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靶向性慢性粒细胞白血病治疗:控制耐药性,寻求治愈方法。

Targeted CML therapy: controlling drug resistance, seeking cure.

作者信息

O'Hare Thomas, Corbin Amie S, Druker Brian J

机构信息

Howard Hughes Medical Institute, Oregon Health & Science University Cancer Institute, L592, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA.

出版信息

Curr Opin Genet Dev. 2006 Feb;16(1):92-9. doi: 10.1016/j.gde.2005.11.002. Epub 2005 Dec 15.

Abstract

Targeted cancer therapy with imatinib (Gleevec) has the capability to drive chronic myeloid leukemia (CML) into clinical remission. Some patients, particularly those with advanced disease, develop resistance to imatinib. To counteract this problem, two new BCR-ABL kinase inhibitors for imatinib-refractory disease are currently in clinical trials: the imatinib derivative AMN107 and the dual-specificity SRC/ABL inhibitor dasatinib. Using imatinib to reduce leukemic burden also facilitates the detailed investigation into how the persistence of CML disease depends on BCR-ABL signaling, particularly within the leukemic stem cell compartment. Mathematical models of drug resistance and disease relapse, in addition to experimental systems that recapitulate crucial aspects of advanced disease have deepened our understanding of CML biology. Together, these advances are contributing to a high level of disease control, and might ultimately lead to disease eradication.

摘要

使用伊马替尼(格列卫)进行的靶向癌症治疗能够使慢性粒细胞白血病(CML)进入临床缓解期。一些患者,尤其是那些患有晚期疾病的患者,会对伊马替尼产生耐药性。为了解决这个问题,目前有两种用于治疗伊马替尼难治性疾病的新型BCR-ABL激酶抑制剂正在进行临床试验:伊马替尼衍生物AMN107和双特异性SRC/ABL抑制剂达沙替尼。使用伊马替尼减轻白血病负担也有助于详细研究CML疾病的持续存在如何依赖于BCR-ABL信号传导,特别是在白血病干细胞区室中。除了能够概括晚期疾病关键方面的实验系统外,耐药性和疾病复发的数学模型也加深了我们对CML生物学的理解。这些进展共同促成了高水平的疾病控制,并最终可能导致疾病根除。

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