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ASH CAP Initial Workup of Acute Leukemia Included References for Data Extraction

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ASH CAP Initial Workup of Acute Leukemia Included References for Data Extraction 1. Busse, N. Gokbuget, J. M. Siehl, D. Hoelzer, S. Schwartz, A. Rietz, E. Thiel and U. Keilholz. Wilms' tumor gene 1 (WT1)
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ASH CAP Initial Workup of Acute Leukemia Included References for Data Extraction 1. Busse, N. Gokbuget, J. M. Siehl, D. Hoelzer, S. Schwartz, A. Rietz, E. Thiel and U. Keilholz. Wilms' tumor gene 1 (WT1) expression in subtypes of acute lymphoblastic leukemia (ALL) of adults and impact on clinical outcome. Annals of Hematology : Dufour, F. Schneider, K. H. Metzeler, E. Hoster, S. Schneider, E. Zellmeier, T. Benthaus, M. C. Sauerland, W. E. Berdel, T. Buchner, B. Wormann, J. Braess, W. Hiddemann, S. K. Bohlander and K. Spiekermann. Acute myeloid leukemia with biallelic CEBPA gene mutations and normal karyotype represents a distinct genetic entity associated with a favorable clinical outcome. J Clin Oncol : J. Mead, D. C. Linch, R. K. Hills, K. Wheatley, A. K. Burnett and R. E. Gale. FLT3 tyrosine kinase domain mutations are biologically distinct from and have a significantly more favorable prognosis than FLT3 internal tandem duplications in patients with acute myeloid leukemia. Blood : Jaworska-Posadzy, J. Styczynski, M. Kubicka, R. Debski, B. Rafinska-Kurylo, B. Kolodziej, M. Pogorzala and M. Wysocki. Prognostic value of persistent peripheral blood and bone marrow lymphoblasts on day 15 of therapy in childhood acute lymphoblastic leukemia as detected by flow cytometry. Anticancer Research : Kuhnl, N. Gokbuget, A. Stroux, T. Burmeister, M. Neumann, S. Heesch, T. Haferlach, D. Hoelzer, W. K. Hofmann, E. Thiel and C. D. Baldus. High BAALC expression predicts chemoresistance in adult B-precursor acute lymphoblastic leukemia. Blood : Neubauer, K. Maharry, K. Mrozek, C. Thiede, G. Marcucci, P. Paschka, R. J. Mayer, R. A. Larson, E. T. Liu and C. D. Bloomfield. Patients with acute myeloid leukemia and RAS mutations benefit most from postremission high-dose cytarabine: a Cancer and Leukemia Group B study. J Clin Oncol : Ongaro, M. De Mattei, M. G. Della Porta, G. Rigolin, C. Ambrosio, F. Di Raimondo, A. Pellati, F. F. Masieri, A. Caruso, L. Catozzi and D. Gemmati. 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Pautas, O. Reman, X. Thomas, C. Gardin, C. Terre, S. Castaigne, C. Preudhomme and H. Dombret. The favorable impact of CEBPA mutations in patients with acute myeloid leukemia is only observed in the absence of associated cytogenetic abnormalities and FLT3 internal duplication. Blood : Renneville, N. Boissel, O. Nibourel, C. Berthon, N. Helevaut, C. Gardin, J. M. Cayuela, S. Hayette, O. Reman, N. Contentin, D. Bordessoule, C. Pautas, S. d. Botton, T. d. Revel, C. Terre, P. Fenaux, X. Thomas, S. Castaigne, H. Dombret and C. Preudhomme. Prognostic significance of DNA methyltransferase 3A mutations in cytogenetically normal acute myeloid leukemia: a study by the Acute Leukemia French Association. Leukemia : Shimada, T. Taki, K. Tabuchi, T. Taketani, R. Hanada, A. Tawa, M. Tsuchida, K. Horibe, I. Tsukimoto and Y. Hayashi. Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study Group. 