Imatinib mesylate in the treatment of chronic myeloid leukaemia

被引:34
作者
Druker, BJ [1 ]
机构
[1] Oregon Hlth & Sci Univ, Inst Canc, Howard Hughes Med Inst, JELD WEN,Chair Leukemia Res, Portland, OR 97239 USA
关键词
Bcr-abl; chronic myeloid leukaemia; imatinib mesylate; tyrosine kinase inhibitor;
D O I
10.1517/14656566.4.6.963
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Imatinib mesylate (Gleevec(TM), Glivec(R), formerly STI571; Novartis Pharmaceuticals) is an inhibitor of the Bcr-abl tyrosine kinase that is central to the pathogenesis of chronic myeloid leukaemia (CML). The remarkable results of imatinib mesylate in clinical trials have rapidly and profoundly changed the management of patients with CML. This article will review the development of this molecularly targeted agent. The clinical trials with imatinib mesylate will be summarised along with the pharmacology of this agent. Despite the impressive responses seen in chronic-phase patients, numerous questions remain. For example, how durable will responses to imatinib mesylate be and is it necessary or possible to improve upon these results? Ongoing efforts to address these issues will be discussed.
引用
收藏
页码:963 / 971
页数:9
相关论文
共 58 条
[21]  
GAMBACORTIPASSE.CB, LANCET ONCOL, V4, P75
[22]   Inhibition of the ABL kinase activity blocks the proliferation of BCR/ABL(+) leukemic cells and induces apoptosis [J].
GambacortiPasserini, C ;
leCoutre, P ;
Mologni, L ;
Fanelli, M ;
Bertazzoli, C ;
Marchesi, E ;
DiNicola, M ;
Biondi, A ;
Corneo, GM ;
Belotti, D ;
Pogliani, E ;
Lydon, NB .
BLOOD CELLS MOLECULES AND DISEASES, 1997, 23 (19) :380-394
[23]  
Gardembas M, 2002, BLOOD, V100, p95A
[24]   Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification [J].
Gorre, ME ;
Mohammed, M ;
Ellwood, K ;
Hsu, N ;
Paquette, R ;
Rao, PN ;
Sawyers, CL .
SCIENCE, 2001, 293 (5531) :876-880
[25]   Primitive, quiescent, Philadelphia-positive stem cells from patients with chronic myeloid leukemia are insensitive to STI571 in vitro [J].
Graham, SM ;
Jorgensen, HG ;
Allan, E ;
Pearson, C ;
Alcorn, MJ ;
Richmond, L ;
Holyoake, TL .
BLOOD, 2002, 99 (01) :319-325
[26]   Direct binding of CRKL to BCR-ABL is not required for BCR-ABL transformation [J].
Heaney, C ;
Kolibaba, K ;
Bhat, A ;
Oda, T ;
Ohno, S ;
Fanning, S ;
Druker, BJ .
BLOOD, 1997, 89 (01) :297-306
[27]   ACUTE-LEUKEMIA IN BCR/ABL TRANSGENIC MICE [J].
HEISTERKAMP, N ;
JENSTER, G ;
TENHOEVE, J ;
ZOVICH, D ;
PATTENGALE, PK ;
GROFFEN, J .
NATURE, 1990, 344 (6263) :251-253
[28]   UNIQUE FUSION OF BCR AND C-ABL GENES IN PHILADELPHIA-CHROMOSOME POSITIVE ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
HERMANS, A ;
HEISTERKAMP, N ;
VONLINDERN, M ;
VANBAAL, S ;
MEIJER, D ;
VANDERPLAS, D ;
WIEDEMANN, LM ;
GROFFEN, J ;
BOOTSMA, D ;
GROSVELD, G .
CELL, 1987, 51 (01) :33-40
[29]   Molecular and chromosomal mechanisms of resistance to imatinib (ST1571) therapy [J].
Hochhaus, A ;
Kreil, S ;
Corbin, AS ;
La Rosée, P ;
Müller, MC ;
Lahaye, T ;
Hanfstein, B ;
Schoch, C ;
Cross, N ;
Berger, U ;
Gschaidmeier, H ;
Druker, BJ ;
Hehlmann, R .
LEUKEMIA, 2002, 16 (11) :2190-2196
[30]  
Hochhaus A, 2002, BLOOD, V100, p164A