Adis, a Wolters Kluwer Business, Auckland, New Zealand.
Drugs. 2011 Sep 10;71(13):1771-95. doi: 10.2165/11207580-000000000-00000.
Dasatinib (Sprycel®) is an orally administered small molecule inhibitor of multiple tyrosine kinases, including BCR-ABL and SRC family kinases, which is indicated for the treatment of adults with newly diagnosed chronic-phase chronic myeloid leukaemia (CML), CML (chronic-, accelerated- or blast-phase) with resistance or intolerance to prior therapy, including imatinib, or Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukaemia (ALL) with resistance or intolerance to prior therapy. Dasatinib is ≈325-fold more active than imatinib in inhibiting wild-type ABL kinase in vitro and is active against a wide variety of imatinib-resistant BCR-ABL mutants, except for T315I. This article reviews the efficacy and tolerability of dasatinib in the treatment of patients with newly diagnosed chronic-phase CML or imatinib-resistant or -intolerant CML or Ph+ ALL, as well as summarizing its pharmacological properties. In clinical trials, oral dasatinib was effective in achieving major or complete cytogenetic responses in both newly diagnosed and imatinib-resistant or -intolerant chronic-phase CML. Dasatinib was likewise effective in achieving major or overall haematological responses in imatinib-resistant or -intolerant, accelerated- or blast-phase CML, or Ph+ ALL. Responses were rapidly achieved within 1-3 months and were durable over 1-5 years of follow-up. The majority of adverse events with dasatinib were of mild to moderate severity. Fluid retention (including pleural effusion) was the most common adverse event. Haematological abnormalities were common and cytopenias were the most common grade 3/4 adverse events. Dasatinib 100 mg administered once daily was as effective as dasatinib 70 mg administered twice daily, and was better tolerated, being associated with lower incidences of pleural effusion and grade 3/4 thrombocytopenia, in particular. Dasatinib was more effective than high-dose imatinib in the treatment of patients with imatinib-resistant chronic-phase CML and was more effective than standard dosages of imatinib, as well as being associated with less frequent fluid retention, in patients with newly diagnosed chronic-phase CML. Dasatinib was generally equally effective in patients with or without BCR-ABL mutations at baseline. Therefore, oral dasatinib is a highly effective once-daily therapy for the first-line treatment of newly diagnosed patients with chronic-phase CML, as well as for the treatment of patients with imatinib-resistant or -intolerant chronic- and advanced-phase CML or Ph+ ALL.
达沙替尼(Sprycel®)是一种口服小分子抑制剂,可抑制多种酪氨酸激酶,包括 BCR-ABL 和 SRC 家族激酶,用于治疗新诊断的慢性期慢性髓性白血病(CML)、对先前治疗(包括伊马替尼)有耐药或不耐受的 CML(慢性期、加速期或急变期)或对先前治疗有耐药或不耐受的费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)的成人患者。达沙替尼在体外抑制野生型 ABL 激酶的活性比伊马替尼高约 325 倍,对多种伊马替尼耐药的 BCR-ABL 突变体有效,除 T315I 外。本文综述了达沙替尼治疗新诊断的慢性期 CML 或伊马替尼耐药或不耐受的 CML 或 Ph+ ALL 患者的疗效和耐受性,并总结了其药理学特性。在临床试验中,口服达沙替尼在新诊断和伊马替尼耐药或不耐受的慢性期 CML 中均能有效实现主要或完全细胞遗传学反应。达沙替尼在伊马替尼耐药或不耐受的加速期或急变期 CML 或 Ph+ ALL 中也能有效实现主要或总体血液学反应。反应在 1-3 个月内迅速获得,在 1-5 年的随访中具有持久性。达沙替尼的大多数不良反应为轻至中度。体液潴留(包括胸腔积液)是最常见的不良反应。血液学异常很常见,血小板减少症是最常见的 3/4 级不良反应。达沙替尼 100mg 每日 1 次给药与达沙替尼 70mg 每日 2 次给药同样有效,且耐受性更好,与较低的胸腔积液发生率和 3/4 级血小板减少症发生率相关,尤其是如此。达沙替尼在治疗伊马替尼耐药的慢性期 CML 患者方面比高剂量伊马替尼更有效,与标准剂量的伊马替尼相比,也更有效,且较少发生体液潴留。达沙替尼在基线时有或没有 BCR-ABL 突变的患者中均同样有效。因此,口服达沙替尼是一种高效的每日一次治疗药物,适用于新诊断的慢性期 CML 患者的一线治疗,以及用于治疗伊马替尼耐药或不耐受的慢性期和进展期 CML 或 Ph+ ALL 患者。