Table 1

Relapse study group parameters (n = 45)

ParameterNo. (%) or median (range)
Sex Male, 25 (56%); female, 20 (44%) 
Age, y 32 (1-68)* 
WBC, × 103/μL 6.8 (0.6-143) 
APL cytologic type M3, 37 (82%); M3 variant, 6 (13%) 
PML-RARα type S-isoform, 29 (64%); L-isoform, 16 (36%) 
Days to relapse 528 (134-1431) 
ATRA status at relapse§ On-ATRA, 20 (44%); Off-ATRA, 25 (56%) 
Postrelapse death Alive, 30 (67%); dead, 15 (33%) 
ParameterNo. (%) or median (range)
Sex Male, 25 (56%); female, 20 (44%) 
Age, y 32 (1-68)* 
WBC, × 103/μL 6.8 (0.6-143) 
APL cytologic type M3, 37 (82%); M3 variant, 6 (13%) 
PML-RARα type S-isoform, 29 (64%); L-isoform, 16 (36%) 
Days to relapse 528 (134-1431) 
ATRA status at relapse§ On-ATRA, 20 (44%); Off-ATRA, 25 (56%) 
Postrelapse death Alive, 30 (67%); dead, 15 (33%) 

For complete data on all 45 relapse patients, see supplemental Table 3.

*

Distribution: < 15 years, 11; 15-60 years, 28; and > 60 years, 6.

Distribution: < 5 × 103/μL, 43%; 5-10 ×103/μL, 16%; > 10 ×103/μL, 41%.

French-American-British subclassification ×103; 2 patients could not be subclassified.

§

On-ATRA, relapse within 30 days of last ATRA dose; Off-ATRA, relapse > 30 days after last ATRA dose (actual range, 86-966 days).

Median follow-up of surviving patients = 71 months.

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