Skip to main content
. 2017 Mar 10;7(3):e538. doi: 10.1038/bcj.2017.17

Table 1. Presenting clinical and laboratory features of 262 patients with polycythemia vera stratified by the presence of grade 1 or greater bone marrow reticulin fibrosis.

Variables All patients (n=262) Patient without BM reticulin fibrosis (n=135, 52%) Patients withgrade 1 BM reticulin fibrosis (n=127, 48%) P-value
Age at referal in years; median (range) 62 (17–94) 64 (20–88) 60 (17–94) 0.08
Age⩾60, n (%) 141 (54%) 79 (59%) 62 (49%) 0.1
Male (%) 131 (50%) 69 (51%) 62 (49%) 0.7
Hemoglobin, g/dl median (range) 18 (14.8–24) 18 (15.8–23) 18 (14.8–24) 0.9
Leukocytes, × 109/l; median (range) 11.7 (4.3–59.3) 11.7 (4.7–59.3) 11.5 (4.3–35.5) 0.6
Leukocytes⩾11x109/l; median (range) 142 (57%) 73 (56%) 69 (59%) 0.6
Leukocytes⩾15x109/l; median (range) 58 (23%) 33 (25%) 25 (21%) 0.5
Platelets, × 109/l; median (range) 454 (44–2747) 456 (78–1720) 450 (44–2747) 0.4
Platelets⩾1.000 x109/l; median (range) 14 (6%) 9 (7%) 5 (4%) 0.3
Presence of palpable splenomegalyn (%) N evaluable=233 60 (26%) 28 (23%) 32 (29%) 0.3
Presence of pruritus n (%) N evaluable=253 83 (33%) 40 (31%) 43 (35%) 0.5
Presence of erythromelagia n (%) N evaluable=226 14 (6%) 6 (6%) 8 (7%) 0.7
         
WHO PV risk stratification       0.07
 Low risk 81 (31%) 35 (26%) 46 (36%)  
 High risk 181 (69%) 100 (74%) 81 (64%)  
         
Thrombosis history at diagnosis 74 (28%) 40 (30%) 34 (27%) 0.6
Thrombotic events after diagnosis 59 (23%) 31 (23%) 28 (22%) 0.9
         
Cytogenetics categories N evaluable=142        
 Normal cytogenetic 115 (81%) 64 (83%) 51 (78%) 0.5
 Favorable cytogenetica 136 (96%) 73 (95%) 63 (97%) 0.5
         
JAK2 n (%) N evaluable=258 250 (97%) 128 (96%) 122 (98%) 0.2
TET2 n (%) N evaluable=80 16 (20%) 11 (23%) 5 (15%) 0.4
ASXL1 n (%) N evaluable=80 8 (10%) 6 (13%) 2 (6%) 0.3

Abbreviations: BM, bone marrow; PV, polycythemia vera; WHO, World Health Organization.

a

Favorable karyotype: normal karyotype or sole or two abnormalities that do not include the below-listed unfavorable cytogenetic abnormalities. Unfavorable karyotype: complex karyotype or sole or two abnormalities that include +8, 7/7q-, i(17q), 5/5q-, 12p-, inv(3) or 11q23 rearrangement.