Table 4.

Responses in evaluable patients (n = 43)

Lymphoma subtypeResponsesORR/ CR
B-NHL (n = 8) 
DLBCL (n = 6) CR (2), PR (2), SD (1), PD (1) 67%/33% 
Other B-cell (n = 2PD (2)  
T/NK-NHL (n = 15) 
Extranodal NK/T-cell lymphoma CR (1), PR (4), PD (3) 63%/13% 
PTCL, NOS CR (1), PR (1), PD (1) 67%/50% 
Angioimmunoblastic T-cell lymphoma CR (2), SD (1)  
Cutaneous T-cell lymphoma PD (1)  
Immunodeficiency-associated LPD (n = 10) 
PTLD CR (1), PD (2) 50%/33% 
Other (SLE, CVID, PI) CR (1), PR (1), PD (1)  
HIV-associated lymphoma (PBL, DLBCL [2], HL) PD (4)  
Hodgkin lymphoma (n = 10) PR (1), SD (5), PD (4) 10%/0% 
Total (n = 43 evaluable patients) CR (8), PR (9), SD (7), PD (19) 40%/19% 
Lymphoma subtypeResponsesORR/ CR
B-NHL (n = 8) 
DLBCL (n = 6) CR (2), PR (2), SD (1), PD (1) 67%/33% 
Other B-cell (n = 2PD (2)  
T/NK-NHL (n = 15) 
Extranodal NK/T-cell lymphoma CR (1), PR (4), PD (3) 63%/13% 
PTCL, NOS CR (1), PR (1), PD (1) 67%/50% 
Angioimmunoblastic T-cell lymphoma CR (2), SD (1)  
Cutaneous T-cell lymphoma PD (1)  
Immunodeficiency-associated LPD (n = 10) 
PTLD CR (1), PD (2) 50%/33% 
Other (SLE, CVID, PI) CR (1), PR (1), PD (1)  
HIV-associated lymphoma (PBL, DLBCL [2], HL) PD (4)  
Hodgkin lymphoma (n = 10) PR (1), SD (5), PD (4) 10%/0% 
Total (n = 43 evaluable patients) CR (8), PR (9), SD (7), PD (19) 40%/19% 

CVID, common variable immune deficiency; HL, Hodgkin lymphoma; LPD, lymphoproliferative disorder; NHL, non-Hodgkin lymphoma; PBL, plasmablastic lymphoma; PD, progressive disease; PI, primary immunodeficiency; SD, stable disease; SLE, systemic lupus erythematosus.

CD30+ B-cell lymphoma and B-LPD.

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