Table 1.

Characteristics of patients with past HBV infection treated with ibrutinib (N = 21)

CharacteristicNo. of patients
Male sex 15 (71) 
Age, median (range), y 66 (50-83) 
Hematologic malignancy  
 CLL 15 (71) 
 Mantle cell lymphoma 4 (19) 
 Waldenstrom macroglobulinemia 2 (10) 
Duration of ibrutinib (mo), median (range) 9.5 (1-49) 
Anti-CD20 therapy* in previous 2 y 10 (48) 
Allo-HCT 5 (24) 
 Before ibrutinib 2 (10) 
 After ibrutinib 3 (14) 
Baseline HBV surface antibody >10 IU/L 17 (89) 
 Quantitative HBsAb, median (range), IU/L 260 (<5, >1000) 
HBV prophylaxis 1 (5) 
CharacteristicNo. of patients
Male sex 15 (71) 
Age, median (range), y 66 (50-83) 
Hematologic malignancy  
 CLL 15 (71) 
 Mantle cell lymphoma 4 (19) 
 Waldenstrom macroglobulinemia 2 (10) 
Duration of ibrutinib (mo), median (range) 9.5 (1-49) 
Anti-CD20 therapy* in previous 2 y 10 (48) 
Allo-HCT 5 (24) 
 Before ibrutinib 2 (10) 
 After ibrutinib 3 (14) 
Baseline HBV surface antibody >10 IU/L 17 (89) 
 Quantitative HBsAb, median (range), IU/L 260 (<5, >1000) 
HBV prophylaxis 1 (5) 

Data are presented as n (%) of patients unless indicated otherwise.

*

Anti-CD20 therapy given within 2 years before ibrutinib started included rituximab, ofatumumab, or obinutuzumab.

Includes information from 19 patients; baseline surface antibody before ibrutinib was not checked in 2 of 21 patients.

One patient was on HBV prophylaxis with entecavir that was started during a course of rituximab <1 year before ibrutinib was started. Entecavir continued during the entire ibrutinib course for this patient.

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