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高危急性髓系白血病诊疗进展:第55届美国血液学会年会报道 被引量:3

Diagnostic and therapeutic advances of high risk acute myeloid leukemia: reports from the 55th ASH annual meeting
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摘要 近年来,在急性髓系白血病(AML)中发现了多种染色体异常和基因突变并确定了其预后价值.提高对白血病生物学特点的认识有助于对其进行准确的诊断、预后分层以及监测微小残留病变,有利于开发靶向治疗药物和提高预后.文章就2013年美国血液学会年会上关于高危AML的染色体和基因突变特点以及临床试验中的新药研究现状进行综述. Acute myeloid leukemia (AML) is a group of heterogeneous diseases with diverse genetic abnormalities,variable responsiveness to therapy and prognosis.In recent years,a lot of information has become available regarding chromosome and gene mutations that occur in AML and their influence on prognosis.Improvements in the understanding of molecular biology of AML are critical for accurate diagnosis.risk stratification,monitoring of minimal residual disease and provides opportunities to develop targeted therapies and improve the clinical outcome.This article reviewed chromosome abnormalities and characteristic gene mutations,and discussed their clinical signiflcances and presented new drugs in clinical trials presented in the 55th ASH annual meeting.
出处 《白血病.淋巴瘤》 CAS 2014年第3期129-132,136,共5页 Journal of Leukemia & Lymphoma
关键词 白血病 急性 髓系 细胞遗传学 分子遗传学 危险分层 诊断 治疗 美国血液学会年会 Leukemia,acute,myeloid Molecular genetics Cytogenetics Risk stratification Diagnosis Therapy ASH annual meeting
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  • 1Schiller GJ. High-risk acute myelogenous leukemia: treatment today and tomorrow[J]. Blood (ASH Annual Meeting Abstracts), 2013, 1:201-208.
  • 2Byrd JC, K Mr6zek, Dodge RK, et al. Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patienls with de novo acute myetoid leukemia: results from Cancer and Leukemia Group B (CALGB 846 l)[J]. Blood, 2002, 100: 4325-4336.
  • 3Grimwade D, Hills RK, Moorman AV, et al. Refinement of cytogenetie classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients trealed in the United Kingdom Medical Research Council Trials[J]. Blood, 2010, 116: 354-365.
  • 4Frtihling S, Sehlenk RF, Kayser S, et at. Cytogenetics and age are major determinants of outcome in intensively treated acute myeloid leukemia patients older than 60 years: results from AMLSG trial AML HD98-B[J]. Blood, 2006, 108: 3280-3288.
  • 5Speck NA, Gilliland DG. Core-binding fa~ tors in haematopoiesis and Icukacmia[J]. Nat Rev Cancer, 2002, 2: 502-513.
  • 6Okuda T, van Deursen J, Hiebert SW, et at. The target ofmuhiple chromosomal translocations in human leukemia, is essential for nornM fetal liver hematnpoiesis[J]. Cell, 1996, 84:321-330.
  • 7Wang Q, Stacy T, Miller JD, et at. The CBFbeta subunit is essential for CBFalpha2 (AMLI)flmction in vivo[J]. Cell, 1996, 87: 697-708.
  • 8Erickson P, Gao J, Chang KS, et at. Identification of breakpnints in t(8; 21) acute myelogenous leukemia and isolation of a fusion transcript, AML1/ETO, with similarity to Drosophila segmentation gene, nmt[J]. Blood, 1992, 80: 1825-1831.
  • 9Liu P, Tarlc SA, Hajra A, ct al. Fusion between transcription faftor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia[J]. Sci, 1993, 261: 1041-1044.
  • 10ShurtleffSA, Meyers S, Hieberi SW, et at. Heterogeneity in CBF beta/MYHI 1 fusion messages encoded by the inv(l 6)(pl 3q22) and the t(16; 16)(p 13;q22) in acute myelogenous leukemia[J]. Blood, 1995, 85: 3695-3703.

同被引文献21

  • 1向伟,肖晖,肖慕然,宋燕燕.急性髓细胞白血病伴核仁磷酸蛋白突变1例病例报告并文献复习[J].内科急危重症杂志,2020,0(1):69-72. 被引量:1
  • 2李玲,温丙昭,王蕊,迪丽娜孜,钟笛,郭新红,王蕾,郝建萍,陈王容,马力.急性髓系白血病细胞表面同时表现淋系抗原的临床及免疫学分析[J].白血病.淋巴瘤,2005,14(1):14-16. 被引量:4
  • 3Milligan DW,Grimwade D,CullisJ O,侯理.成人急性髓系白血病治疗指南[J].国际输血及血液学杂志,2006,29(2):167-177. 被引量:7
  • 4张之南.血液病诊断及疗效标准[M].3版.北京:科学出版社,2008:1.
  • 5Speck NA, Gilliland DG. Core-binding factors in haematopoiesis and leukaemia [ J ]. Nat Rev Cancer, 2002, 2( 7 ) : 502-513.
  • 6Okuda T, van Deursen J, Hieben SW, et al. AML1, the target of multiple chromosomal translocations in human leukemia,is essential for normal fetal liver hematopoiesis [ J ]. Cell, 1996, 84 ( 2 ) : 321- 330.
  • 7Wang Q, Staey T, Miller JD, et al. The CBF beta subunit is essential for CBFalpha2 ( AML1 )function in vivo [ J ]. Cell, 1996, 87 ( 4 ) : 697-708.
  • 8Eriekson P, Gao J, Chang KS, et al. Identification of breakpoints in t ( 8 ; 21 ) acute myelogenous leukemia and isolation of a fusion transcript,AML1 / ETO,with similarity to Drosophila segmentation gene,runt [ J ]. Blood, 1992, 80( 7 ) : 1825-1831.
  • 9Liu P, Tarl SA, Hajra A, et al. Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia[ J ]. Science, 1993, 261 ( 5124 ) : 1041-1044.
  • 10Shurtleff SA, Meyers S, Hiebert SW, et al. Heterogeneity in CBF beta/MYHU fusion messages encoded by the inv ( 16 ) ( p13q22 ) and the t ( 16:16 ) ( p 13 ; q22 ) in acute myelogenous leukemia [ J ]. Blood, 1995, 85: 3695-3703.

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