Table 1

A comparison of clinical characteristics with stimulated pSTAT5 in primary CMML samples

Variable TypeMean (95%CI) stimulated pSTAT5%+Mean (95%CI) stimulated pSTAT5 FIPearson R (95%CI) stimulated pSTAT5%+Pearson R (95%CI) stimulated pSTAT5 FIP value: FI, %+
Categorical variables      
 WHO (–0.1492 to 0.06385) (–0.3307 to 0.1520)   .41, .47 
  CMML-1 (n = 15) 0.1713 0.3287    
  CMML-2 (n = 5) 0.2140 0.4180    
 IPSS35  (–0.1791 to 0.04663) (–0.3739 to 0.1451)   .23, .37 
  Lower (n = 16) 0.1688 0.3281    
  Higher (n = 4) 0.2350 0.4425    
 MDASC36  (–0.1829 to −0.02400) (–0.4178 to −0.06338)   .014, .011 
  Lower (n = 11) 0.1355 0.2427    
  Higher (n = 9) 0.2389 0.4833    
 MDAPS37  (–0.1948 to 0.02476) (–0.4887 to −0.02133)   .12, .034 
  Lower (n = 16) 0.1650 0.3000    
  Higher (n = 4) 0.2500 0.5550    
 DUSS38  (–0.1996 to 0.05369) (–0.4552 to 0.1156)   .24, .23 
  Lower (n = 15) 0.1200 0.2067    
  Higher (n = 5) 0.1929 0.3767    
 CYTO (–0.1139 to 0.09102) (–0.2160 to 0.2474)   .82, .88 
  Abnormal (n = 6) 0.1900 0.3557    
  Normal (n = 14) 0.1786 0.3400    
 Spleen (–0.09002 to 0.09802) (–0.2400 to 0.1840)   .93, .78 
  Enlarged (n = 10) 0.1840 0.3370    
  Normal (n = 10) 0.1800 0.3650    
 Mutations (*(*  * 
  Data available (n = 18) 0.1411 0.1712    
  No data available (n = 2) 0.1400 0.3700    
 Mutations (–0.1119 to 0.4736) (–0.1991 to 0.2818)   .72, .80 
  Present (n = 13) 0.4159 0.2288    
  Absent (n = 5) 0.2350 0.1875    
 RUNX1 (–0.4310 to 0.2487) (–0.3627 to 0.1571)   .41, .58 
  Mutation (n = 3) 0.3033 0.1267    
  No mutation (n = 15) 0.3944 0.2295    
 Signaling (0.06052 to 0.4501) (–0.009515 to 0.3874)   .055, .037 
  Mutation (n = 7) 0.5071 0.3271    
  No mutation (n = 9) 0.2518 0.1382    
 Epigenetic (–0.1441 to 0.3358) (–0.08641 to 0.3514)   .81, 1.00 
  Mutation (n = 6) 0.4150 0.3000    
  No mutation (n = 11) 0.3192 0.1675    
 Splicing (–0.2634 to 0.2927) (–0.2756 to 0.2456)   .87, .75 
  Mutation (n = 4) 0.3625 0.2000    
  No mutation (n = 14) 0.3479 0.2150    
Continuous variables      
 WBC   0.4984 (0.07155 to 0.7709) 0.3117 (−0.1519 to 0.6628) .025, .18 
 MONO   0.5875 (0.1958 to 0.8175) 0.3974 (−0.05482 to 0.7144) .006, .083 
 HGB   −0.05400 (−0.4850 to 0.3981) −0.1823 (−0.5783 to 0.2831) .82, .44 
 PLT   −0.1981 (−0.5891 to 0.2680) −0.2525 (−0.6252 to 0.2140) .40, .28 
 BM BLAST %   0.1942 (−0.2718 to 0.5864) 0.1819 (−0.2836 to 0.5779) .41, .44 
 Age   0.2611 (−0.2052 to 0.6308) 0.2467 (−0.2200 to 0.6214) .27, .29 
Variable TypeMean (95%CI) stimulated pSTAT5%+Mean (95%CI) stimulated pSTAT5 FIPearson R (95%CI) stimulated pSTAT5%+Pearson R (95%CI) stimulated pSTAT5 FIP value: FI, %+
Categorical variables      
 WHO (–0.1492 to 0.06385) (–0.3307 to 0.1520)   .41, .47 
  CMML-1 (n = 15) 0.1713 0.3287    
