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. 2020 Nov 10;4(21):5562–5573. doi: 10.1182/bloodadvances.2020002727

Table 3.

Clinical significance of individual genetic mutations in multivariate analysis*

NRM Relapse PFS OS
Oncogenic variant n HR (95% CI) P HR (95% CI) P HR (95% CI) P HR (95% CI) P
TP53
 No 73 1.00 1.00 1.00 1.00
 Yes 22 0.66 (0.14-3.00) .59 2.59 (1.41-4.74) .002 2.18 (1.25-3.82) .006 1.99 (1.14-3.49) .02
JAK2
 No 43 1.00 1.00 1.00 1.00
 Yes 52 0.89 (0.37-2.15) .79 0.93 (0.56-1.56) .79 0.90 (0.57-1.41) .63 0.75 (0.47-1.19) .22
ASXL1
 No 74 1.00 1.00 1.00 1.00
 Yes 21 1.69 (0.66-4.32) .27 0.94 (0.51-1.74) .84 1.08 (0.62-1.88) .78 1.42 (0.85-2.38) .18
TET2
 No 77 1.00 1.00 1.00 1.00
 Yes 18 0.80 (0.26-2.43) .69 0.81 (0.41-1.60) .54 0.91 (0.50-1.66) .77 0.63 (0.33-1.19) .15
SRSF2
 No 80 1.00 1.00 1.00 1.00
 Yes 15 1.13 (0.41-3.16) .81 0.68 (0.32-1.45) .32 0.75 (0.39-1.42) .37 0.95 (0.50-1.79) .87
DNMT3A
 No 82 1.00 1.00 1.00 1.00
 Yes 13 1.31 (0.35-4.93) .69 1.04 (0.48-2.23) .92 0.85 (0.43-1.69) .65 1.22(0.63-2.33) .56
RUNX1
 No 82 1.00 1.00 1.00 1.00
 Yes 13 0.74 (0.20-2.71) .64 0.65 (0.31-1.39) .27 0.64 (0.32-1.29) .21 0.71 (0.37-1.37) .31
CALR
 No 83 1.00 1.00 1.00 1.00
 Yes 12 0.63 (0.08-4.90) .66 1.49 (0.75-2.98) .26 1.19 (0.60-2.35) .62 1.00 (0.52-1.94) 1.00
SF3B1
 No 85 1.00 1.00 1.00 1.00
 Yes 10 1.56 (0.50-4.86) .44 0.73 (0.29-1.84) .50 0.92 (0.44-1.93) .83 0.96 (0.46-1.99) .90
No. of gene mutations* 1.02 (0.83-1.24) .88 1.02 (0.85-1.22) .82 1.04 (0.87-1.25) .64

Each gene present in ≥10 patients was individually tested in multivariate analysis with the factors listed in the Appendix.

*

Tested as continuous variable.