메뉴 건너뛰기




Volumn 11, Issue 4, 2016, Pages

A modified integrated genetic model for risk prediction in younger patients with acute myeloid leukemia

Author keywords

[No Author keywords available]

Indexed keywords

CD135 ANTIGEN; DNA METHYLTRANSFERASE 3A; ISOCITRATE DEHYDROGENASE 1; ISOCITRATE DEHYDROGENASE 2; NUCLEOPHOSMIN;

EID: 84962878143     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0153016     Document Type: Article
Times cited : (9)

References (29)
  • 1
    • 0034672269 scopus 로고    scopus 로고
    • Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: A Southwest Oncology Group/Eastern Cooperative Oncology Group Study
    • 11110676
    • Slovak ML, Kopecky KJ, Cassileth PA, Harrington DH, Theil KS, Mohamed A, et al. Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study. Blood. 2000;96:4075-4083. PMID: 11110676
    • (2000) Blood , vol.96 , pp. 4075-4083
    • Slovak, M.L.1    Kopecky, K.J.2    Cassileth, P.A.3    Harrington, D.H.4    Theil, K.S.5    Mohamed, A.6
  • 2
    • 77955914238 scopus 로고    scopus 로고
    • Refinement of cytogenetic classification in acute myeloid leukemia: Determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials
    • 20385793
    • Grimwade D, Hills RK, Moorman AV, Walker H, Chatters S, Goldstone AH, et al. Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials. Blood. 2010;116:354-365. doi: 10.1182/blood-2009-11-254441 PMID: 20385793
    • (2010) Blood , vol.116 , pp. 354-365
    • Grimwade, D.1    Hills, R.K.2    Moorman, A.V.3    Walker, H.4    Chatters, S.5    Goldstone, A.H.6
  • 3
    • 42949142189 scopus 로고    scopus 로고
    • Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
    • 18450602
    • Schlenk RF, Döhner K, Krauter J, Fröhling S, Corbacioglu A, Bullinger L, et al. Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia. N Engl J Med. 2008;358:1909-1918. doi: 10.1056/NEJMoa074306 PMID: 18450602
    • (2008) N Engl J Med , vol.358 , pp. 1909-1918
    • Schlenk, R.F.1    Döhner, K.2    Krauter, J.3    Fröhling, S.4    Corbacioglu, A.5    Bullinger, L.6
  • 4
    • 77954921625 scopus 로고    scopus 로고
    • Prognostic significance of CEBPA mutations in a large cohort of younger adult patients with acute myeloid leukemia: Impact of double CEBPA mutations and the interaction With FLT3 and NPM1 mutations
    • 20439648
    • Green CL, Koo KK, Hills RK, Burnett AK, Linch DC, Gale RE. Prognostic Significance of CEBPA Mutations in a Large Cohort of Younger Adult Patients With Acute Myeloid Leukemia: Impact of Double CEBPA Mutations and the Interaction With FLT3 and NPM1 Mutations. J Clin Oncol. 2010;28:2739-2747. doi: 10.1200/JCO.2009.26.2501 PMID: 20439648
    • (2010) J Clin Oncol. , vol.28 , pp. 2739-2747
    • Green, C.L.1    Koo, K.K.2    Hills, R.K.3    Burnett, A.K.4    Linch, D.C.5    Gale, R.E.6
  • 5
    • 79952122978 scopus 로고    scopus 로고
    • Prognostic impact, concurrent genetic mutations, and gene expression features of AML with CEBPA mutations in a cohort of 1182 cytogenetically normal AML patients: Further evidence for CEBPA double mutant AML as a distinctive disease entity
    • 21177436
    • Taskesen E, Bullinger L, Corbacioglu A, Sanders MA, Erpelinck C A J, Wouters BJ, et al. Prognostic impact, concurrent genetic mutations, and gene expression features of AML with CEBPA mutations in a cohort of 1182 cytogenetically normal AML patients: further evidence for CEBPA double mutant AML as a distinctive disease entity. Blood. 2011;117:2469-2475. doi: 10.1182/blood-2010-09-307280 PMID: 21177436
