成人急性髓系白血病新的基因突变与预后相关性研究进展

周念, 胡建达. 成人急性髓系白血病新的基因突变与预后相关性研究进展[J]. 临床血液学杂志, 2014, 27(1): 75-79. doi: 10.13201/j.issn.1004-2806.2014.01.023
引用本文: 周念, 胡建达. 成人急性髓系白血病新的基因突变与预后相关性研究进展[J]. 临床血液学杂志, 2014, 27(1): 75-79. doi: 10.13201/j.issn.1004-2806.2014.01.023
ZHOU Nian, HU Jianda. Research progress on new gene mutations and their prognostic significance in adult acute myeloid leukemia[J]. J Clin Hematol, 2014, 27(1): 75-79. doi: 10.13201/j.issn.1004-2806.2014.01.023
Citation: ZHOU Nian, HU Jianda. Research progress on new gene mutations and their prognostic significance in adult acute myeloid leukemia[J]. J Clin Hematol, 2014, 27(1): 75-79. doi: 10.13201/j.issn.1004-2806.2014.01.023

成人急性髓系白血病新的基因突变与预后相关性研究进展

详细信息
    通讯作者: 胡建达,E-mail:jdhu@medmail.com.cn
  • 中图分类号: R733.71

Research progress on new gene mutations and their prognostic significance in adult acute myeloid leukemia

More Information
  • 加载中
  • [1]

    LEY T J,DING L,WALTER M J,et al.DNMT3A mutations in acute myeloid leukemia[J].N Engl J Med,2010,363:2424-2433.

    [2]

    HOU H A,KUO Y Y,LIU C Y,et al.DNMT3A mutations in acute myeloid leukemia:stability during disease evolution and clinical implications[J].Blood,2012,119:559-568.

    [3]

    RIBEIRO A F,PRATCORONA M,ERPELINCK-VERSCHUEREN C,et al.Mutant DNMT3A:a marker of poor prognosis in acute myeloid leukemia[J].Blood,2012,119:5824-5831.

    [4]

    SHEN Y,ZHU YM,FAN X,et al.Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia[J].Blood,2011,118:5593-5603.

    [5]

    MARCUCCI G,METZELER K H,SCHWIND S,et al.Age-related prognostic impact of different types of DNMT3A mutations in adults with primary cytogenetically normal acute myeloid leukemia[J].J Clin Oncol,2012,30:742-750.

    [6]

    MARKOVA J,MICHKOVA P,BURCKOVA K,et al.Prognostic impact of DNMT3A mutations in patients with intermediate cytogenetic risk profile acute myeloid leukemia[J].Eur J Haematol,2012,88:128-135.

    [7]

    PATEL J P,GÖNEN M,FIGUEROA M E,et al.Prognostic relevance of integrated genetic profiling in acute myeloid leukemia[J].N Engl J Med,2012,366:1079-1089.

    [8]

    SCHNITTGER S,HAFERLACH C,ULKE M,et al.IDH1 mutations are detected in 6.6% of 1414 AML patients and are associated with intermediate risk karyotype and unfavorable prognosis in adults younger than 60 years and unmutated NPM1 status[J].Blood,2010,116:5486-5496.

    [9]

    RAVANDI F,PATEL K,LUTHRA R,et al.Prognostic significance of alterations in IDH enzyme isoforms in patients with AML treated with high-dose cytarabine and idarubicin[J].Cancer,2012,118:2665-2673.

    [10]

    GREEN C L,EVANS C M,HILLS R K,et al.The prognostic significance of IDH1 mutations in younger adult patients with acute myeloid leukemia is dependent on FLT3/ITD status[J].Blood,2010,116:2779-2782.

    [11]

    NOMDEDEU J,HOYOS M,CARRICONDO M,et al.Adverse impact of IDH1 and IDH2 mutations in primary AML:experience of the Spanish CETLAM group[J].Leuk Res,2012,36:990-997.

    [12]

    WAGNER K,DAMM F,GOHRING G,et al.Impact of IDH1 R132 mutations and an IDH1 single nucleotide polymorphism in cytogenetically normal acute myeloid leukemia:SNP rs11554137 is an adverse prognostic factor[J].J Clin Oncol,2010,28:2356-2364.

    [13]

    CHOU W C,LEI W C,KO B S,et al.The prognostic impact and stability of Isocitrate dehydrogenase 2 mutation in adult patients with acute myeloid leukemia[J].Leukemia,2011,25:246-253.

    [14]

    BOISSEL N,NIBOUREL O,RENNEVILLE A,et al.Prognostic impact of isocitrate dehydrogenase enzyme isoforms 1 and 2 mutations in acute myeloid leukemia:a study by the Acute Leukemia French Association group[J].J Clin Oncol,2010,28:3717-3723.

    [15]

    GREEN C L,EVANS C M,ZHAO L,et al.The prognostic significance of IDH2 mutations in AML depends on the location of the mutation[J].Blood,2011,118:409-412.

    [16]

    CHOU W C,CHOU S C,LIU CY,et al.TET2 mutation is an unfavorable prognostic factor in acute myeloid leukemia patients with intermediate-risk cytogenetics[J].Blood,2011,118:3803-3810.

