Table 3.

Results of multivariate Cox proportional hazards model of OS

CovariatePrimary and secondary MFOvert PMFPre-PMFPost-PV/ET MF
HR (95% CI)PHR (95% CI)PHR (95% CI)PHR (95% CI)P
Constitutional symptoms NS  NS  NS  NS  
Leukocytes >25 × 109/L 4.81 (2.79-8.26) <.0001 4.58 (1.90-11.01) .0007 18.28 (4.69-71.21) <.0001   
Hemoglobin <10 g/dL 2.27 (1.48-3.48) .0002 NS  2.61 (1.01-6.81) .0487 2.75 (1.54-4.91) .0006 
Blood blasts ≥2% 1.80 (1.10-2.96) .0204 2.52 (1.17-5.46) .0186 NS  2.90 (1.56-5.42) .0008 
Platelet count <100 × 109/L 4.79 (2.72-8.44) <.0001 4.80 (2.09-11.00) .0002 7.98 (2.33-27.36) .0010 8.25 (3.45-19.74) <.0001 
BM fibrosis grade ≥2 NS  —  —  —  
Absence of CALR1-like NS  NS  NS  NS  
HMRMT* 1.86 (1.24-2.80) .0029 NS  11.16 (3.53-35.28) <.0001 NS  
≥2 HMRMTs NS  NS  NS  NS  
RAS/CBLMT 1.73 (1.10-2.71) .0177 2.91 (1.54-5.50) .0010 NS  NS  
Cytogenetics         
 Favorable Reference  Reference  Reference  Reference  
 Unfavorable NS  2.39 (1.08-5.28) .0314 NS  NS  
 Very high risk 4.25 (2.27-7.98) <.0001 10.82 (3.57-32.76) <.0001 20.33 (4.58-90.31) <.0001 NS  
CovariatePrimary and secondary MFOvert PMFPre-PMFPost-PV/ET MF
HR (95% CI)PHR (95% CI)PHR (95% CI)PHR (95% CI)P
Constitutional symptoms NS  NS  NS  NS  
Leukocytes >25 × 109/L 4.81 (2.79-8.26) <.0001 4.58 (1.90-11.01) .0007 18.28 (4.69-71.21) <.0001   
Hemoglobin <10 g/dL 2.27 (1.48-3.48) .0002 NS  2.61 (1.01-6.81) .0487 2.75 (1.54-4.91) .0006 
Blood blasts ≥2% 1.80 (1.10-2.96) .0204 2.52 (1.17-5.46) .0186 NS  2.90 (1.56-5.42) .0008 
Platelet count <100 × 109/L 4.79 (2.72-8.44) <.0001 4.80 (2.09-11.00) .0002 7.98 (2.33-27.36) .0010 8.25 (3.45-19.74) <.0001 
BM fibrosis grade ≥2 NS  —  —  —  
Absence of CALR1-like NS  NS  NS  NS  
HMRMT* 1.86 (1.24-2.80) .0029 NS  11.16 (3.53-35.28) <.0001 NS  
≥2 HMRMTs NS  NS  NS  NS  
RAS/CBLMT 1.73 (1.10-2.71) .0177 2.91 (1.54-5.50) .0010 NS  NS  
Cytogenetics         
 Favorable Reference  Reference  Reference  Reference  
 Unfavorable NS  2.39 (1.08-5.28) .0314 NS  NS  
 Very high risk 4.25 (2.27-7.98) <.0001 10.82 (3.57-32.76) <.0001 20.33 (4.58-90.31) <.0001 NS  

NS, not significant.

*

The HMR category is defined as the presence of a mutation in any of the following genes: ASXL1, EZH2, SRSF2, and IDH1/2.

≥2 HMRMTs indicate the presence of 2 or more mutations in the ASXL1, EZH2, SRSF2, and IDH1/2 genes (2 or more mutations in the same gene are counted as 1).

According to the revised cytogenetic risk stratification.24 

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