Skip to main content
. 2019 Aug 14;103(5):491–499. doi: 10.1111/ejh.13315

Table 2.

Patient characteristics of best supportive care and curative‐intent groups

Characteristic Curative (n = 50) Best supportive care (n = 33)  
Outcome—no. (%)
Deceased 37 (74) 33 (100)  
Survived 13 (26) 0 (0)
Sex—no. (%)
Male 29 (58) 17 (48.5) P = .561
Female 21 (42) 16 (51.5)
Age at time of allogeneic HSCT—y
Median (interquartile range) 53 (39‐58) 58 (50‐64) P = .043
Range 18‐71 26‐68
Prognostic class at time of AML diagnosis—no. (%)
Good risk 2 (4) 1 (3) Pearson's r = .226; P = .040
Intermediate risk 15 (30) 4 (12)
Poor risk 21 (42) 14 (42)
Very poor risk 12 (24) 14 (42)
WHO classification—no. (%)
AML with recurrent genetic abnormalities 19 (38) 14 (42)  
AML with myelodysplasia‐related changes 5 (10) 4 (12)
Therapy‐related myeloid neoplasms 3 (6) 3 (9)
AML NOS 21 (42) 11 (33)
Other 2 (4) 1 (3)
Transplantation type—no. (%)
MUD (10/10) 31 (62) 22 (67)  
SIB 8 (36) 10 (30)
CB 1 (2) 1 (3)
Conditioning regimen—no. (%)
Myeloablative 7 (14) 1 (3) P = .137
Reduced intensity or FLAMSA 43 (86) 32 (97)
Bone marrow blast count at time of relapse—% (n = 74)
Median (interquartile range) 21 (10‐50) 38 (20‐67) P = .025
Range 0‐74 10‐99
No data 4 5  
Time between allogeneic HSCT and relapse—wk
Median (interquartile range) 21 (14‐47) 21 (6‐28) P = .047
Range 5‐187 3‐63
Early vs late relapse—no. (%)
Early (<3 mo) 11 (22) 12 (36) P = .119
Late (≥3 mo) 39 (78) 21 (64)
Time between relapse and death—wk
Median (interquartile range) 16 (6‐31) 3 (1‐10) P < .001
Range 2‐119 0‐37

When n = 4 patients with isolated CNS relapse are excluded, the difference in bone marrow blast counts between the two groups is not significant.