Table 1.

Clinical and laboratory characteristics of 414 patients with primary myelofibrosis studied for serum albumin level and 318 patients studied for serum total cholesterol

CharacteristicSerum albumin <4.3 g/dL (n = 285),Serum albumin ≥4.3 g/dL (n = 129),PSerum total cholesterol <122 mg/dL (n = 119),Serum total cholesterol ≥122 mg/dL (n = 199),P
n (%)n (%)n (%)n (%)
Age, y       
 Median (range) 67 (22-92) 61 (19-84) <.001 64 (26-86) 61 (19-88) .02 
 >65 157 (55) 44 (34) <.001 53 (45) 79 (40) .4 
Males 182 (64) 71 (55) .09 93 (78) 108 (54) <.001 
Hemoglobin <10 g/dL 172 (60) 42 (33) <.001 68 (57) 78 (39) .002 
Requiring transfusion 121 (43) 29 (23) <.001 48 (40) 46 (23) .001 
Leukocytes >25 × 109/L 56 (20) 10 (8) .001 20 (17) 26 (13) .36 
Platelets <100 × 109/L 87 (31) 23 (18) .006 29 (24) 45 (23) .72 
Circulating blasts ≥1% 156 (55) 44 (34) <.001 73 (61) 87 (44) .002 
Constitutional symptoms 113 (40) 26 (20) <.001 50 (42) 45 (23) <.001 
DIPSS risk distribution*   <.001   <.001 
 High 46 (16) 2 (1.6)  14 (12) 13 (7)  
 Intermediate-2 126 (44) 39 (30)  66 (56) 65 (33)  
 Intermediate-1 96 (34) 54 (42)  26 (22) 76 (38)  
 Low 17 (6) 34 (26)  13 (11) 45 (23)  
DIPSS-plus risk distribution (no. evaluable: 411 [albumin]; 316 [cholesterol])   < .001   <.001 
 High 123 (43) 23 (18)  50 (42) 50 (25)  
 Intermediate-2 109 (38) 46 (36)  46 (39) 65 (33)  
 Intermediate-1 37 (13) 29 (23)  12 (10) 41 (21)  
 Low 15 (5) 29 (23)  11 (9) 41 (21)  
Driver mutations (no. evaluable: 277 [albumin]; 234 [cholesterol])   .67   .005 
 JAK2 122 (69) 63 (64)  64 (75) 83 (56)  
 CALR type 1–like 31 (17) 21 (21)  5 (6) 34 (23)  
 CALR type 2–like 6 (3) 2 (2)  3 (4) 7 (5)  
 MPL 7 (4) 7 (7)  3 (4) 9 (6)  
 Triple-negative 12 (7) 6 (6)  10 (12) 16 (11)  
Revised cytogenetic risk distribution (no. evaluable: 389 [albumin]; 303 [cholesterol])   .14   .12 
 Very high risk 29 (11) 6 (5)  8 (7) 5 (3)  
 Unfavorable 43 (16) 22 (18)  14 (12) 32 (17)  
 Favorable 196 (73) 93 (77)  95 (81) 149 (80)  
ASXL1-mutated (no. evaluable: 201 [albumin]; 191 [cholesterol]) 51 (40) 20 (27) .06 42 (58) 39 (33) <.001 
SRSF2-mutated (no. evaluable: 204 [albumin]; 191 [cholesterol]) 21 (16) 13 (17) P = .89 13 (18) 10 (8) .06 
CharacteristicSerum albumin <4.3 g/dL (n = 285),Serum albumin ≥4.3 g/dL (n = 129),PSerum total cholesterol <122 mg/dL (n = 119),Serum total cholesterol ≥122 mg/dL (n = 199),P
n (%)n (%)n (%)n (%)
Age, y       
 Median (range) 67 (22-92) 61 (19-84) <.001 64 (26-86) 61 (19-88) .02 
 >65 157 (55) 44 (34) <.001 53 (45) 79 (40) .4 
Males 182 (64) 71 (55) .09 93 (78) 108 (54) <.001 
Hemoglobin <10 g/dL 172 (60) 42 (33) <.001 68 (57) 78 (39) .002 
