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酪氨酸激酶抑制剂对费城染色体阳性急性淋巴细胞白血病患者预后的影响。

Impact of tyrosine kinase inhibitors on patient outcomes in Philadelphia chromosome-positive acute lymphoblastic leukaemia.

作者信息

Gruber Franz, Mustjoki Satu, Porkka Kimmo

机构信息

Department of Pharmacology, University of Tromso, Tromso, Norway.

出版信息

Br J Haematol. 2009 Jun;145(5):581-97. doi: 10.1111/j.1365-2141.2009.07666.x. Epub 2009 Apr 15.

Abstract

Acute lymphoblastic leukaemia (ALL) is a heterogeneous disease that is often associated with several chromosomal and molecular abnormalities. Patients who have the Philadelphia (Ph) chromosome and associated BCR-ABL1 oncogene have a particularly poor prognosis. Currently, allogeneic haematopoietic stem cell transplantation (allo-HSCT) is the only known curative treatment for Ph+ ALL and facilitating allo-HSCT in eligible patients is a key treatment goal. However, many patients relapse after allo-HSCT, particularly those with measurable residual disease prior to transplantation, and a significant percentage of patients are ineligible for allo-HSCT, particularly older patients. Hence, many patients require additional/alternative therapies to prolong survival. Studies are ongoing to determine the most effective first-line drug regimens for patients who subsequently undergo allo-HSCT and ineligible patients. Tyrosine kinase inhibitors targeted to Bcr-Abl are important novel therapies for Ph+ ALL. Although imatinib administered in combination with chemotherapy is established as the current first-line strategy, relapse is common, even among allo-HSCT recipients. Emerging data indicate that more potent multi-targeted kinase inhibitors (including dasatinib, nilotinib, and bosutinib) have promising efficacy in the first- or second-line setting. Here, the evidence base for existing drug treatments for Ph+ ALL is discussed and emerging therapeutic strategies are explored.

摘要

急性淋巴细胞白血病(ALL)是一种异质性疾病,常与多种染色体和分子异常相关。携带费城(Ph)染色体及相关BCR-ABL1癌基因的患者预后尤其差。目前,异基因造血干细胞移植(allo-HSCT)是已知的唯一可治愈Ph+ ALL的治疗方法,促使符合条件的患者接受allo-HSCT是关键的治疗目标。然而,许多患者在allo-HSCT后复发,尤其是那些移植前有可测量残留疾病的患者,并且相当比例的患者不符合allo-HSCT的条件,特别是老年患者。因此,许多患者需要额外的/替代疗法来延长生存期。正在进行研究以确定随后接受allo-HSCT的患者和不符合条件的患者最有效的一线药物方案。靶向Bcr-Abl的酪氨酸激酶抑制剂是Ph+ ALL重要的新型治疗方法。尽管伊马替尼联合化疗已被确立为当前的一线策略,但复发很常见,即使在allo-HSCT受者中也是如此。新出现的数据表明,更有效的多靶点激酶抑制剂(包括达沙替尼、尼洛替尼和博舒替尼)在一线或二线治疗中具有有前景的疗效。在此,讨论了Ph+ ALL现有药物治疗的证据基础,并探索了新出现的治疗策略。

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