Asciminib in chronic myeloid leukemia

被引:3
|
作者
Assanto, Giovanni Manfredi [1 ]
Scalzulli, Emilia [1 ]
Breccia, Massimo [1 ,2 ]
机构
[1] Az Policlin Umberto I Sapienza Univ, Dept Translat & Precis Med, Hematol, Rome, Italy
[2] Sapienza Univ, Dept Translat & Precis Med, Hematol, Via Benevento 6, I-00161 Rome, Italy
关键词
Asciminib; Chronic myeloid leukemia; BCR-ABL kinase inhibitors; STAMP (specifically; targeting the ABL myristoyl pocket) inhibitors; Hematologic malignancies; T315I mutation; IMATINIB-RESISTANT; CHRONIC-PHASE; FOLLOW-UP; DASATINIB;
D O I
10.1358/dot.2022.58.10.3441853
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the fact that, in the last years, life expectancy of chronic myeloid leukemia (CML) patients has reached that of the normal population, a significant propor-tion of CML patients is likely to fail treatment with first-or second-generation tyrosine kinase inhibitors (TKIs). Failure to first-line treatment is commonly due to molecular resistance or unbearable toxicity. New specific compounds are tested in this setting to fulfill this unmet clinical need in CML; of these, asciminib has shown efficacy based on allosteric inhibition which allows to overcome resistance and off-target toxicity. This review aims to cover how asciminib will change the therapeutic scenario of CML, highlight-ing its mechanism of action, pharmacokinetics, effi-cacy and toxicity. Asciminib will be a possible option as third-line therapy for patients carrying resistant mutations, such as T315I, and/or not eligible for treat-ment with other TKIs.
引用
收藏
页码:479 / 489
页数:11
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