Table 1.

Patient characteristics

CharacteristicResult, N = 57*
Age at ibrutinib initiation, median (range), y 67.7 (46.9-84.1) 
Male/female, n/n, (ratio) 39/18 (2.2) 
Prognostic factors, n/N (%)  
 11q deletion 18/40 (45) 
 17p deletion 20/47 (43) 
 Unmutated IGHV 34/38 (89) 
Previous lines, median (range) 2 (0-5) 
Previous lines, n (%)  
 FCR or BR 46 (81) 
 Alemtuzumab plus or minus dexamethasone 9 (16) 
 Chlorambucil plus or minus anti-CD20 14 (25) 
 Other 25 (44) 
Best response on ibrutinib therapy, investigator reported, n/N (%)  
 PR 48/55 (87) 
 PRl 7/55 (13) 
Transient dose interruption >7 d, n/N (%) 20/55 (37) 
Dose reduction, n/N (%) 23/55 (42) 
CharacteristicResult, N = 57*
Age at ibrutinib initiation, median (range), y 67.7 (46.9-84.1) 
Male/female, n/n, (ratio) 39/18 (2.2) 
Prognostic factors, n/N (%)  
 11q deletion 18/40 (45) 
 17p deletion 20/47 (43) 
 Unmutated IGHV 34/38 (89) 
Previous lines, median (range) 2 (0-5) 
Previous lines, n (%)  
 FCR or BR 46 (81) 
 Alemtuzumab plus or minus dexamethasone 9 (16) 
 Chlorambucil plus or minus anti-CD20 14 (25) 
 Other 25 (44) 
Best response on ibrutinib therapy, investigator reported, n/N (%)  
 PR 48/55 (87) 
 PRl 7/55 (13) 
Transient dose interruption >7 d, n/N (%) 20/55 (37) 
Dose reduction, n/N (%) 23/55 (42) 

BR, bendamustine plus rituximab; FCR, fludarabine plus cyclophosphamide plus rituximab; IGHV, immunoglobulin heavy chain variable gene; PR, partial response; PRl, partial response with lymphocytosis.

*

Except where otherwise stated.

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