Requiring transfusion 121 (43) 29 (23) <.001 48 (40) 46 (23) .001 
Leukocytes >25 × 109/L 56 (20) 10 (8) .001 20 (17) 26 (13) .36 
Platelets <100 × 109/L 87 (31) 23 (18) .006 29 (24) 45 (23) .72 
Circulating blasts ≥1% 156 (55) 44 (34) <.001 73 (61) 87 (44) .002 
Constitutional symptoms 113 (40) 26 (20) <.001 50 (42) 45 (23) <.001 
DIPSS risk distribution*   <.001   <.001 
 High 46 (16) 2 (1.6)  14 (12) 13 (7)  
 Intermediate-2 126 (44) 39 (30)  66 (56) 65 (33)  
 Intermediate-1 96 (34) 54 (42)  26 (22) 76 (38)  
 Low 17 (6) 34 (26)  13 (11) 45 (23)  
DIPSS-plus risk distribution (no. evaluable: 411 [albumin]; 316 [cholesterol])   < .001   <.001 
 High 123 (43) 23 (18)  50 (42) 50 (25)  
 Intermediate-2 109 (38) 46 (36)  46 (39) 65 (33)  
 Intermediate-1 37 (13) 29 (23)  12 (10) 41 (21)  
 Low 15 (5) 29 (23)  11 (9) 41 (21)  
Driver mutations (no. evaluable: 277 [albumin]; 234 [cholesterol])   .67   .005 
 JAK2 122 (69) 63 (64)  64 (75) 83 (56)  
 CALR type 1–like 31 (17) 21 (21)  5 (6) 34 (23)  
 CALR type 2–like 6 (3) 2 (2)  3 (4) 7 (5)  
 MPL 7 (4) 7 (7)  3 (4) 9 (6)  
 Triple-negative 12 (7) 6 (6)  10 (12) 16 (11)  
Revised cytogenetic risk distribution (no. evaluable: 389 [albumin]; 303 [cholesterol])   .14   .12 
 Very high risk 29 (11) 6 (5)  8 (7) 5 (3)  
 Unfavorable 43 (16) 22 (18)  14 (12) 32 (17)  
 Favorable 196 (73) 93 (77)  95 (81) 149 (80)  
ASXL1-mutated (no. evaluable: 201 [albumin]; 191 [cholesterol]) 51 (40) 20 (27) .06 42 (58) 39 (33) <.001 
SRSF2-mutated (no. evaluable: 204 [albumin]; 191 [cholesterol]) 21 (16) 13 (17) P = .89 13 (18) 10 (8) .06 

Patients were stratified by ROC-determined cutoff points for albumin and total cholesterol. The values in bold indicate a significant P value (< .05).

*

DIPSS uses 5 independent predictors of inferior survival: age >65 years, hemoglobin <10 g/dL, leukocytes >25 × 109/L, circulating blasts ≥1%, and constitutional symptoms.

DIPSS-plus includes all the DIPSS variables plus 3 more: red cell transfusion need, platelet count <100 × 109/L, and unfavorable karyotype.

Revised cytogenetic risk stratification: very high risk includes single or multiple abnormalities of −7, i(17q), inv(3)/3q21, 12p-/12p11.2, 11q–/11q23, +21, or other autosomal trisomies, not including +8/+9; favorable risk includes normal karyotype or sole abnormalities of 13q–, +9, 20q–, chromosome 1 translocation, or duplication or sex chromosome abnormality including –Y; unfavorable risk includes all other abnormalities.

ASXL1, additional sex combs–like 1; CALR, calreticulin; JAK2, Janus kinase 2; MPL, myeloproliferative leukemia virus oncogene; SRSF2, serine/arginine-rich splicing factor 2.