New therapeutic strategies for the treatment of acute lymphoblastic leukaemia

被引:171
作者
Pui, Ching-Hon
Jeha, Sima
机构
[1] St Jude Childrens Res Hosp, Dept Oncol, Memphis, TN 38105 USA
[2] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrd2240
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Although contemporary treatments cure more than 80% of children with acute lymphoblastic leukaemia ( ALL), some patients require intensive treatment and many patients still develop serious acute and late complications owing to the side effects of the treatments. Furthermore, the survival rate for adults with ALL remains below 40%. Therefore, new treatment strategies are needed to improve not only the cure rate but also the quality of life of these patients. Here, we discuss emerging new treatments that might improve the clinical outcome of patients with ALL. These include new formulations of existing chemotherapeutic agents, new antimetabolites and nucleoside analogues, monoclonal antibodies against leukaemia-associated antigens, and molecular therapies that target genetic abnormalities of the leukaemic cells and their affected signalling pathways.
引用
收藏
页码:149 / 165
页数:17
相关论文
共 166 条
[1]   Weekly polyethylene glycol conjugated L-asparaginase compared with biweekly dosing produces superior induction remission rates in childhood relapsed acute lymphoblastic leukemia: a pediatric oncology group study [J].
Abshire, TC ;
Pollock, BH ;
Billett, AL ;
Bradley, P ;
Buchanan, GR .
BLOOD, 2000, 96 (05) :1709-1715
[2]   Synergistic induction of mitochondrial damage and apoptosis in human leukemia cells by flavopiridol and the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) [J].
Almenara, J ;
Rosato, R ;
Grant, S .
LEUKEMIA, 2002, 16 (07) :1331-1343
[3]   Safety and efficacy of gemtuzumab ozogamicin in pediatric patients with advanced CD33+ acute myeloid leukemia [J].
Arceci, RJ ;
Sande, J ;
Lange, B ;
Shannon, K ;
Franklin, J ;
Hutchinson, R ;
Vik, TA ;
Flowers, D ;
Aplenc, R ;
Berger, MS ;
Sherman, ML ;
Smith, FO ;
Bernstein, I ;
Sievers, EL .
BLOOD, 2005, 106 (04) :1183-1188
[4]  
Arguello F, 1998, BLOOD, V91, P2482
[5]   Inhibition of FLT3 in MLL: Validation of a therapeutic target identified by gene expression based classification [J].
Armstrong, SA ;
Kung, AL ;
Mabon, ME ;
Silverman, LB ;
Stam, RW ;
Den Boer, ML ;
Pieters, R ;
Kersey, JH ;
Sallan, SE ;
Fletcher, JA ;
Golub, TR ;
Griffin, JD ;
Korsmeyer, SJ .
CANCER CELL, 2003, 3 (02) :173-183
[6]   Molecular genetics of acute lymphoblastic leukemia [J].
Armstrong, SA ;
Look, AT .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (26) :6306-6315
[7]   MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia [J].
Armstrong, SA ;
Staunton, JE ;
Silverman, LB ;
Pieters, R ;
de Boer, ML ;
Minden, MD ;
Sallan, SE ;
Lander, ES ;
Golub, TR ;
Korsmeyer, SJ .
NATURE GENETICS, 2002, 30 (01) :41-47
[8]   Rapamycin stimulates apoptosis of childhood acute lymphoblastic leukemia cells [J].
Avellino, R ;
Romano, S ;
Parasole, R ;
Bisogni, R ;
Lamberti, A ;
Poggi, V ;
Venuta, S ;
Romano, MF .
BLOOD, 2005, 106 (04) :1400-1406
[9]   2-FLUORO-ATP - A TOXIC METABOLITE OF "9-BETA-D-ARABINOSYL-2-FLUOROADENINE [J].
AVRAMIS, VI ;
PLUNKETT, W .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 113 (01) :35-43
[10]   A randomized comparison of native Escherichia coli asparaginase and polyethylene glycol conjugated asparaginase for treatment of children with newly diagnosed standard-risk acute lymphoblastic leukemia:: a Children's Cancer Group study [J].
Avramis, VI ;
Sencer, S ;
Periclou, AP ;
Sather, H ;
Bostrom, BC ;
Cohen, LJ ;
Ettinger, AG ;
Ettinger, LJ ;
Franklin, J ;
Gaynon, PS ;
Hilden, JM ;
Lange, B ;
Majlessipour, F ;
Mathew, P ;
Needle, M ;
Neglia, J ;
Reaman, G ;
Holcenberg, JS .
BLOOD, 2002, 99 (06) :1986-1994