Table 1.
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) |
The population used for this analysis includes all patients in the intent-to-treat set who received ≥1 dose of idelalisib.
Includes all patients treated during this study.
Age (years) = (date of first dose of study medication – date of birth + 1)/365.25.
BMI (kg/m2) = weight/height2.
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.