    • (2011) Blood , vol.117 , pp. 2469-2475
    • Taskesen, E.1    Bullinger, L.2    Corbacioglu, A.3    Sanders, M.A.4    Erpelinck, C.A.J.5    Wouters, B.J.6
  • 6
    • 0037114829 scopus 로고    scopus 로고
    • Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: A study of the AML Study Group Ulm
    • 12393388
    • Frohling S. Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: a study of the AML Study Group Ulm. Blood. 2002;100:4372-4380. doi: 10.1182/blood-2002-05-1440 PMID: 12393388
    • (2002) Blood , vol.100 , pp. 4372-4380
    • Frohling, S.1
  • 8
    • 84871774636 scopus 로고    scopus 로고
    • Prognostic significance of the European LeukemiaNet standardized system for reporting cytogenetic and molecular alterations in adults with acute myeloid leukemia
    • 22987078
    • Mrozek K, Marcucci G, Nicolet D, Maharry KS, Becker H, Whitman SP, et al. Prognostic Significance of the European LeukemiaNet Standardized System for Reporting Cytogenetic and Molecular Alterations in Adults With Acute Myeloid Leukemia. J Clin Oncol. 2012;30:4515-4523. doi: 10.1200/JCO.2012. 43.4738 PMID: 22987078
    • (2012) J Clin Oncol , vol.30 , pp. 4515-4523
    • Mrozek, K.1    Marcucci, G.2    Nicolet, D.3    Maharry, K.S.4    Becker, H.5    Whitman, S.P.6
  • 9
    • 77449159028 scopus 로고    scopus 로고
    • Diagnosis and management of acute myeloid leukemia in adults: Recommendations from an international expert panel, on behalf of the European LeukemiaNet
    • 19880497
    • Dohner H, Estey EH, Amadori S, Appelbaum FR, Buchner T, Burnett AK, et al. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet. Blood. 2010;115:453-474. doi: 10.1182/blood-2009-07-235358 PMID: 19880497
    • (2010) Blood , vol.115 , pp. 453-474
    • Dohner, H.1    Estey, E.H.2    Amadori, S.3    Appelbaum, F.R.4    Buchner, T.5    Burnett, A.K.6
  • 10
    • 79954428737 scopus 로고    scopus 로고
    • TET2 mutations improve the new european leukemianet risk classification of acute myeloid leukemia: A cancer and leukemia group B study
    • 21343549
    • Metzeler KH, Maharry K, Radmacher MD, Mrozek K, Margeson D, Becker H, et al. TET2 Mutations Improve the New European LeukemiaNet Risk Classification of Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study. J Clin Oncol. 2011;29:1373-1381. doi: 10.1200/JCO.2010.32.7742 PMID: 21343549
    • (2011) J Clin Oncol. , vol.29 , pp. 1373-1381
    • Metzeler, K.H.1    Maharry, K.2    Radmacher, M.D.3    Mrozek, K.4    Margeson, D.5    Becker, H.6
  • 11
    • 80053620171 scopus 로고    scopus 로고
    • TET2 mutation is an unfavorable prognostic factor in acute myeloid leukemia patients with intermediate-risk cytogenetics
    • 21828143
    • Chou W-C, Chou S-C, Liu C-Y, Chen C-Y, Hou H-A, Kuo Y-Y, et al. TET2 mutation is an unfavorable prognostic factor in acute myeloid leukemia patients with intermediate-risk cytogenetics. Blood. 2011;118:3803-3810. doi: 10.1182/blood-2011-02-339747 PMID: 21828143
    • (2011) Blood , vol.118 , pp. 3803-3810
    • Chou, W.-C.1    Chou, S.-C.2    Liu, C.-Y.3    Chen, C.-Y.4    Hou, H.-A.5    Kuo, Y.-Y.6
  • 12
    • 84255176496 scopus 로고    scopus 로고
    • ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category
    • 22031865
    • Metzeler KH, Becker H, Maharry K, Radmacher MD, Kohlschmidt J, Mrozek K, et al. ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category. Blood. 2011;118:6920-6929. doi: 10.1182/blood-2011-08-368225 PMID: 22031865
