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. 2017 Oct 17;8(61):103274–103282. doi: 10.18632/oncotarget.21870

Table 1. Comparison of diagnostic categories, splenomegaly, treatment, and disease progression in patients without BM fibrosis to those with any amount of BM fibrosis.

MF-0 (N = 38) MF1+ (N = 45) P
Mean Age (Range) 70.1 41–90 66.6 23–87 0.1
M 23 61% 28 62% 1
F 15 39% 17 38%
CMML Category
1 32 86% 39 91% 0.5
2 5 14% 4 9%
CMML Type
MPN-type 20 53% 27 60% 0.6
MDS-type 18 47% 18 40%
Splenomegaly
Y 11/38 29% 26/45 58% 0.016
Disease Progression 6/33 18% 22/44 50% 0.005
Median Time to Disease Progression (m) NR 28.3 0.001
Median overall survival (m) 48.3 41.7 0.1
Treatment
Observation 10/33 31% 11/44 25% 0.95
Hypomethylating agents 13/33 39% 19/44 43%
JAK inhibitor 1/33 3% 1/44 2%
SCT 9/33 27% 13/44 30%
Outcome
DOD 9 24% 21 47% 0.6
ANED or AWD 12 32% 7 16%
LFU or DUC or DUD 17 45% 17 38%

NR = not reached, SCT = stem cell transplant, DOD = died of disease, ANED = alive no evidence of disease, AWD = alive with disease, DUC = died of unknown cause, DUD = died of unrelated disease, LFU = lost to follow up.