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Table 5 Incidence of IDH mutations in AML patients from various countries

From: Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients

Country

No. IDH1m/all cases (%)

No. of IDH1m/CN-AML (%)

No. IDH2m/all cases (%)

No. of IDH2m/CN-AML (%)

ASIA

    

Taiwan

    

Chou W et al.(2010) [18]

27/493 (5.5)

20/227 (8.8)

ND

ND

China

    

Zou Y et al.(2010) [28]

4/68 (5.9)

ND

4/48 (8.3)

ND

Zhang Y et al.(2011) [32]

23/365 (6.3)

6/111 (5.4)

ND

ND

Lin J et al.(2011) [31]

4/110 (3.6)

ND

ND

ND

Thailand

    

This study

20/230 (8.7)

11/126 (8.7)

24/230 (10.4)

12/126 (9.5)

EUROPE‡[21, 23–27, 30, 41]

6.0-10.9

9.4-16.0

2.0*-10.9

3.2*-15.2

NORTH AMERICA ∫

2.2-13.7

4.9-16.0

1.3*-19.2

2.4*-19.2

[5, 15, 19, 20, 22, 29]

    
  1. *The authors only identified IDH2 R172K but did not include IDH2 R140Q mutation; † Pediatric acute myeloid leukemia; ‡ All studies reported during 2010-2011; ∫ All studies reported during 2009-2011; ND, not determined