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Table 1 Correlations between immunophenotypic markers and comutations for NPM1mut AML

From: The correlation of next-generation sequencing-based genotypic profiles with clinicopathologic characteristics in NPM1-mutated acute myeloid leukemia

Association

Entire cohort

NPM1mut/FLT3-ITD(−)

NPM1mut/FLT3-ITD(+)

χ2 P

OR (95% CI)

P

χ2 P

OR (95% CI)

P

χ2 P

OR (95% CI)

P

CD34 (N = 202)

×FLT3-ITD

< 0.001

5.29 (2.64–10.60)

< 0.001

NA

NA

NA

NA

NA

NA

×DNMT3A

0.026

NA

NA

NS

NA

NA

0.028

2.60 (1.00–6.79)

0.051

×TET2/IDH1

0.001

0.26 (0.11–0.62)

0.002

NS

NA

NA

0.005

0.21 (0.06–0.71)

0.012

CD7 (N = 186)

×FLT3-ITD

< 0.001

3.47 (1.79–6.73)

< 0.001

NA

NA

NA

NA

NA

NA

×DNMT3A

< 0.001

NA

NA

0.008

NA

NA

0.007

3.30 (1.15–9.46)

0.026

×DNMT3A-R882

< 0.001

3.59 (1.80–7.16)

< 0.001

0.002

3.93 (1.61–9.59)

0.003

0.009

NA

NA

×TET2/IDH1

NS

0.30 (0.14–0.62)

0.001

0.048

NA

NA

0.001

0.18 (0.05–0.60)

0.005

HLA-DR (N = 200)

×Ras pathways

< 0.001

4.05 (1.70–9.63)

0.002

0.002

3.83 (1.40–10.46)

0.009

0.055

NA

NA

×DNMT3A-R882

< 0.001

13.41 (4.56–39.45)

< 0.001

< 0.001

26.77 (3.44–208.46)

0.002

< 0.001

8.65 (2.28–32.89)

0.002

×TET2/IDH1

0.046

NA

NA

NS

NA

NA

0.002

0.26 (0.09–0.78)

0.016

MPO (N = 196)

×KRAS

0.003

0.18 (0.05–0.62)

0.007

0.002

0.13 (0.03–0.56)

0.006

NS

NA

NA

×DNMT3A

< 0.001

0.35 (0.17–0.70)

0.003

0.003

NA

NA

0.071

NA

NA

×DNMT3A-R882

0.001

NA

NA

0.002

0.27 (0.10–0.74)

0.011

NS

NA

NA

×TET2/IDH1

0.001

3.52 (1.48–8.38)

0.004

0.040

NA

NA

0.021

4.32 (1.16–16.15)

0.029

APL-like (N = 198)

×Ras pathways

< 0.001

0.22 (0.08–0.57)

0.002

0.008

0.32 (0.11–0.96)

0.041

0.025

NA

NA

×DNMT3A-R882

< 0.001

0.02 (0.00–0.18)

< 0.001

< 0.001

NA

NA

< 0.001

0.04 (0.01–0.36)

0.004

×TET2/IDH1

0.008

2.26 (1.07–4.78)

0.033

NS

NA

NA

< 0.001

6.73 (1.83–24.78)

0.004

  1. Abbreviations: OR odds ratio, CI confidence interval, NS not significant, NA not applicable; An OR of > 1 or < 1 means an independently positive or negative association, respectively, for patients with coexisting mutations compared with those with wild-type