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. 2017 Mar 29;5(5):645–653. doi: 10.1002/ccr3.919

Table 1.

APL relapse cases experienced in our institution between 1991 and 2015

Sex/Age (years) Cytogenesis WBC (x 109/L) Risk group (Sanz score) CD56 DS CNS prohylaxis PML‐RARA isoform CNS bleeding Time to 1st hematological relapse Time to CNS invavsion/relapse 1st induction therapy
M/68 46,XY,t(15;17)(q22;q21) 3.4 Intermediate N No No bcr3 No 16 M 16 M ATRA+CT
M/50 48,XY,+1,+8,del(11)(p 15)add(11) (q13),t(15;17)(q22;q21) 1.2 Low N No No NT No 14 M ATRA
F/22 46,XX,t(15;17)(q22;q21) 1.1 Low NT No No NT No 9 M CT
M/63 46,XY,t(15;17)(q22;q21) 0.5 Low P No No bcr3 No 10 M ATRA
F/49 46XX,t(15;17)(q22;q21) 15.2 High NT No No bcr3 No 14 M ATRA+CT
F/57 46,XX,t(15;17)(q22;q21) 0.8 Low N Yes No bcr3 No 13 M 90 M (54 M after allo‐SCT) ATRA+CT
M/70 46,XY,t(15;17)(q22;q12) 16.6 High P No Yes (TIT) NT Yes 30 M 30 M ATRA+CT

M in sex, male; F in sex, female; WBC, white blood cell count; CNS, central nervous system; APL, acute promyelocytic leukemia; DS, differentiation syndrome; TIT, triple intrathecal therapy; BM, bone marrow; CR, complete remission; ATRA, all‐trans retinoic acid; CT, chemotherapy; allo‐SCT, allogeneic stem cell transplantation; NT, not tested; M in time, month.