Table 2.

Response to induction therapy

Newly diagnosedRelapses*Oral ATRA FailureTotal
Group 1Group 2
Intent-to-treat patients       
 n = 32 n = 35 n = 20 n = 15 n = 2 n = 69 
No. remission (%) 20 (62%) 17 (49%) 14 (70%) 3 (20%) 1 (50%) 38 (57%) 
 Early death 12 20 
 Resistant 10 11  
Evaluable patients       
 n = 23 n = 31 n = 18 n = 13 n = 2 n = 56 
No. remission (%) 20 (87%) 17 (55%) 14 (71%) 3 (23%) 1 (50%) 38 (63%) 
 Early death 
 Resistant 
Newly diagnosedRelapses*Oral ATRA FailureTotal
Group 1Group 2
Intent-to-treat patients       
 n = 32 n = 35 n = 20 n = 15 n = 2 n = 69 
No. remission (%) 20 (62%) 17 (49%) 14 (70%) 3 (20%) 1 (50%) 38 (57%) 
 Early death 12 20 
 Resistant 10 11  
Evaluable patients       
 n = 23 n = 31 n = 18 n = 13 n = 2 n = 56 
No. remission (%) 20 (87%) 17 (55%) 14 (71%) 3 (23%) 1 (50%) 38 (63%) 
 Early death 
 Resistant 
*

Group 1: includes first-relapse patients who had not received oral all-trans retinoic acid (ATRA) for at least 1 year before relapse and 4 ATRA naive relapses. All ATRA naive patients achieved CR. Group 2: second or subsequent remission or in first relapse but received ATRA within 1 year before enrollment.

These 2 patients were newly diagnosed who had failed oral ATRA and were switched to the liposomal form.

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