伊马替尼
医学
慢性粒细胞白血病
疾病
肿瘤科
酪氨酸激酶
酪氨酸激酶抑制剂
内科学
费城染色体
甲磺酸伊马替尼
髓系白血病
免疫学
癌症
染色体易位
生物化学
化学
基因
受体
作者
Rüdiger Hehlmann,Andreas Hochhaus,Michele Baccarani
出处
期刊:The Lancet
[Elsevier BV]
日期:2007-07-01
卷期号:370 (9584): 342-350
被引量:494
标识
DOI:10.1016/s0140-6736(07)61165-9
摘要
Chronic myeloid leukaemia (CML) was the first neoplastic disease for which knowledge of the genotype led to a rationally designed therapy. As a result of its well known pathophysiology, straightforward diagnosis, well established prognostic factors, and treatment for the cause of disease, CML has been studied to an extent that far exceeds that expected from its frequency, and serves as a model disease for other cancers. Imatinib, an inhibitor of BCR-ABL tyrosine kinase, has revolutionised treatment of this disease, and is now recommended as standard treatment for chronic-phase CML. Interferon alfa is an acceptable alternative treatment in the early chronic phase for patients who do not tolerate imatinib. If imatinib treatment fails, allogeneic stem-cell transplantation, a dose increase of imatinib, or new drugs are recommended. Up to 87% of patients achieve complete cytogenetic remission, therefore we provide guidance for monitoring disease status. Many trials of new drugs and combination therapies that include imatinib are underway.
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