    • (2011) Blood , vol.118 , pp. 6920-6929
    • Metzeler, K.H.1    Becker, H.2    Maharry, K.3    Radmacher, M.D.4    Kohlschmidt, J.5    Mrozek, K.6
  • 14
    • 84863393263 scopus 로고    scopus 로고
    • Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
    • 22417203
    • Patel JP, Gönen M, Figueroa ME, Fernandez H, Sun Z, Racevskis J, et al. Prognostic Relevance of Integrated Genetic Profiling in Acute Myeloid Leukemia. N Engl J Med. 2012;366:1079-1089. doi: 10. 1056/NEJMoa1112304 PMID: 22417203
    • (2012) N Engl J Med. , vol.366 , pp. 1079-1089
    • Patel, J.P.1    Gönen, M.2    Figueroa, M.E.3    Fernandez, H.4    Sun, Z.5    Racevskis, J.6
  • 16
    • 84859742518 scopus 로고    scopus 로고
    • Molecular genetics of acute myeloid leukemia: Clinical implications and opportunities for integrating genomics into clinical practice
    • Abdel-Wahab. Molecular genetics of acute myeloid leukemia: clinical implications and opportunities for integrating genomics into clinical practice. Hematology. 2012; doi: 10.1179/102453312X13336169155411
    • (2012) Hematology
    • Abdel-Wahab1
  • 17
    • 84878372012 scopus 로고    scopus 로고
    • Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
    • 23634996
    • The Cancer Genome Atlas Research Network. Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia. N EnglJ Med. 2013;368:2059-2074. doi: 10.1056/NEJMoa1301689 PMID: 23634996
    • (2013) N EnglJ Med. , vol.368 , pp. 2059-2074
    • The Cancer Genome Atlas Research Network1
  • 19
    • 0032188805 scopus 로고    scopus 로고
    • The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1, 612 patients entered into the MRC AML 10 trial
    • 9746770
    • Grimwade D, Walker H, Oliver F, Wheatley K, Harrison C, Harrison G, et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1, 612 patients entered into the MRC AML 10 trial. Blood. 1998;92:2322-2333. PMID: 9746770
    • (1998) Blood , vol.92 , pp. 2322-2333
    • Grimwade, D.1    Walker, H.2    Oliver, F.3    Wheatley, K.4    Harrison, C.5    Harrison, G.6
  • 20
    • 77952536841 scopus 로고    scopus 로고
    • IDH1 and IDH2Gene mutations identify novel molecular subsets within de novo cytogenetically normal acute myeloid leukemia: A cancer and leukemia group B study
    • 20368543
    • Marcucci G, Maharry K, Wu YZ, Radmacher MD, Mrozek K, Margeson D, et al. IDH1 and IDH2Gene Mutations Identify Novel Molecular Subsets Within De Novo Cytogenetically Normal Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study. J Clin Oncol. 2010;28:2348-2355. doi: 10.1200/JCO.2009.27.3730 PMID: 20368543
    • (2010) J Clin Oncol. , vol.28 , pp. 2348-2355
    • Marcucci, G.1    Maharry, K.2    Wu, Y.Z.3    Radmacher, M.D.4    Mrozek, K.5    Margeson, D.6
  • 21
    • 84862266735 scopus 로고    scopus 로고
    • TET2 mutations in acute myeloid leukemia (AML): Results from a comprehensive genetic and clinical analysis of the AML study group
    • Gaidzik VI, Paschka P, Späth D, Habdank M, Köhne C-H, Germing U, et al. TET2 mutations in acute myeloid leukemia (AML): results from a comprehensive genetic and clinical analysis of the AML study group. J Clin Oncol Off J Am SocClin Oncol. 2012;30:1350-1357. doi: 10.1200/JCO.2011.39.2886
    • (2012) J Clin Oncol Off J Am SocClin Oncol. , vol.30 , pp. 1350-1357
    • Gaidzik, V.I.1    Paschka, P.2    Späth, D.3    Habdank, M.4    Köhne, C.-H.5    Germing, U.6
  • 22
    • 84873568769 scopus 로고    scopus 로고
    • ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome
