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Volumn 27, Issue 11, 2014, Pages 1438-1446

Detection of minimal residual disease in NPM1-mutated acute myeloid leukemia by next-generation sequencing

Author keywords

acute myeloid leukemia; minimal residual disease; next generation sequencing; NPM1; prognosis; relapse; tumor heterogeneity

Indexed keywords

NUCLEOPHOSMIN; NUCLEAR PROTEIN; TUMOR MARKER;

EID: 84926148720     PISSN: 08933952     EISSN: 15300285     Source Type: Journal    
DOI: 10.1038/modpathol.2014.57     Document Type: Article
Times cited : (49)

References (40)
  • 1
    • 57549101876 scopus 로고    scopus 로고
    • Quantitative monitoring of NPM1 mutations provides a valid minimal residual disease parameter following allo-geneic stem cell transplantation
    • Bacher U, Badbaran A, Fehse B, et al. Quantitative monitoring of NPM1 mutations provides a valid minimal residual disease parameter following allo-geneic stem cell transplantation. Exp Hematol 2009; 37:135-1342.
    • (2009) Exp Hematol , vol.37 , pp. 135-1342
    • Bacher, U.1    Badbaran, A.2    Fehse, B.3
  • 2
    • 84886509637 scopus 로고    scopus 로고
    • Significance of minimal residual disease before myeloablative allo-geneic hematopoietic cell transplantation for AML in first and second complete remission
    • Walter RB, Buckley SA, Pagel JM, et al. Significance of minimal residual disease before myeloablative allo-geneic hematopoietic cell transplantation for AML in first and second complete remission. Blood 2013; 122:1813-1821.
    • (2013) Blood , vol.122 , pp. 1813-1821
    • Walter, R.B.1    Buckley, S.A.2    Pagel, J.M.3
  • 3
    • 79952757082 scopus 로고    scopus 로고
    • Impact of pretransplantation minimal residual disease, as detected by multiparametric flow cytometry, on outcome of myeloablative hematopoietic cell transplantation for acute myeloid leukemia
    • Walter RB, Gooley TA, Wood BL, et al. Impact of pretransplantation minimal residual disease, as detected by multiparametric flow cytometry, on outcome of myeloablative hematopoietic cell transplantation for acute myeloid leukemia. J Clin Oncol 2011;29: 1190-1197.
    • (2011) J Clin Oncol , vol.29 , pp. 1190-1197
    • Walter, R.B.1    Gooley, T.A.2    Wood, B.L.3
  • 4
    • 70349579540 scopus 로고    scopus 로고
    • Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML
    • Schnittger S, Kern W, Tschulik C, et al. Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML. Blood 2009;114:2220-2231.
    • (2009) Blood , vol.114 , pp. 2220-2231
    • Schnittger, S.1    Kern, W.2    Tschulik, C.3
  • 5
    • 5444223232 scopus 로고    scopus 로고
    • Determination of relapse risk based on assessment of minimal residual disease during complete remission by multiparameter flow cytometry in unselected patients with acute myeloid leukemia
    • Kern W, Voskova D, Schoch C, et al. Determination of relapse risk based on assessment of minimal residual disease during complete remission by multiparameter flow cytometry in unselected patients with acute myeloid leukemia. Blood 2004;104:3078-3085.
    • (2004) Blood , vol.104 , pp. 3078-3085
    • Kern, W.1    Voskova, D.2    Schoch, C.3
  • 6
    • 84883243212 scopus 로고    scopus 로고
    • Flow cytometric monitoring of residual disease in acute leukemia
    • Wood BL. Flow cytometric monitoring of residual disease in acute leukemia. Methods Mol Biol 2013; 999:123-136.
    • (2013) Methods Mol Biol , vol.999 , pp. 123-136
    • Wood, B.L.1
  • 7
    • 7744244145 scopus 로고    scopus 로고
    • Stability of leukemia-associated aberrant immunophenotypes in patients with acute myeloid leukemia between diagnosis and relapse: Comparison with cytomorpho-logic, cytogenetic, and molecular genetic findings
