Table 1.

Clinicopathologic and treatment characteristics

CharacteristicAll patients (N = 19)
Age, median (range), y 69 (33-98) 
Sex, no. (%)  
 Female 6 (32) 
 Male 13 (68) 
International Prognostic Index score, no. (%)  
 <3 6 (32) 
 ≥3 13 (68) 
Histologic classification, no. (%)  
 DLBCL 14 (74) 
 HGBL 5 (26) 
Prior low-grade lymphoma, no. (%)  
 No 14 (74) 
 Yes 5 (26) 
Ki67, median (range), % 80 (50-95) 
COO by Hans algorithm, no. (%)  
 GCB 4 (21) 
 NGC 15 (79) 
Fluorescence in situ hybridization, no. (%)  
MYC rearrangement present 7/14 (50) 
BCL2 rearrangement present 3/12 (25) 
BCL6 rearrangement present 1/7 (14) 
 Double-hit lymphoma 
MYD88 L265P mutation present 1/6 (17) 
Front-line chemotherapy, no. (%)  
 R-CHOP 14 (74) 
 Intensive 5 (26) 
Second-line therapy, no. (%)  
 Curative-intent cytotoxic therapy 10 (53) 
 Other cytotoxic therapy 2 (10) 
 Ibrutinib 3 (16) 
 Other noncytotoxic therapy 4 (21) 
Prior ASCT, no. (%)  
 No 11 (58) 
 Yes 8 (42) 
Ibrutinib as line of therapy, no. (%)  
 Second 3 (16) 
 Third 8 (42) 
 Fourth 4 (21) 
 ≥Fifth 4 (21) 
Duration from start of prior therapy to start of ibrutinib, no. (%), mo  
 0-6 15 (79) 
 6-12 3 (16) 
 >12 1 (5) 
CharacteristicAll patients (N = 19)
Age, median (range), y 69 (33-98) 
Sex, no. (%)  
 Female 6 (32) 
 Male 13 (68) 
International Prognostic Index score, no. (%)  
 <3 6 (32) 
 ≥3 13 (68) 
Histologic classification, no. (%)  
 DLBCL 14 (74) 
 HGBL 5 (26) 
Prior low-grade lymphoma, no. (%)  
 No 14 (74) 
 Yes 5 (26) 
Ki67, median (range), % 80 (50-95) 
COO by Hans algorithm, no. (%)  
 GCB 4 (21) 
 NGC 15 (79) 
Fluorescence in situ hybridization, no. (%)  
MYC rearrangement present 7/14 (50) 
BCL2 rearrangement present 3/12 (25) 
BCL6 rearrangement present 1/7 (14) 
 Double-hit lymphoma 
MYD88 L265P mutation present 1/6 (17) 
Front-line chemotherapy, no. (%)  
 R-CHOP 14 (74) 
 Intensive 5 (26) 
Second-line therapy, no. (%)  
 Curative-intent cytotoxic therapy 10 (53) 
 Other cytotoxic therapy 2 (10) 
 Ibrutinib 3 (16) 
 Other noncytotoxic therapy 4 (21) 
Prior ASCT, no. (%)  
 No 11 (58) 
 Yes 8 (42) 
Ibrutinib as line of therapy, no. (%)  
 Second 3 (16) 
 Third 8 (42) 
 Fourth 4 (21) 
 ≥Fifth 4 (21) 
Duration from start of prior therapy to start of ibrutinib, no. (%), mo  
 0-6 15 (79) 
 6-12 3 (16) 
 >12 1 (5) 
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