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. 2023 Aug 17;7(20):6055–6065. doi: 10.1182/bloodadvances.2023010840

Table 1.

Baseline patient demographic and disease characteristics

Characteristic Patients (n = 40)
Age, median (range), y 65 (39-79)
 18–65 y, n (%) 21 (52.5)
 >65 y, n (%) 19 (47.5)
Male, n (%) 22 (55.0)
ECOG PS, n (%)
 0 16 (40.0)
 1 22 (55.0)
 2 2 (5.0)
Ann Arbor stage at study entry, n (%)
 I to II 6 (15.0)
 III to IV 34 (85.0)
IPI score at study entry, n (%)
 2 19 (47.5)
 3 15 (37.5)
 4 6 (15.0)
Cell of origin by local laboratory, n (%)
 Germinal center B cell 17 (42.5)
 Nongerminal center B cell 21 (52.5)
 Unknown 2 (5.0)
Additional characterization by local laboratory, n (%)
 Rearrangements of MYC, BCL2, and/or BCL6 3 (7.5)
 Double expressor (MYC and BCL2 overexpression without translocation) 6 (15.0)
 None of the above 28 (70.0)
 Not determined/available 3 (7.5)

ECOG PS, Eastern Cooperative Oncology Group performance status; GEP, gene expression profiling; IHC, immunohistochemistry.

Thirteen patients assigned based on IHC and 4 assigned based on GEP.

Seventeen patients assigned based on IHC and 4 patients based on GEP (3 had activated B cell, and 1 was unclassified).

Includes 1 patient whose double expressor status was not confirmed until after the clinical cutoff date.