Skip to main content
. 2014 Jan 9;105(1):97–104. doi: 10.1111/cas.12319

Table 5.

Clinical features and outcomes in acute promyelocytic leukemia (APL) patients with CD56 expression, as reported in published works

Authors No. of patients Treatment CD56+ APL (%) Clinical features in patients with CD56+ APL* CR rate
CIR
CIR (extramedullary)
DFS
OS
CD56+ CD56 CD56+ CD56 CD56+ CD56 CD56+ CD56 CD56+ CD56
Murray et al.9 50 CT alone / ATRA alone / ATRA + CT 24% S-isoform↑, Fibrinogen↓ 50%* 84% NA NA NA NA NA NA 5 weeks* 232 weeks
Ferrara et al.10 100 ATRA + CT 15% No effect 87% 94% NA NA 13% 8% 22 months NR 62%* 86%
Ito et al.11 28 ATRA + CT 14% Coexpression of CD34 100% 87% NA NA 75%* 0% 4 months* NR 26 months NR
Montesinos et al.12 651 CT alone / ATRA + CT 11% Initial WBC counts↑, Albumin↓, S-isoform↑, Coexpression of CD2, CD7, CD15, CD34, CD117, and HLA-DR 85% 92% 22%* 10% 7%* 1% 73%* 85% 78% 84%
Present study (all patients) 225 ATRA + CT 10% Initial platelet counts↓, Severe DIC↑, Coexpression of CD2, CD7, CD34, and HLA-DR 91% 95% 39% 24% 5% 1.5% 48% 65% 74% 79%
Present study (initial WBC counts ≥3.0 × 109/L) 112 ATRA + CT 12% 92% 94% 54%* 29% 9.3% 1.1% 31%* 64% 62% 79%
*

Significant difference.

Event-free survival in present study. APL, acute promyelocytic leukemia; ATRA, all-trans retinoic acid; CIR, cumulative incidence of relapse; CR, complete remission; CT, chemotherapy; DFS, disease-free survival; DIC, disseminated intravascular coagulation; HLA, human leukocyte antigen; NA, not available; NR, not reached; OS, overall survival; WBC, white blood cell.