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Table 1 Baseline demographics and disease characteristics

From: fSCIG 10% in pediatric primary immunodeficiency diseases: a European post-authorization safety study

 

fSCIG 10%

new starters

(n = 23)

fSCIG 10%

pretreated

(n = 19)

Overall

(N = 42)

Age, years

 Mean (SD)

10.3 (3.8)

11.7 (4.3)

11.0 (4.1)

 Median (range)

11.0 (3–17)

12.0 (3–17)

11.5 (3–17)

Age group, years, n (%)

 2 to < 6 years

3 (13.0)

3 (15.8)

6 (14.3)

 6 to < 12 years

11 (47.8)

4 (21.1)

15 (35.7)

 12 to < 18 years

9 (39.1)

12 (63.2)

21 (50.0)

Male sex, n (%)

18 (78.3)

16 (84.2)

34 (81.0)

Ethnicity, n (%)

 Not Hispanic or Latino

23 (100)

19 (100)

42 (100)

Race, n (%)

 White

22 (95.7)

19 (100)

41 (97.6)

BMI, kg/m2

 Mean (SD)

19.0 (4.3)

20.4 (5.1)

19.7 (4.6)

 Median (range)

18.3 (12.3–30.3)

18.8 (13.5–32.7)

18.6 (12.3–32.7)

PIDs diagnosis, n (%)

 Agammaglobulinemia – AR

1 (4.3)

1 (5.3)

2 (4.8)

 Congenital agamma – XLA

8 (34.8)

8 (42.1)

16 (38.1)

 Common variable immunodeficiency

11 (47.8)

7 (36.8)

18 (42.9)

 Severe combined immune deficiency

0

1 (5.3)

1 (2.4)

 Activated phosphokinase 3 delta receptor syndrome§

0

1 (5.3)

1 (2.4)

 Hypogammaglobulinemia§

1 (4.3)

0

1 (2.4)

 NEMO immune deficiency§

2 (8.7)

0

2 (4.8)

 PI3K-delta syndrome§

0

1 (5.3)

1 (2.4)

  1. Age at baseline (last non-missing value before initial dose of fSCIG 10%)
  2. Race for one patient could not be collected as per local regulations
  3. §These diagnosis terms were provided by the reporting clinician when listing “Other” PIDs diagnoses
  4. AR, autosomal recessive; BMI, body mass index; fSCIG, hyaluronidase-facilitated subcutaneous immunoglobulin; NEMO, nuclear factor kappa B essential modulator; PI3K, phosphoinositide 3-kinase; PIDs, primary immunodeficiency diseases; SD, standard deviation; XLA, X-linked agammaglobulinemia