Table 1.

Baseline characteristics of 13 patients with WM treated with daratumumab

Characteristicn (%) or median (range)
Age at WM diagnosis, y 60 (42-77) 
Age at daratumumab initiation, y 69 (53-81) 
Time from WM to daratumumab, y 5.8 (2.3-27.4) 
Male sex 10 (77) 
Serum immunoglobulin M level, mg/dL 2031 (920-4566) 
Hemoglobin level, g/dL 12.4 (7.6-15) 
Platelet count, ×103/μL 176 (79-335) 
Serum β-2-microglobulin level, mg/L 3.9 (1.8-15.6) 
Bone marrow involvement, % 30 (5-80) 
Lymphadenopathy ≥1.5 cm 7 (54) 
Splenomegaly ≥15 cm 3 (23) 
MYD88 L265P mutation 11/12 (92) 
CXCR4 mutations 4/10 (40) 
Prior lines of therapy 3 (1-9) 
Prior anti-CD20 therapy 13 (100) 
Prior chemotherapy 10 (77) 
Prior proteasome inhibitors 7 (54) 
Prior BTK inhibitors 4 (31) 
Refractory to previous line of therapy 4 (31) 
IPSSWM  
 Low risk 2 (15) 
 Intermediate risk 8 (62) 
 High risk 3 (23) 
Characteristicn (%) or median (range)
Age at WM diagnosis, y 60 (42-77) 
Age at daratumumab initiation, y 69 (53-81) 
Time from WM to daratumumab, y 5.8 (2.3-27.4) 
Male sex 10 (77) 
Serum immunoglobulin M level, mg/dL 2031 (920-4566) 
Hemoglobin level, g/dL 12.4 (7.6-15) 
Platelet count, ×103/μL 176 (79-335) 
Serum β-2-microglobulin level, mg/L 3.9 (1.8-15.6) 
Bone marrow involvement, % 30 (5-80) 
Lymphadenopathy ≥1.5 cm 7 (54) 
Splenomegaly ≥15 cm 3 (23) 
MYD88 L265P mutation 11/12 (92) 
CXCR4 mutations 4/10 (40) 
Prior lines of therapy 3 (1-9) 
Prior anti-CD20 therapy 13 (100) 
Prior chemotherapy 10 (77) 
Prior proteasome inhibitors 7 (54) 
Prior BTK inhibitors 4 (31) 
Refractory to previous line of therapy 4 (31) 
IPSSWM  
 Low risk 2 (15) 
 Intermediate risk 8 (62) 
 High risk 3 (23) 

IPSSWM, International Prognostic Scoring System for WM.

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