a Department of Medicine , Haraldsplass Deaconess Hospital , Bergen , Norway.
b Department of Medicine , Haukeland University Hospital , Bergen , Norway.
Expert Opin Investig Drugs. 2019 May;28(5):411-420. doi: 10.1080/13543784.2019.1597052. Epub 2019 Apr 5.
Acute lymphoblastic leukemia (ALL) with BCR-ABL1 translocation is an aggressive malignancy that is usually treated with intensive chemotherapy with the possibility of allogeneic stem cell transplantation. The encoded fusion protein may be important for leukemogenesis; clinical studies show that dasatinib has an antileukemic effect in combination with steroids alone or intensive chemotherapy. Areas covered: Relevant publications were identified through literature searches (the used terms being acute lymphoblastic leukemia plus dasatinib) in the PubMed database. We searched for original articles and reviews describing the pharmacology and clinical use of dasatinib in ALL with BCR-ABL1. The mechanism of action, pharmacology and clinical study findings are examined. Expert opinion: Dasatinib is associated with a high complete remission rate in ALL when used alone and in combination with steroids or intensive chemotherapy. However, mutations at T315 and F317 are associated with dasatinib resistance. Overall toxicity has been acceptable in these studies and no unexpected toxicity was observed. It is not known whether the antileukemic effect of dasatinib differs between subsets of BCR-ABL1 patients or is attributed to inhibition of the fusion protein alone, or a combined effect on several kinases, and whether dasatinib-containing combination treatment should be preferred in these patients instead of other emerging strategies, e.g. monoclonal antibodies.
急性淋巴细胞白血病(ALL)伴 BCR-ABL1 易位是一种侵袭性恶性肿瘤,通常采用强化化疗联合异体干细胞移植治疗。编码融合蛋白可能对白血病的发生起重要作用;临床研究表明达沙替尼联合类固醇或强化化疗具有抗白血病作用。
通过在 PubMed 数据库中进行文献检索(使用的术语为急性淋巴细胞白血病加达沙替尼),确定了相关出版物。我们检索了描述达沙替尼在伴有 BCR-ABL1 的 ALL 中的药理学和临床应用的原始文章和综述。研究了其作用机制、药理学和临床研究结果。
达沙替尼单独使用或与类固醇或强化化疗联合使用时,ALL 的完全缓解率较高。然而,T315 和 F317 突变与达沙替尼耐药相关。在这些研究中,整体毒性可接受,未观察到意外毒性。尚不清楚达沙替尼对不同 BCR-ABL1 患者亚组的抗白血病作用是否不同,或者是否归因于单独抑制融合蛋白,或者对几种激酶的联合作用,以及在这些患者中是否应首选包含达沙替尼的联合治疗而不是其他新兴策略,例如单克隆抗体。