Table 1.

Selected baseline characteristics

CharacteristicParticipants (N = 32)
Age at WM diagnosis, median (range), y 58 (38-72) 
Age at venetoclax initiation, median (range), y 66 (39-80) 
Male sex, n (%) 18 (56) 
Serum IgM level, median (range), mg/dL 3512 (642-7970) 
Hemoglobin level, median (range), g/dL 10.6 (6.4-13.5) 
Platelet count, median (range), ×103/μL 216 (60-445) 
Serum β2-microglobulin level, median (range), mg/L 3.6 (1.9-9.8) 
Low IPSSWM score, n (%) 12 (38) 
Intermediate IPSSWM score, n (%) 8 (25) 
High IPSSWM score, n (%) 12 (38) 
Bone marrow involvement, median (range), % 35 (4-90) 
Adenopathy ≥1.5 cm, n (%) 9 (28) 
Splenomegaly ≥15 cm, n (%) 8 (25) 
MYD88 L265P mutation, n (%) 32 (100) 
CXCR4 mutation, n (%) 17 (53) 
No. of previous therapies, median (range) 2 (1-10) 
Previous anti-CD20 therapy, n (%) 28 (88) 
Previous BTK inhibitor, n (%) 16 (50) 
CharacteristicParticipants (N = 32)
Age at WM diagnosis, median (range), y 58 (38-72) 
Age at venetoclax initiation, median (range), y 66 (39-80) 
Male sex, n (%) 18 (56) 
Serum IgM level, median (range), mg/dL 3512 (642-7970) 
Hemoglobin level, median (range), g/dL 10.6 (6.4-13.5) 
Platelet count, median (range), ×103/μL 216 (60-445) 
Serum β2-microglobulin level, median (range), mg/L 3.6 (1.9-9.8) 
Low IPSSWM score, n (%) 12 (38) 
Intermediate IPSSWM score, n (%) 8 (25) 
High IPSSWM score, n (%) 12 (38) 
Bone marrow involvement, median (range), % 35 (4-90) 
Adenopathy ≥1.5 cm, n (%) 9 (28) 
Splenomegaly ≥15 cm, n (%) 8 (25) 
MYD88 L265P mutation, n (%) 32 (100) 
CXCR4 mutation, n (%) 17 (53) 
No. of previous therapies, median (range) 2 (1-10) 
Previous anti-CD20 therapy, n (%) 28 (88) 
Previous BTK inhibitor, n (%) 16 (50) 

IgM, immunoglobulin M; IPSSWM, International Prognostic Scoring for WM.

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