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. 2016 Dec 21;129(10):1275–1283. doi: 10.1182/blood-2016-09-736686

Table 2.

Characteristics of relapsed acute promyelocytic leukemia patients

Patient no. Risk category Age (y) Sex Cytogenetics FLT3 status Time to first relapse (mo) Type of first relapse
1 High 52 F Diploid ND 9.2 Molecular*
2 Low 42 M 46XY t(15;17) [20] ND 79.5 Hematological/molecular
3 High 38 M 46XY t(15;17) [19] ND 9 Hematological/molecular
4 High 79 M 46XY t(15;17), der (17) i (17) (q10) [18]; 46 XY [2] Neg 12.4 Molecular*
5 High 18 M 46XY t(15;17) [19] ND 9.4 Molecular*
6 Low 19 F Diploid Neg 9.5 Hematological
7 High 35 M 46XY t(15;17) [16]; 46 idem, del 7 [1]; 46 XY [3] Neg 7.9 Hematological

BM, bone marrow; CNS, central nervous system; F, female; M, Male; MRD-SCT, matched-related donor stem cell transplantation; mo, months; No., number; ND, not done; Neg, negative.

*

Molecular relapses: Patient No.1 experienced a molecular relapse after 9.2 mo received salvage ATRA/ATO/GO achieved molecular remission, but then had a hematological relapse (BM+CNS) with time to hematological relapse of 18.8 mo (9.6 mo after molecular relapse). Patient No. 4 experienced a molecular relapse after 12.4 mo received salvage GO without achieving molecular remission and had a hematological relapse (CNS alone) with time to hematological relapse of 16.4 mo (4 mo after molecular relapse). Patient No. 5 experienced a molecular relapse after 9.4 mo received salvage ATRA/ATO/GO/IDA achieved molecular remission which was followed by MRD-SCT.