    • Voskova D, Schoch C, Schnittger S, et al. Stability of leukemia-associated aberrant immunophenotypes in patients with acute myeloid leukemia between diagnosis and relapse: comparison with cytomorpho-logic, cytogenetic, and molecular genetic findings. Cytometry B 2004;62:25-38.
    • (2004) Cytometry B , vol.62 , pp. 25-38
    • Voskova, D.1    Schoch, C.2    Schnittger, S.3
  • 8
    • 79251556241 scopus 로고    scopus 로고
    • Acute myeloid leukemia with mutated nucleophosmin (NPM1): Is it a distinct entity?
    • Falini B, Martelli MP, Bolli N, et al. Acute myeloid leukemia with mutated nucleophosmin (NPM1): is it a distinct entity? Blood 2011;117:1109-1120.
    • (2011) Blood , vol.117 , pp. 1109-1120
    • Falini, B.1    Martelli, M.P.2    Bolli, N.3
  • 9
    • 19944427850 scopus 로고    scopus 로고
    • Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
    • Falini B, Mecucci C, Tiacci E, et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med 2005;352:254-266.
    • (2005) N Engl J Med , vol.352 , pp. 254-266
    • Falini, B.1    Mecucci, C.2    Tiacci, E.3
  • 10
    • 84890409823 scopus 로고    scopus 로고
    • Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens
    • Pritchard CC, Salipante SJ, Koehler K, et al. Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens. J Mol Diagn 2014;16:56-67.
    • (2014) J Mol Diagn , vol.16 , pp. 56-67
    • Pritchard, C.C.1    Salipante, S.J.2    Koehler, K.3
  • 11
    • 84860675045 scopus 로고    scopus 로고
    • Next-generation sequencing for minimal residual disease monitoring in acute myeloid leukemia patients with FLT3-ITD or NPM1 mutations
    • Thol F, Kolking B, Damm F, et al. Next-generation sequencing for minimal residual disease monitoring in acute myeloid leukemia patients with FLT3-ITD or NPM1 mutations. Genes Chromosomes Cancer 2012; 51:689-695.
    • (2012) Genes Chromosomes Cancer , vol.51 , pp. 689-695
    • Thol, F.1    Kolking, B.2    Damm, F.3
  • 12
    • 84861120541 scopus 로고    scopus 로고
    • High-throughput sequencing detects minimal residual disease in acute T lymphoblastic leukemia
    • Wu D, Sherwood A, Fromm JR, et al. High-throughput sequencing detects minimal residual disease in acute T lymphoblastic leukemia. Sci Transl Med 2012;4: 134ra63.
    • (2012) Sci Transl Med , vol.4 , pp. 134ra63
    • Wu, D.1    Sherwood, A.2    Fromm, J.R.3
  • 13
    • 84871525322 scopus 로고    scopus 로고
    • Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia
    • Faham M, Zheng J, Moorhead M, et al. Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia. Blood 2012;120: 5173-5180.
    • (2012) Blood , vol.120 , pp. 5173-5180
    • Faham, M.1    Zheng, J.2    Moorhead, M.3
  • 15
    • 33646710679 scopus 로고    scopus 로고
    • 9-color and 10-color flow cytometry in the clinical laboratory
    • Wood B. 9-color and 10-color flow cytometry in the clinical laboratory. Arch Pathol Lab Med 2006;130: 680-690.
    • (2006) Arch Pathol Lab Med , vol.130 , pp. 680-690
    • Wood, B.1
  • 16
    • 84863981120 scopus 로고    scopus 로고
    • Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
    • Caporaso JG, Lauber CL, Walters WA, et al. Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J 2012;6: 1621-1624.
    • (2012) ISME J , vol.6 , pp. 1621-1624
    • Caporaso, J.G.1    Lauber, C.L.2    Walters, W.A.3
  • 18
    • 77949587649 scopus 로고    scopus 로고
    • Fast and accurate long-read alignment with Burrows-Wheeler transform
    • Li H, Durbin R. Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 2010;26:589-595.
    • (2010) Bioinformatics , vol.26 , pp. 589-595
    • Li, H.1    Durbin, R.2
  • 19
    • 84877108149 scopus 로고    scopus 로고
    • Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation
    • Hiatt JB, Pritchard CC, Salipante SJ, O'Roak BJ, Shendure J. Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation. Genome Res 2013;23:843-854.
    • (2013) Genome Res , vol.23 , pp. 843-854
