Skip to main content
. 2017 Jan 24;28(5):1057–1063. doi: 10.1093/annonc/mdx028

Table 1.

Demographics and baseline characteristicsa

Idelalisib
N = 25b
Male, n  (%) 11  (44)
Race, n  (%)
 White 19  (76)
 Black or African American 2  (8)
 Asian 1  (4)
 Other 3  (12)
Ethnicity, n (%)
 Hispanic or Latino 3  (12)
 Not Hispanic or Latino 22  (88)
Agec, years, median  (range) 42  (21–80)
BMId, kg/m2, mean  (SD) 25  (5.94)
ECOG performance status, n  (%)
 0 10  (40)
 1 10  (40)
 2 1  (4)
 Missing 4  (16)
Time since diagnosise, years, mean  (SD) 3.9  (4.26)
Prior therapies, median  (range) 5  (2–9)
Type of previous treatment, n  (%)
 BV 23  (92)
 ASCT 18  (72)
 Radiation therapy 11  (44)
Classical HL pathologic subtype, n  (%)
 Nodular sclerosis 23  (92)
 Lymphocyte rich 2  (8)
Disease stage at screening, n  (%)
 I–II 9  (36)
 III–IV 16  (64)
a

The population used for this analysis includes all patients in the intent-to-treat set who received ≥1 dose of idelalisib.

b

Includes all patients treated during this study.

c

Age  (years) = (date of first dose of study medication – date of birth + 1)/365.25.

d

BMI  (kg/m2) = weight/height2.

e

Time since diagnosis is calculated in months as  (date of randomization to the primary study – date of diagnosis)/30.4375.

ASCT, autologous stem cell transplant; BMI, body mass index; BV, brentuximab vedotin; ECOG, Eastern Cooperative Oncology Group; HL, Hodgkin lymphoma; SD, standard deviation.