    [17]

    KOSMIDER O,DELABESSE E,DE MAS V M,et al.TET2 mutations in secondary acute myeloid leukemias:a French retrospective study[J].Haematologica,2011,96:1059-1063.

    [18]

    GAIDZIK V I,PASCHKA P,SPATH D,et al.TET2 mutations in acute myeloid leukemia (AML):results from a comprehensive genetic and clinical analysis of the AML study group[J].J Clin Oncol,2012,30:1350-1357.

    [19]

    魏计锋,陈广华,仇惠英,等.急性髓系白血病患者TET2基因突变发生率及其临床意义[J].中华血液学杂志,2011,32(5):304-307.

    [20]

    METZELER K H,MAHARRY K,RADMACHER M D,et al.TET2 mutations improve the new European LeukemiaNet risk classification of acute myeloid leukemia:a Cancer and Leukemia Group B study[J].J Clin Oncol,2011,29:1373-1381.

    [21]

    CHOU W C,HUANG H H,HOU H A,et al.Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1(ASXL1) mutations[J].Blood,2010,116:4086-4094.

    [22]

    PRATCORONA M,ABBAS S,SANDERS M A,et al.Acquired mutations in ASXL1 in acute myeloid leukemia:prevalence and prognostic value[J].Haematologica,2012,97:388-392.

    [23]

    METZELER K H,BECKER H,MAHARRY K,et al.ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category[J].Blood,2011,118:6920-6929.

    [24]

    AWAD M M,ALADLE D A,ABOUSAMRA N K,et al.CEBPA gene mutations in Egyptian acute myeloid leukemia patients:impact on prognosis[J].Hematology,2013,18:61-68.

    [25]

    DUFOUR A,SCHNEIDER F,HOSTER E,et al.Monoallelic CEBPA mutations in normal karyotype acute myeloid leukemia:independent favorable prognostic factor within NPM1 mutated patients[J].Ann Hematol,2012,91:1051-1063.

    [26]

    GREIF P A,DUFOUR A,KONSTANDIN N P,et al.GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia[J].Blood,2012,120:395-403.

    [27]

    FASAN A,EDER C,HAFERLACH C,et al.GATA2 mutations are frequent in intermediate-risk karyotype AML with biallelic CEBPA mutations and are associated with favorable prognosis[J].Leukemia,2013,27:482-485.

    [28]

    SCHLENK R F,DOHNER K,KRAUTER J,et al.Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia[J].N Engl J Med,2008,358:1909-1918.

    [29]

    SCHNEIDER F,HOSTER E,SCHNEIDER S,et al.Age-dependent frequencies of NPM1 mutations and FLT3-ITD in patients with normal karyotype AML(NK-AML)[J].Ann Hematol,2012,91:9-18.

    [30]

    KRÖNKE J,SCHLENK R F,JENSEN K O,et al.Monitoring of minimal residual disease in NPM1-mutated acute myeloid leukemia:a study from the German-Austrian acute myeloid leukemia study group[J].J Clin Oncol,2011,29:2709-2716.

    [31]

    SCHNITTGER S,BACHER U,KERN W,et al.Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemia[J].Leukemia,2011,25:1297-1304.

    [32]

    SCHNEIDER F,HOSTER E,UNTERHALT M,et al.The FLT3ITD mRNA level has a high prognostic impact in NPM1 mutated,but not in NPM1 unmutated AML with a normal karyotype[J].Blood,2012,119:4383-4386.

    [33]

    SANTOS F P,JONES D,QIAO W,et al.Prognostic value of FLT3 mutations among different cytogenetic subgroups in acute myeloid leukemia[J].Cancer,2011,117:2145-2155.

    [34]

    HOU H A,HUANG T C,LIN LI,et al.WT1 mutation in 470 adult patients with acute myeloid leukemia:stability during disease evolution and mplication of its incorporation into a survival scoring system[J].Blood,2010,115:5222-5231.

    [35]

    GAIDZIK V I,SCHLENK R F,MOSCHNY S,et al.Prognostic impact of WT1 mutations in cytogenetically normal acute myeloid leukemia:a study of the German-Austrian AML Study Group[J].Blood,2009,113:4505-4511.

    [36]

    DAMM F,HEUSER M,MORGAN M,et al.Single nucleotide polymorphism in the mutational hotspot of WT1 predicts a favorable outcome in cytogenetically normal acute myeloid leukemia[J].J Clin Oncol,2010,28:578-585.

    [37]

    CHOI Y,LEE J H,HUR E H,et al.Single nucleotide polymorphism of Wilms' tumor 1 gene rs16754 in Korean patients with cytogenetically normal acute myeloid leukemia[J].Ann Hematol,2012,91:671-677.

    [38]

    MENDLER J H,MAHARRY K,RADMACHER M D,et al.RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and microRNA expression signatures[J].J Clin Oncol,2012,30:3109-3118.

    [39]

    GAIDZIK V I,BULLINGER L,SCHLENK R F,et al.RUNX1 mutations in acute myeloid leukemia:results from a comprehensive genetic and clinical analysis from the AML study group[J].J Clin Oncol,2011,29:1364-1372.

  • 加载中
计量
  • 文章访问数:  184
  • PDF下载数:  188
  • 施引文献:  0
出版历程
收稿日期:  2012-12-05

目录