    • Hiatt, J.B.1    Pritchard, C.C.2    Salipante, S.J.3    O'Roak, B.J.4    Shendure, J.5
  • 20
    • 84863229597 scopus 로고    scopus 로고
    • VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
    • Koboldt DC, Zhang Q, Larson DE, et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res 2012; 22:568-576.
    • (2012) Genome Res , vol.22 , pp. 568-576
    • Koboldt, D.C.1    Zhang, Q.2    De, L.3
  • 21
    • 27144501134 scopus 로고    scopus 로고
    • Cell line OCI/AML3 bears exon-12 NPM gene mutation-A and cytoplasmic expression of nucleophosmin
    • Quentmeier H, Martelli MP, Dirks WG, et al. Cell line OCI/AML3 bears exon-12 NPM gene mutation-A and cytoplasmic expression of nucleophosmin. Leukemia 2005;19:1760-1767.
    • (2005) Leukemia , vol.19 , pp. 1760-1767
    • Quentmeier, H.1    Martelli, M.P.2    Dirks, W.G.3
  • 22
    • 79960127726 scopus 로고    scopus 로고
    • Monitoring of minimal residual disease in NPM1-mutated acute myeloid leukemia: A study from the German-Austrian acute myeloid leukemia study group
    • Kronke J, Schlenk RF, Jensen KO, 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 Clin Oncol 2011;29:2709-2716.
    • (2011) J Clin Oncol , vol.29 , pp. 2709-2716
    • Kronke, J.1    Schlenk, R.F.2    Jensen, K.O.3
  • 23
    • 24144494881 scopus 로고    scopus 로고
    • Clinical characteristics and prognostic implications of NPM1 mutations in acute myeloid leukemia
    • Suzuki T, Kiyoi H, Ozeki K, et al. Clinical characteristics and prognostic implications of NPM1 mutations in acute myeloid leukemia. Blood 2005;106: 2854-2861.
    • (2005) Blood , vol.106 , pp. 2854-2861
    • Suzuki, T.1    Kiyoi, H.2    Ozeki, K.3
  • 24
    • 84883730914 scopus 로고    scopus 로고
    • Clonal evolution in relapsed NPM1-mutated acute myeloid leukemia
    • Kronke J, Bullinger L, Teleanu V, et al. Clonal evolution in relapsed NPM1-mutated acute myeloid leukemia. Blood 2013;122:100-108.
    • (2013) Blood , vol.122 , pp. 100-108
    • Kronke, J.1    Bullinger, L.2    Teleanu, V.3
  • 25
    • 77956794315 scopus 로고    scopus 로고
    • Performance and clinical evaluation of a sensitive multiplex assay for the rapid detection of common NPM1 mutations
    • Hafez M, Ye F, Jackson K, et al. Performance and clinical evaluation of a sensitive multiplex assay for the rapid detection of common NPM1 mutations. J Mol Diagn 2010;12:629-635.
    • (2010) J Mol Diagn , vol.12 , pp. 629-635
    • Hafez, M.1    Ye, F.2    Jackson, K.3
  • 26
    • 84883677161 scopus 로고    scopus 로고
    • The level of residual disease based on mutant NPM1 is an independent prognostic factor for relapse and survival in AML
    • Shayegi N, Kramer M, Bornhauser M, et al. The level of residual disease based on mutant NPM1 is an independent prognostic factor for relapse and survival in AML. Blood 2013;122:83-92.
    • (2013) Blood , vol.122 , pp. 83-92
    • Shayegi, N.1    Kramer, M.2    Bornhauser, M.3
  • 27
    • 84879350221 scopus 로고    scopus 로고
    • Minimal residual disease in acute myeloid leukemia: Coming of age
    • Paietta E. Minimal residual disease in acute myeloid leukemia: coming of age. Hematology Am Soc Hematol Educ Program 2012;2012:35-42.
    • (2012) Hematology Am Soc Hematol Educ Program , vol.2012 , pp. 35-42
    • Paietta, E.1
  • 28
    • 84855838173 scopus 로고    scopus 로고
    • Prognostic and therapeutic implications of minimal residual disease detection in acute myeloid leukemia
    • Buccisano F, Maurillo L, Del Principe MI, et al. Prognostic and therapeutic implications of minimal residual disease detection in acute myeloid leukemia. Blood 2011;119:332-341.
    • (2011) Blood , vol.119 , pp. 332-341
    • Buccisano, F.1    Maurillo, L.2    Del Principe, M.I.3
  • 30
    • 77958468721 scopus 로고    scopus 로고
    • Assessment of minimal residual disease in acute myeloid leukemia
