Table 5

Risk factors investigated for their association with new nonmyeloid malignancy in ET and PV: distribution in case patients who developed a nonmyeloid cancer and control patients who did not

CharacteristicCases (n = 50)Controls (n = 221)P
ET/PV 30 (60%)/20 (40%) 150 (68%)/71 (32%) .3 
Median age, y (range) 64 (21-81) 53 (13-84) < .001 
Sex, male/female 21 (42%)/29 (58%) 75 (34%)/146 (66%) .3 
JAK2 mutation 34/45 (76%) 107/202 (53%) .008 
JAK2 genotype (rs12340895) 
    CC 21 (44%) 86 (40%) .3 
    CG 15 (31%) 106 (50%)  
    GG 12 (25%) 22 (10%)  
    GG/CC + CG (R) 12/49 (24%) 22/214 (10%) .01 
Exposure to cytoreductive agents 38 (76%) 164 (74%) .1 
DNA repair SNPs* 
    ERCC2 (XPD) Lys751Gln: CC/AA + AC (R) 11 (22%)/38 (78%) 20 (9%)/200 (91%) .007 
    ERCC5 Asp1104His: GC + CC/GG (D) 19 (40%)/29 (60%) 103 (50%)/105 (50%) .2 
    XPC Ala499Val: TT/CC + CT (R) 5 (10%)/44 (90%) 17 (8%)/197 (92%) .6 
    XPC Lys939Gln: AC + CC/AA (D) 29 (60%)/19 (40%) 141 (66%)/74 (34%) .5 
    XRCC1 Arg399Gln: GA + AA/GG (D) 24 (49%)/25 (51%) 134 (61%)/85 (39%) .1 
CharacteristicCases (n = 50)Controls (n = 221)P
ET/PV 30 (60%)/20 (40%) 150 (68%)/71 (32%) .3 
Median age, y (range) 64 (21-81) 53 (13-84) < .001 
Sex, male/female 21 (42%)/29 (58%) 75 (34%)/146 (66%) .3 
JAK2 mutation 34/45 (76%) 107/202 (53%) .008 
JAK2 genotype (rs12340895) 
    CC 21 (44%) 86 (40%) .3 
    CG 15 (31%) 106 (50%)  
    GG 12 (25%) 22 (10%)  
    GG/CC + CG (R) 12/49 (24%) 22/214 (10%) .01 
Exposure to cytoreductive agents 38 (76%) 164 (74%) .1 
DNA repair SNPs* 
    ERCC2 (XPD) Lys751Gln: CC/AA + AC (R) 11 (22%)/38 (78%) 20 (9%)/200 (91%) .007 
    ERCC5 Asp1104His: GC + CC/GG (D) 19 (40%)/29 (60%) 103 (50%)/105 (50%) .2 
    XPC Ala499Val: TT/CC + CT (R) 5 (10%)/44 (90%) 17 (8%)/197 (92%) .6 
    XPC Lys939Gln: AC + CC/AA (D) 29 (60%)/19 (40%) 141 (66%)/74 (34%) .5 
    XRCC1 Arg399Gln: GA + AA/GG (D) 24 (49%)/25 (51%) 134 (61%)/85 (39%) .1 
*

Results from the best inheritance model for each specific polymorphism. Genetic models: R indicates recessive; and D, dominant.

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