Table 1.

Patient demographics and disease characteristics

Baseline characteristicTI-R (n = 14)TI-NR (n = 27)*TI-R vs TI-NROverall (N = 41)
Age, y 65 (10.0) 72 (7.5) nt 70 (9.0) 
 ≥65, n (%) 7 (50.0) 23 (85.2) P = .070 30 (73.2) 
Males, n (%) 8 (57.1) 18 (66.7) ns 26 (63.4) 
Race, n (%)   ns  
 White 11 (78.6) 25 (92.6)  36 (87.8) 
 Non-White 3 (21.4) 2 (7.4)  5 (12.2) 
Body mass index, kg/m2 28.9 (5.20) 25.3 (4.05) nt 26.5 (4.74) 
Type of MF, n (%)   ns  
 PMF 11 (78.6) 21 (77.8)  32 (78.0) 
 Post-PV/ET MF 3 (21.4) 6 (22.2)  9 (22.0) 
Time since MF diagnosis, y 3.0 (1.96) 3.4 (3.15) nt 3.3 (2.78) 
RBC units transfused ≤8 wk prior to enrollment 5 (1.9) 7 (2.2) nt 6 (2.3) 
Bone marrow fibrosis grade, n (%)   nt  
 0 or 1 2 (7.4)  2 (4.9) 
 2 1 (7.1) 5 (18.5)  6 (14.6) 
 3 12 (85.7) 18 (66.7)  30 (73.2) 
 Missing 1 (7.1) 2 (7.4)  3 (7.3) 
DIPSS risk level, n (%)   P = .075  
 Intermediate-1 4 (28.6) 1 (3.7)  5 (12.2) 
 Intermediate-2 8 (57.1) 14 (51.9)  22 (53.7) 
 High 2 (14.3) 12 (44.4)  14 (34.1) 
JAK2V617F mutation positive 9 (64.3) 19 (70.4) ns 28 (68.3) 
Hemoglobin, g/dL 8.8 (1.00) 8.1 (0.87) P = .036 8.3 (0.96) 
 Hemoglobin <8 2 (14.3) 10 (37.0)  12 (29.3) 
 Hemoglobin ≥8 12 (87.5) 17 (63.0)  29 (70.7) 
White blood cells, ×103/µL 7.2 (4.37) 15.2 (26.15) nt 12.50 (21.58) 
ANC, ×103/µL 5.28 (3.43) 11.97 (21.88) nt 9.68 (18.04) 
Platelet count, ×103/µL 233 (194.8) 155 (69.5) nt 181 (129.9) 
Spleen volume, cm3 2132.2 (1439.5) 2018.1 (1248.5) ns 2057.1 (1299.8) 
TSS 19.00 (16.14) 21.73 (13.97) ns 20.73 (14.65) 
CRP, mg/dL 1.4 (1.6) 2.5 (2.3) nt 2.2 (2.1) 
EPO, mIU/mL 293 (272) 522 (925) nt 444 (770) 
Ferritin, ng/mL 710 (471) 1648 (1507) nt 1328 (1324) 
Liver iron content, mg/g 3.6 (3.4) 7.6 (8.2) ns 6.2 (7.2) 
Hepcidin, nM     
 Morning 22.8 (15.14) 44.3 (24.80) P = .013 36.9 (24.09) 
 Afternoon 24.5 (11.59) 43.8 (22.50) nt 37.2 (21.40) 
Hepcidin daily change, nM 0.0 (5.52) −0.9 (7.80) nt −0.6 (7.04) 
Baseline characteristicTI-R (n = 14)TI-NR (n = 27)*TI-R vs TI-NROverall (N = 41)
Age, y 65 (10.0) 72 (7.5) nt 70 (9.0) 
 ≥65, n (%) 7 (50.0) 23 (85.2) P = .070 30 (73.2) 
Males, n (%) 8 (57.1) 18 (66.7) ns 26 (63.4) 
Race, n (%)   ns  
 White 11 (78.6) 25 (92.6)  36 (87.8) 
 Non-White 3 (21.4) 2 (7.4)  5 (12.2) 
Body mass index, kg/m2 28.9 (5.20) 25.3 (4.05) nt 26.5 (4.74) 
Type of MF, n (%)   ns  
 PMF 11 (78.6) 21 (77.8)  32 (78.0) 
 Post-PV/ET MF 3 (21.4) 6 (22.2)  9 (22.0) 
Time since MF diagnosis, y 3.0 (1.96) 3.4 (3.15) nt 3.3 (2.78) 
RBC units transfused ≤8 wk prior to enrollment 5 (1.9) 7 (2.2) nt 6 (2.3) 
Bone marrow fibrosis grade, n (%)   nt  
 0 or 1 2 (7.4)  2 (4.9) 
 2 1 (7.1) 5 (18.5)  6 (14.6) 
 3 12 (85.7) 18 (66.7)  30 (73.2) 
 Missing 1 (7.1) 2 (7.4)  3 (7.3) 
DIPSS risk level, n (%)   P = .075  
 Intermediate-1 4 (28.6) 1 (3.7)  5 (12.2) 
 Intermediate-2 8 (57.1) 14 (51.9)  22 (53.7) 
 High 2 (14.3) 12 (44.4)  14 (34.1) 
JAK2V617F mutation positive 9 (64.3) 19 (70.4) ns 28 (68.3) 
Hemoglobin, g/dL 8.8 (1.00) 8.1 (0.87) P = .036 8.3 (0.96) 
 Hemoglobin <8 2 (14.3) 10 (37.0)  12 (29.3) 
 Hemoglobin ≥8 12 (87.5) 17 (63.0)  29 (70.7) 
White blood cells, ×103/µL 7.2 (4.37) 15.2 (26.15) nt 12.50 (21.58) 
ANC, ×103/µL 5.28 (3.43) 11.97 (21.88) nt 9.68 (18.04) 
Platelet count, ×103/µL 233 (194.8) 155 (69.5) nt 181 (129.9) 
Spleen volume, cm3 2132.2 (1439.5) 2018.1 (1248.5) ns 2057.1 (1299.8) 
TSS 19.00 (16.14) 21.73 (13.97) ns 20.73 (14.65) 
CRP, mg/dL 1.4 (1.6) 2.5 (2.3) nt 2.2 (2.1) 
EPO, mIU/mL 293 (272) 522 (925) nt 444 (770) 
Ferritin, ng/mL 710 (471) 1648 (1507) nt 1328 (1324) 
Liver iron content, mg/g 3.6 (3.4) 7.6 (8.2) ns 6.2 (7.2) 
Hepcidin, nM     
 Morning 22.8 (15.14) 44.3 (24.80) P = .013 36.9 (24.09) 
 Afternoon 24.5 (11.59) 43.8 (22.50) nt 37.2 (21.40) 
Hepcidin daily change, nM 0.0 (5.52) −0.9 (7.80) nt −0.6 (7.04) 

Data are mean (standard deviation) unless otherwise noted.

ANC, absolute neutrophil count; EPO, erythropoietin; ET, essential thrombocythemia; ns, not significant (P > .1); nt, not tested; PMF, primary myelofibrosis; PV, polycythemia vera.

*

One patient enrolled without a confirmed transfusion history and was categorized as a TI-NR at week 24.

Significance was tested using a logistic regression model approach.

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