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Prognostic impact of monosomal karyotype in young adult and elderly acute myeloid leukemia: the Southwest Oncology Group (SWOG) experience. Blood : Chapuy, R. Koch, U. Radunski, S. Corsham, N. Cheong, N. Inagaki, N. Ban, D. Wenzel, D. Reinhardt, A. Zapf, S. Schweyer, F. Kosari, W. Klapper, L. Truemper and G. G. Wulf. Intracellular ABC transporter A3 confers multidrug resistance in leukemia cells by lysosomal drug sequestration. Leukemia : Falini, K. Macijewski, T. Weiss, U. Bacher, S. Schnittger, W. Kern, A. Kohlmann, H.-U. Klein, M. Vignetti, A. Piciocchi, P. Fazi, M. P. Martelli, A. Vitale, S. Pileri, M. Miesner, A. Santucci, C. Haferlach, F. Mandelli and T. Haferlach. Multilineage dysplasia has no impact on biologic, clinicopathologic, and prognostic features of AML with mutated nucleophosmin (NPM1).[Erratum appears in Blood Aug 12;116(6):1017]. Blood : J. Lange, F. O. Smith, J. Feusner, D. R. Barnard, P. Dinndorf, S. Feig, N. A. Heerema, C. Arndt, R. J. Arceci, N. Seibel, M. Weiman, K. Dusenbery, K. Shannon, S. Luna-Fineman, R. B. Gerbing and T. A. Alonzo. Outcomes in CCG-2961, a children's oncology group phase 3 trial for untreated pediatric acute myeloid leukemia: a report from the children's oncology group. Blood : Jiao, C. F. Wu, Y. Liang, H. M. Chen, S. M. Xiong, B. Chen, J. Y. Shi, Y. Y. Wang, J. H. Wang, Y. Chen, J. M. Li, L. J. Gu, J. Y. Tang, Z. X. Shen, B. W. Gu, W. L. Zhao, Z. Chen and S. J. Chen. AML1-ETO9a is correlated with C-KIT overexpression/mutations and indicates poor disease outcome in t(8;21) acute myeloid leukemia-m2. Leukemia : Patel, L. Rai, G. Buck, S. M. Richards, Y. Mortuza, W. Mitchell, G. Gerrard, A. V. Moorman, V. Duke, A. V. Hoffbrand, A. K. Fielding, A. H. Goldstone and L. Foroni. Minimal residual disease is a significant predictor of treatment failure in non T-lineage adult acute lymphoblastic leukaemia: final results of the international trial UKALL XII/ECOG2993. Br J Haematol : van der Holt, D. A. Breems, H. Berna Beverloo, E. van den Berg, A. K. Burnett, P. Sonneveld and B. Lowenberg. Various distinctive cytogenetic abnormalities in patients with acute myeloid leukaemia aged 60 years and older express adverse prognostic value: results from a prospective clinical trial. British Journal of Haematology : A. Scrideli, J. G. Assumpcao, M. A. Ganazza, M. Araujo, S. R. Toledo, M. L. Lee, E. Delbuono, A. S. Petrilli, R. P. Queiroz, A. Biondi, M. B. Viana, J. A. Yunes, S. R. Brandalise and L. G. Tone. A simplified minimal residual disease polymerase chain reaction method at early treatment points can stratify children with acute lymphoblastic leukemia into good and poor outcome groups. Haematologica : A. Scrideli, M. A. A. Cortez, J. A. Yunes, R. G. d. P. Queiroz, E. T. Valera, J. F. da Mata, S. R. C. Toledo, P. Pavoni-Ferreira, M. L. d. M. Lee, A. S. Petrilli, S. R. Brandalise and L. G. 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Long-term results of St Jude Total Therapy Studies 11, 12, 13A, 13B, and 14 for childhood acute lymphoblastic leukemia. Leukemia : Haferlach, C. Mecucci, S. Schnittger, A. Kohlmann, M. Mancini, A. Cuneo, N. Testoni, G. Rege-Cambrin, A. Santucci, M. Vignetti, P. Fazi, M. P. Martelli, T. Haferlach and B. Falini. AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features. Blood : J. Harrison, R. K. Hills, A. V. Moorman, D. J. Grimwade, I. Hann, D. K. Webb, K. Wheatley, S. S. de Graaf, E. van den Berg, A. K. Burnett and B. E. Gibson. Cytogenetics of childhood acute myeloid leukemia: United Kingdom Medical Research Council Treatment trials AML 10 and 12. J Clin Oncol : Kox, M. Zimmermann, M. Stanulla, S. Leible, M. Schrappe, W. D. Ludwig, R. Koehler, G. Tolle, O. R. Bandapalli, S. Breit, M. U. Muckenthaler and A. E. Kulozik. 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