Table 2.

Summary of patient best responses as assessed by an IEAC

PopulationNORR, n (%)CR, n (%)CRu, n (%)PR, n (%)SD, n (%)PD, n (%)
All patients 25 12 (48.0) 5 (20.0) 7 (28.0) 10 (40.0) 3 (12.0) 
ATL subtype        
Acute 16 10 (62.5) 5 (31.3) 5 (31.3) 4 (25.0) 2 (12.5) 
Lymphoma 1 (16.7) 1 (16.7) 5 (83.3) 
Unfavorable chronic 1 (33.3) 1 (33.3) 1 (33.3) 1 (33.3) 
Disease site        
Nodal or extranodal lesions 20 10 (50.0) 6 (30.0) 2 (10.0) 2 (10.0) 7 (35.0) 3 (15.0) 
Skin lesions  3 (42.9) 1 (14.3) Not evaluable 2 (28.6) 3 (42.9) 
Peripheral blood 8 (88.9) 2 (22.2) Not evaluable 6 (66.7) 1 (11.1) 
Disease status        
Relapsed 3 (37.5) 1 (12.5) 2 (25.0) 4 (50.0) 1 (12.5) 
Recurrent 4 (66.7) 1 (16.7) 3 (50.0) 2 (33.3) 
Refractory 11 5 (45.5) 3 (27.3) 2 (18.2) 4 (36.4) 2 (18.2) 
Prior mogamulizumab treatment        
Yes 24 11 (45.8) 4 (16.7) 7 (29.2) 10 (41.7) 3 (12.5) 
No 1 (100.0) 1 (100.0) 
Prior lenalidomide treatment        
Yes 4 (50.0) 4 (50.0) 3 (37.5) 1 (12.5) 
No 17 8 (47.1) 5 (29.4) 3 (17.6) 7 (41.2) 2 (11.8) 
PopulationNORR, n (%)CR, n (%)CRu, n (%)PR, n (%)SD, n (%)PD, n (%)
All patients 25 12 (48.0) 5 (20.0) 7 (28.0) 10 (40.0) 3 (12.0) 
ATL subtype        
Acute 16 10 (62.5) 5 (31.3) 5 (31.3) 4 (25.0) 2 (12.5) 
Lymphoma 1 (16.7) 1 (16.7) 5 (83.3) 
Unfavorable chronic 1 (33.3) 1 (33.3) 1 (33.3) 1 (33.3) 
Disease site        
Nodal or extranodal lesions 20 10 (50.0) 6 (30.0) 2 (10.0) 2 (10.0) 7 (35.0) 3 (15.0) 
Skin lesions  3 (42.9) 1 (14.3) Not evaluable 2 (28.6) 3 (42.9) 
Peripheral blood 8 (88.9) 2 (22.2) Not evaluable 6 (66.7) 1 (11.1) 
Disease status        
Relapsed 3 (37.5) 1 (12.5) 2 (25.0) 4 (50.0) 1 (12.5) 
Recurrent 4 (66.7) 1 (16.7) 3 (50.0) 2 (33.3) 
Refractory 11 5 (45.5) 3 (27.3) 2 (18.2) 4 (36.4) 2 (18.2) 
Prior mogamulizumab treatment        
Yes 24 11 (45.8) 4 (16.7) 7 (29.2) 10 (41.7) 3 (12.5) 
No 1 (100.0) 1 (100.0) 
Prior lenalidomide treatment        
Yes 4 (50.0) 4 (50.0) 3 (37.5) 1 (12.5) 
No 17 8 (47.1) 5 (29.4) 3 (17.6) 7 (41.2) 2 (11.8) 

RD: received ≥1 prior chemotherapy, achieved CR or CRu, and subsequently experienced disease progression. Recurrent disease: received ≥1 prior chemotherapy, achieved PR, and subsequently experienced disease progression. Refractory: received ≥1 prior chemotherapy and either achieved SD requiring a treatment switch or subsequently experienced PD.

One patient was not evaluated for skin lesions after baseline assessment.

Close Modal

or Create an Account

Close Modal
Close Modal