Imatinib mesylate - In the treatment of gastrointestinal stromal tumours

被引:99
作者
Croom, KF [1 ]
Perry, CM [1 ]
机构
[1] Adis Int Ltd, Auckland 10, New Zealand
关键词
D O I
10.2165/00003495-200363050-00005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Imatinib mesylate (imatinib) is an orally administered competitive inhibitor of the tyrosine kinases associated with the KIT protein (stem cell factor receptor), ABL protein and platelet-derived growth factor receptors. The KIT tyrosine kinase is abnormally expressed in gastrointestinal stromal tumour (GIST), a rare neoplasm for which there has been no effective systemic therapy. In a randomised, nonblind, multicentre study that evaluated imatinib 400 or 600mg once daily in 147 patients with advanced GIST, confirmed partial responses were achieved in 54% of patients overall (median duration of follow-up was 288 days). Stable disease was experienced by 28% of patients and the estimated 1-year survival rate was 88%. Similar response rates were reported in a smaller, dose-escalation study, in which objective tumour response was a secondary endpoint. Although nearly all patients with GIST treated with imatinib experienced adverse events, most events were mild or moderate in nature. Severe or serious adverse events occurred in 21% of patients in the larger study, and included gastrointestinal or tumour haemorrhage.
引用
收藏
页码:513 / 522
页数:10
相关论文
共 44 条
  • [1] Attoub S, 2002, CANCER RES, V62, P4879
  • [2] Imatinib mesylate therapy in patients with gastrointestinal stromal tumors and impaired liver function
    Bauer, S
    Hagen, V
    Pielken, HJ
    Bojko, P
    Seeber, S
    Schütte, J
    [J]. ANTI-CANCER DRUGS, 2002, 13 (08) : 847 - 849
  • [3] Gastrointestinal stromal tumor workshop
    Berman, J
    O'Leary, TJ
    [J]. HUMAN PATHOLOGY, 2001, 32 (06) : 578 - 582
  • [4] BLANKE CD, 2001, CURR TREAT OPTIONS O, P485
  • [5] BLANKE CD, 2001, 37 ANN M AM SOC CL 1, V20, P1
  • [6] Buchdunger E, 1996, CANCER RES, V56, P100
  • [7] Buchdunger E, 2000, J PHARMACOL EXP THER, V295, P139
  • [8] CGP 57148, a tyrosine kinase inhibitor, inhibits the growth of cells expressing BCR-ABL, TEL-ABL, and TEL-PDGFR fusion proteins
    Carroll, M
    OhnoJones, S
    Tamura, S
    Buchdunger, E
    Zimmermann, J
    Lydon, NB
    Gilliland, DG
    Druker, BJ
    [J]. BLOOD, 1997, 90 (12) : 4947 - 4952
  • [9] *COMM PROP MED PRO, 2002, EUR PUBL ASS REP GLI
  • [10] Dagher R, 2002, CLIN CANCER RES, V8, P3034