetil; SLEDAI-2K, Systemic Lupus Erythematosus Disease Activity Index 2000; UPCR, urine protein–creatinine ratio.