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. Author manuscript; available in PMC: 2025 Aug 25.
Published in final edited form as: Am J Hematol. 2017 Nov 27;93(2):277–285. doi: 10.1002/ajh.24972

TABLE 1.

Baseline characteristics (N = 35)

Characteristics N (%)/Median [range]
Age, years 70 [43–79]
 >65 years 23 (66)
Male 21 (60)
Diagnosis
 MDS/MPNU/CMML/aCML 14 (40)/17 (49)/4 (11)
MF DIPSS
Int-1/Int-2/High 7 (20)/18 (51)/10 (29)
MDS IPSS
 Low/Int-1/Int-2/High 14 (40)/14 (40)/6 (17)/1 (3)
MDS R-IPSS
 Very Low/Low/Int/High/ 8 (23)/12 (34)/10
 Very High    (28)/3 (9)/2 (6)
MDA Global score
 Low/Int-1/Int-2/High 3 (9)/20 (57)/9 (25)/3 (9)
Splenomegaly 12/32 (38%)
Peripheral blood blasts ≥1% 24 (69)
WBC [×109/L] 26.3 [3–123.2]
Platelets [×109/L] 170 [53–1429]
Hemoglobin [g/dL] 10.1 [6.4–14.4]
LDH 860 [409–3230]
Cytogenetics
 Diploid/Abnormal 25 (71)/10 (29)
EUMNET Fibrosis Grade
 MF-1/MF-2/MF-3 17/29 (59)/8/29
   (28)/4/29 (14)
Patients with prior treatment 12 (34)
JAK2 mutation 10 (29)
JAK2 allele burden (%) 42.2 [3–90]
CALR mutation 0/8
MPL mutation 1/34 (3)
Molecular (28-gene profile, N = 34) a
 ASXL1 7(21)
 TET2 6(18)
 KRAS 5(15)
 NRAS 4(12)
 DNMT3A 4 (12)
 PTPN11 3(9)
 IDH2 2 (6)
 RUNX1 1 (3)
 GATA2 1 (3)
a

Frequently identified mutations.

Abbreviations; Int: Intermediate; MDA: MD Anderson; WBC: white blood cell count; LDH: Lactate dehydrogenase; EUMNET: European myelofibrosis network.