Table 10

Relationship of genetic aberrations and recurrent subtype aberrations to postrelapse survival

ParameterNonsurvivors (n = 15)Survivors (n = 28)P
Median postrelapse survival, d (range) 368* (6-1104) 1497* (371-3564) < .001* 
ACA, % positive 100* (6) 50* (12) .05* 
    +8/i(8q), cases — 
    Balanced translocation, cases — 
    Complex karyotype, cases — 
PRα/LBD mutations, % positive 40 39 NS 
    Missense mutations, cases 11 NS 
    G289E/R, cases 3* 1* — 
    R276Q/W, cases — 
    Deletion mutations, cases 2* 0* — 
FLT3-ITD mutations, % positive 21* 46* (26) .18 
FLT3-D835 mutations, % positive 13 (24) NS 
ParameterNonsurvivors (n = 15)Survivors (n = 28)P
Median postrelapse survival, d (range) 368* (6-1104) 1497* (371-3564) < .001* 
ACA, % positive 100* (6) 50* (12) .05* 
    +8/i(8q), cases — 
    Balanced translocation, cases — 
    Complex karyotype, cases — 
PRα/LBD mutations, % positive 40 39 NS 
    Missense mutations, cases 11 NS 
    G289E/R, cases 3* 1* — 
    R276Q/W, cases — 
    Deletion mutations, cases 2* 0* — 
FLT3-ITD mutations, % positive 21* 46* (26) .18 
FLT3-D835 mutations, % positive 13 (24) NS 

Individual case data are detailed in supplemental Table 12. Numbers in brackets indicate the number of cases tested if less than total cases indicated by “n” in the NS corresponding column heading.

— indicates too few for analysis; and NS, no significant difference.

*

Distribution differences of possible interest between nonsurvivors and survivors.

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