Progress in the treatment of acute myeloid leukemia

被引:72
作者
Ravandi, Farhad
Burnett, Alan K.
Agura, Edward D.
Kantarjian, Hagop M.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Unit 428, Houston, TX 77030 USA
[2] Cardiff Univ, Dept Haematol, Cardiff, S Glam, Wales
[3] Baylor Univ, Med Ctr, Dallas, TX USA
关键词
acute myeloid leukemia; new agents; risk stratification; therapy;
D O I
10.1002/cncr.23000
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Significant progress in understanding the mechanisms leading to the development of acute myeloid leukemia (AML) has led to the identification of numerous molecular abnormalities that may be responsible for leukemogenesis. Over the same period, large trials have established standard regimens combining cytotoxic agents for the treatment of patients with AML. Current research is attempting to better stratify, patients by identifying risk factors responsible for resistance, and to discern ways for incorporating newer agents with specific and targeted activity into our standard regimens, Herein the recent developments in the diagnosis and treatment of AML are reviewed.
引用
收藏
页码:1900 / 1910
页数:11
相关论文
共 102 条
[1]   Farnesyl transferase inhibitor (Tipifarnib, zarnestra; z) in combination with standard chemotherapy with idarubicin (Ida) and cytarabime (ara-C) for patients (pts) with newly diagnosed acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS). [J].
Alvarez, Ricardo H. ;
Kantarijan, Hagop ;
Garcia-Manero, Guillermo ;
Estrov, Zeev ;
Ravandi-Kashani, Farhad ;
Verstovsek, Srdan ;
Giles, Francis ;
O'Brien, Susan ;
Koller, Charles Asa ;
Faderl, Stefan ;
Thomas, Deborah ;
Wright, John J. ;
Cortes, Jorge .
BLOOD, 2006, 108 (11) :565A-566A
[2]   Comparative outcome of nonmyeloablative and myeloablative allogeneic hematopoietic cell transplantation for patients older than 50 years of age [J].
Alyea, EP ;
Kim, HT ;
Ho, V ;
Cutler, C ;
Gribben, J ;
DeAngelo, DJ ;
Lee, SJ ;
Windawi, S ;
Ritz, J ;
Stone, RM ;
Antin, JH ;
Soiffer, RJ .
BLOOD, 2005, 105 (04) :1810-1814
[3]   Intravenous busulfan in pretransplant chemotherapy: Bioavailability and patient benefit [J].
Andersson, BS ;
Kashyap, A ;
Couriel, D ;
Madden, T ;
Thall, PF ;
Fernandez, H ;
Vaughan, WP ;
Jones, R ;
Wingard, JR ;
Blume, KG ;
Champlin, RE .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2003, 9 (11) :722-724
[4]   Age and acute myeloid leukemia [J].
Appelbaum, FR ;
Gundacker, H ;
Head, DR ;
Slovak, ML ;
Willman, CL ;
Godwin, JE ;
Anderson, JE ;
Petersdorf, SH .
BLOOD, 2006, 107 (09) :3481-3485
[5]   PROSPECTIVE GENETICALLY RANDOMIZED COMPARISON BETWEEN INTENSIVE POSTINDUCTION CHEMOTHERAPY AND BONE-MARROW TRANSPLANTATION IN ADULTS WITH NEWLY-DIAGNOSED ACUTE MYELOID-LEUKEMIA [J].
ARCHIMBAUD, E ;
THOMAS, X ;
MICHALLET, M ;
JAUBERT, J ;
TRONCY, J ;
GUYOTAT, D ;
FIERE, D .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (02) :262-267
[6]   Implications of NRAS mutations in AML:: a study of 2502 patients [J].
Bacher, Ulrike ;
Haferlach, Torsten ;
Schoch, Claudia ;
Kern, Wolfgang ;
Schnittger, Susanne .
BLOOD, 2006, 107 (10) :3847-3853
[7]   BAALC expression and FLT3 internal tandem duplication mutations in acute myeloid leukemia patients with normal cytogenetics:: Prognostic implications [J].
Baldus, CD ;
Thiede, C ;
Soucek, S ;
Bloomfield, CD ;
Thiel, E ;
Ehninger, G .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (05) :790-797
[8]   BAALC expression predicts clinical outcome of de novo acute myeloid leukemia patients with normal cytogenetics:: a Cancer and Leukemia Group B Study [J].
Baldus, CD ;
Tanner, SM ;
Ruppert, AS ;
Whitman, SP ;
Archer, KJ ;
Marcucci, G ;
Caligiuri, MA ;
Carroll, AJ ;
Vardiman, JW ;
Powell, BL ;
Allen, SL ;
Moore, JO ;
Larson, RA ;
Kolitz, JE ;
de la Chapelle, A ;
Bloomfield, CD .
BLOOD, 2003, 102 (05) :1613-1618
[9]   High levels of Wilms' tumor gene (wt1) mRNA in acute myeloid leukemias are associated with a worse long-term outcome [J].
Bergmann, L ;
Miething, C ;
Maurer, U ;
Brieger, J ;
Karakas, T ;
Weidmann, E ;
Hoelzer, D .
BLOOD, 1997, 90 (03) :1217-1225
[10]  
BERMAN E, 1991, BLOOD, V77, P1666