    • Grimwade D, Vyas P, Freeman S. Assessment of minimal residual disease in acute myeloid leukemia. Curr Opin Oncol 2010;22:656-663.
    • (2010) Curr Opin Oncol , vol.22 , pp. 656-663
    • Grimwade, D.1    Vyas, P.2    Freeman, S.3
  • 31
    • 48749123479 scopus 로고    scopus 로고
    • Development of minimal residual disease-directed therapy in acute myeloid leukemia
    • Freeman SD, Jovanovic JV, Grimwade D. Development of minimal residual disease-directed therapy in acute myeloid leukemia. Semin Oncol 2008;35:388-400.
    • (2008) Semin Oncol , vol.35 , pp. 388-400
    • Freeman, S.D.1    Jovanovic, J.V.2    Grimwade, D.3
  • 32
    • 10744230697 scopus 로고    scopus 로고
    • A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes
    • Ley TJ, Minx PJ, Walter MJ, et al. A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes. Proc Natl Acad Sci USA 2003;100: 14275-14280.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 14275-14280
    • Ley, T.J.1    Minx, P.J.2    Walter, M.J.3
  • 33
    • 84883743375 scopus 로고    scopus 로고
    • Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture
    • Conte N, Varela I, Grove C, et al. Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture. Leukemia 2013;27:1820-1825.
    • (2013) Leukemia , vol.27 , pp. 1820-1825
    • Conte, N.1    Varela, I.2    Grove, C.3
  • 34
    • 70149093912 scopus 로고    scopus 로고
    • Recurring mutations found by sequencing an acute myeloid leukemia genome
    • Mardis ER, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 2009;361:1058-1066.
    • (2009) N Engl J Med , vol.361 , pp. 1058-1066
    • Mardis, E.R.1    Ding, L.2    Dooling, D.J.3
  • 35
    • 84864255882 scopus 로고    scopus 로고
    • The origin and evolution of mutations in acute myeloid leukemia
    • Welch JS, Ley TJ, Link DC, et al. The origin and evolution of mutations in acute myeloid leukemia. Cell 2012;150:264-278.
    • (2012) Cell , vol.150 , pp. 264-278
    • Welch, J.S.1    Ley, T.J.2    Link, D.C.3
  • 36
    • 84862776906 scopus 로고    scopus 로고
    • Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
    • Ding L, Ley TJ, Larson DE, et al. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature 2012;481:506-510.
    • (2012) Nature , vol.481 , pp. 506-510
    • Ding, L.1    Ley, T.J.2    De, L.3
  • 37
    • 84878372012 scopus 로고    scopus 로고
    • Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
    • Network TCGAR. Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med 2013;368:2059-2074.
    • (2013) N Engl J Med , vol.368 , pp. 2059-2074
  • 38
    • 83655211930 scopus 로고    scopus 로고
    • Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing
    • Harismendy O, Schwab RB, Bao L, et al. Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing. Genome Biol 2011;12:R124.
    • (2011) Genome Biol , vol.12 , pp. R124
    • Harismendy, O.1    Schwab, R.B.2    Bao, L.3
  • 39
    • 84891589611 scopus 로고    scopus 로고
    • Clonal heterogeneity as detected by metaphase karyotyping is an indicator of poor prognosis in acute myeloid leukemia
    • Bochtler T, Stolzel F, Heilig CE, et al. Clonal heterogeneity as detected by metaphase karyotyping is an indicator of poor prognosis in acute myeloid leukemia. J Clin Oncol 2013;31:3898-3905.
    • (2013) J Clin Oncol , vol.31 , pp. 3898-3905
    • Bochtler, T.1    Stolzel, F.2    Heilig, C.E.3
  • 40
    • 84907845842 scopus 로고    scopus 로고
    • Evaluation of different NPM1 mutations in AML patients according to clinical, cytogenetic and molecular features and impact on outcome
    • Alpermann T, Haferlach C, Dicker F, et al. Evaluation of different NPM1 mutations in AML patients according to clinical, cytogenetic and molecular features and impact on outcome. Blood 2013;122:51.
    • (2013) Blood , vol.122 , pp. 51
    • Alpermann, T.1    Haferlach, C.2    Dicker, F.3


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