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吉拉西布在急性髓系白血病治疗中的应用。

Glasdegib in the treatment of acute myeloid leukemia.

机构信息

Department of Hematology, Medical University of Lodz, ul. Ciolkowskiego 2, 93-510 Lodz, Poland.

出版信息

Future Oncol. 2019 Oct;15(28):3219-3232. doi: 10.2217/fon-2019-0171. Epub 2019 Aug 21.

Abstract

Pharmacologic inhibition of the Hedgehog pathway significantly enhanced the sensitivity of leukemic cells to cytotoxic drugs. Glasdegib (PF-04449913; DAURISMO™) is a potent and selective oral inhibitor of the Hedgehog signaling pathway with clinical activity in patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), particularly in combination with chemotherapy. The results of Phase Ib/II studies evaluating safety and efficacy of glasdegib combined with chemotherapy in previously untreated patients with AML or high-risk myelodysplastic syndrome have recently been published. In the BRIGHT AML 1003 study, glasdegib in combination with low-dose cytarabine (LDAC) was well tolerated and demonstrated a significant 54% reduction in mortality compared with LDAC for AML patients. In 2018, the US FDA approved glasdegib in combination with LDAC for the treatment of newly diagnosed patients with AML who are 75 years old or older or who have co-morbidities that preclude use of intensive induction chemotherapy.

摘要

药物抑制 Hedgehog 通路显著提高了白血病细胞对细胞毒性药物的敏感性。玻璃酸酶(PF-04449913;DAURISMO™)是一种强效和选择性的 Hedgehog 信号通路抑制剂,在急性髓细胞白血病(AML)和骨髓增生异常综合征(MDS)患者中具有临床活性,特别是与化疗联合使用时。最近公布了评估玻璃酸酶联合化疗治疗初治 AML 或高危骨髓增生异常综合征患者的安全性和疗效的 Ib/II 期研究结果。在 BRIGHT AML 1003 研究中,玻璃酸酶联合低剂量阿糖胞苷(LDAC)治疗 AML 患者耐受性良好,与 LDAC 相比,死亡率显著降低了 54%。2018 年,美国 FDA 批准玻璃酸酶联合 LDAC 用于治疗年龄在 75 岁及以上或合并症不适合强化诱导化疗的新诊断 AML 患者。

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