    • 23018865
    • Schnittger S, Eder C, Jeromin S, Alpermann T, Fasan A, Grossmann V, et al. ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome. Leukemia. 2013;27:82-91. doi: 10.1038/leu.2012.262 PMID: 23018865
    • (2013) Leukemia , vol.27 , pp. 82-91
    • Schnittger, S.1    Eder, C.2    Jeromin, S.3    Alpermann, T.4    Fasan, A.5    Grossmann, V.6
  • 24
    • 73949090504 scopus 로고    scopus 로고
    • AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: Prognostic implication and interaction with other gene alterations
    • 19808697
    • Tang J-L, Hou H-A, Chen C-Y, Liu C-Y, Chou W-C, Tseng M-H, et al. AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations. Blood. 2009;114:5352-5361. doi: 10.1182/blood-2009-05-223784 PMID: 19808697
    • (2009) Blood , vol.114 , pp. 5352-5361
    • Tang, J.-L.1    Hou, H.-A.2    Chen, C.-Y.3    Liu, C.-Y.4    Chou, W.-C.5    Tseng, M.-H.6
  • 25
    • 79952138375 scopus 로고    scopus 로고
    • Prognostic importance of histone methyltransferase MLL5 expression in acute myeloid leukemia
    • 21205756
    • Damm F, Oberacker T, Thol F, Surdziel E, Wagner K, Chaturvedi A, et al. Prognostic Importance of Histone Methyltransferase MLL5 Expression in Acute Myeloid Leukemia. J Clin Oncol. 2011;29:682-689. doi: 10.1200/JCO.2010.31.1118 PMID: 21205756
    • (2011) J Clin Oncol. , vol.29 , pp. 682-689
    • Damm, F.1    Oberacker, T.2    Thol, F.3    Surdziel, E.4    Wagner, K.5    Chaturvedi, A.6
  • 26
    • 84922341259 scopus 로고    scopus 로고
    • Allogeneic stem-cell transplantation in patients with NPM1-mutated acute myeloid leukemia: Results from a prospective donor versus no-donor analysis of patients after upfront HLA typing within the SAL-AML 2003 trial
    • Röllig C, Bornhäuser M, Kramer M, Thiede C, Ho AD, Krämer A, et al. Allogeneic stem-cell transplantation in patients with NPM1-mutated acute myeloid leukemia: results from a prospective donor versus no-donor analysis of patients after upfront HLA typing within the SAL-AML 2003 trial. J Clin Oncol Off J Am SocClin Oncol. 2015;33:403-410. doi: 10.1200/JCO.2013.54.4973
    • (2015) J Clin Oncol Off J Am SocClin Oncol. , vol.33 , pp. 403-410
    • Röllig, C.1    Bornhäuser, M.2    Kramer, M.3    Thiede, C.4    Ho, A.D.5    Krämer, A.6
  • 28
    • 0036682174 scopus 로고    scopus 로고
    • Prognostic significance of partial tandem duplications of the MLL gene in adult patients 16 to 60 years old with acute myeloid leukemia and normal cytogenetics: A study of the acute myeloid Leukemia Study Group Ulm
    • 12149299
    • Dohner K. Prognostic Significance of Partial Tandem Duplications of the MLL Gene in Adult Patients 16 to 60 Years Old With Acute Myeloid Leukemia and Normal Cytogenetics: A Study of the Acute Myeloid Leukemia Study Group Ulm. J Clin Oncol. 2002;20:3254-3261. doi: 10.1200/JCO.2002.09.088 PMID: 12149299
    • (2002) J Clin Oncol. , vol.20 , pp. 3254-3261
    • Dohner, K.1
  • 29
    • 0031984414 scopus 로고    scopus 로고
    • Rearrangement of ALL1 (MLL) in acute myeloid leukemia with normal cytogenetics
    • 9426057
    • Caligiuri MA, Strout MP, Lawrence D, Arthur DC, Baer MR, Yu F, et al. Rearrangement of ALL1 (MLL) in acute myeloid leukemia with normal cytogenetics. Cancer Res. 1998;58:55-59. PMID: 9426057
    • (1998) Cancer Res. , vol.58 , pp. 55-59
    • Caligiuri, M.A.1    Strout, M.P.2    Lawrence, D.3    Arthur, D.C.4    Baer, M.R.5    Yu, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.