Dasatinib as an investigational drug for the treatment of Philadelphia chromosome-positive acute lymphoblastic leukemia in adults

被引:17
作者
Brattas, Marte Karen [1 ]
Reikvam, Hakon [2 ]
Tvedt, Tor Henrik Anderson [2 ]
Bruserud, Oystein [2 ,3 ]
机构
[1] Haraldsplass Deaconess Hosp, Dept Med, Bergen, Norway
[2] Haukeland Hosp, Dept Med, Bergen, Norway
[3] Univ Bergen, Dept Clin Sci, Sect Hematol, Bergen, Norway
关键词
Acute lymphoblastic leukemia; BCR-ABL; chemotherapy; clinical studies; dasatinib; imatinib; immunomodulation; TYROSINE KINASE INHIBITOR; MOLECULAR RESPONSE; SUPPRESSOR-CELLS; MYELOID-LEUKEMIA; BLINATUMOMAB; IMATINIB; COMBINATION; RESISTANCE; EXPANSION; EFFICACY;
D O I
10.1080/13543784.2019.1597052
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: 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.
引用
收藏
页码:411 / 420
页数:10
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