Table 3.

Clinical and molecular characteristics of MPN cohorts with and without NGS

VariableCohort with NGS (n = 227)Cohort without NGS (n = 588)P
Age at diagnosis, mean ± SD, y 53.45 ± 15.8 50.56 ± 16.32 .020 
Male sex 117 (51.5) 229 (38.8) .001 
Phenotype at diagnosis    
 ET 106 (46.7) 275 (46.8) 1.000 
 PV 57 (25.1) 232 (39.4) <.001 
 PMF 64 (28.2) 81 (13.8) <.001 
MPN-specific mutation    
 JAK2+ 147 (64.8) 459 (78.1) <.001 
 CALR+ 56 (24.7) 73 (12.4) <.001 
 MPL+ 11 (4.8) 10 (1.7) .023 
 Triple negative 13 (5.7) 32 (5.4) .865 
 JAK2 others not done 0 (0) 14 (2.4) .014 
Karyotype    
 No lesion 41 (34.7) 184 (68.1) <.001 
 1 lesion 42 (35.6) 39 (14.4) <.001 
 ≥2 lesions 35 (29.7) 47 (17.4) .010 
Treatment with hydroxyurea 129 (56.8) 164 (27.9) <.001 
VariableCohort with NGS (n = 227)Cohort without NGS (n = 588)P
Age at diagnosis, mean ± SD, y 53.45 ± 15.8 50.56 ± 16.32 .020 
Male sex 117 (51.5) 229 (38.8) .001 
Phenotype at diagnosis    
 ET 106 (46.7) 275 (46.8) 1.000 
 PV 57 (25.1) 232 (39.4) <.001 
 PMF 64 (28.2) 81 (13.8) <.001 
MPN-specific mutation    
 JAK2+ 147 (64.8) 459 (78.1) <.001 
 CALR+ 56 (24.7) 73 (12.4) <.001 
 MPL+ 11 (4.8) 10 (1.7) .023 
 Triple negative 13 (5.7) 32 (5.4) .865 
 JAK2 others not done 0 (0) 14 (2.4) .014 
Karyotype    
 No lesion 41 (34.7) 184 (68.1) <.001 
 1 lesion 42 (35.6) 39 (14.4) <.001 
 ≥2 lesions 35 (29.7) 47 (17.4) .010 
Treatment with hydroxyurea 129 (56.8) 164 (27.9) <.001 

Data are expressed as n (%) unless otherwise indicated.

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