  CMML-2 (n = 5) 0.2140 0.4180    
 IPSS35  (–0.1791 to 0.04663) (–0.3739 to 0.1451)   .23, .37 
  Lower (n = 16) 0.1688 0.3281    
  Higher (n = 4) 0.2350 0.4425    
 MDASC36  (–0.1829 to −0.02400) (–0.4178 to −0.06338)   .014, .011 
  Lower (n = 11) 0.1355 0.2427    
  Higher (n = 9) 0.2389 0.4833    
 MDAPS37  (–0.1948 to 0.02476) (–0.4887 to −0.02133)   .12, .034 
  Lower (n = 16) 0.1650 0.3000    
  Higher (n = 4) 0.2500 0.5550    
 DUSS38  (–0.1996 to 0.05369) (–0.4552 to 0.1156)   .24, .23 
  Lower (n = 15) 0.1200 0.2067    
  Higher (n = 5) 0.1929 0.3767    
 CYTO (–0.1139 to 0.09102) (–0.2160 to 0.2474)   .82, .88 
  Abnormal (n = 6) 0.1900 0.3557    
  Normal (n = 14) 0.1786 0.3400    
 Spleen (–0.09002 to 0.09802) (–0.2400 to 0.1840)   .93, .78 
  Enlarged (n = 10) 0.1840 0.3370    
  Normal (n = 10) 0.1800 0.3650    
 Mutations (*(*  * 
  Data available (n = 18) 0.1411 0.1712    
  No data available (n = 2) 0.1400 0.3700    
 Mutations (–0.1119 to 0.4736) (–0.1991 to 0.2818)   .72, .80 
  Present (n = 13) 0.4159 0.2288    
  Absent (n = 5) 0.2350 0.1875    
 RUNX1 (–0.4310 to 0.2487) (–0.3627 to 0.1571)   .41, .58 
  Mutation (n = 3) 0.3033 0.1267    
  No mutation (n = 15) 0.3944 0.2295    
 Signaling (0.06052 to 0.4501) (–0.009515 to 0.3874)   .055, .037 
  Mutation (n = 7) 0.5071 0.3271    
  No mutation (n = 9) 0.2518 0.1382    
 Epigenetic (–0.1441 to 0.3358) (–0.08641 to 0.3514)   .81, 1.00 
  Mutation (n = 6) 0.4150 0.3000    
  No mutation (n = 11) 0.3192 0.1675    
 Splicing (–0.2634 to 0.2927) (–0.2756 to 0.2456)   .87, .75 
  Mutation (n = 4) 0.3625 0.2000    
  No mutation (n = 14) 0.3479 0.2150    
Continuous variables      
 WBC   0.4984 (0.07155 to 0.7709) 0.3117 (−0.1519 to 0.6628) .025, .18 
 MONO   0.5875 (0.1958 to 0.8175) 0.3974 (−0.05482 to 0.7144) .006, .083 
 HGB   −0.05400 (−0.4850 to 0.3981) −0.1823 (−0.5783 to 0.2831) .82, .44 
 PLT   −0.1981 (−0.5891 to 0.2680) −0.2525 (−0.6252 to 0.2140) .40, .28 
 BM BLAST %   0.1942 (−0.2718 to 0.5864) 0.1819 (−0.2836 to 0.5779) .41, .44 
 Age   0.2611 (−0.2052 to 0.6308) 0.2467 (−0.2200 to 0.6214) .27, .29 

Overall Cohort (n = 20).

WBC, white blood cell count at time of sample; HGB, hemoglobin level at time of sample; PLT, platelet count at time of sample; MONOS, peripheral monocyte count at time of sample; BLAST, percent myeloblast in the bone marrow aspiration differential; CYTO, cytogenetics at time of sample (abnormal or not); Spleen, spleen enlarged at any time.

Categorical variables were analyzed using the unpaired Student t test with Welch’s correction. Continuous variables were analyzed using the Pearson model.

*

Number too small for statistics.

No DNA available (2 of 20).

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