期刊
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
卷 98, 期 -, 页码 200-210出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.critrevonc.2015.10.013
关键词
Polo-like kinase; Acute myeloid leukemia; Myelodysplastic syndromes; Drug development
资金
- Ariad Pharmaceuticals
- Incyte, Inc.
- Astex Pharmaceuticals
- Incyte Inc
- Spectrum Pharmaceuticals, Inc.
Polo-like kinases (Plk) are key regulators of the cell cycle and multiple aspects of mitosis. Two agents that inhibit the Plk signaling pathway have shown promising activity in patients with hematologic malignancies and are currently in phase III trials. Volasertib is a Plk inhibitor under evaluation combined with low-dose cytarabine in older patients with acute myeloid leukemia (AML) ineligible for intensive induction therapy. Rigosertib, a dual inhibitor of the Plk and phosphatidylinosito13-kinase pathways, is under investigation in patients with myelodysplastic syndrome (MDS) who have failed azacitidine or decitabine treatment. The prognosis for patients with AML, who are ineligible for intensive induction therapy, and for those with MDS refractory/relapsed after a hypomethylating agent, remains poor. Novel approaches, such as Plk inhibitors, are urgently needed for these patients. Here, we provide a comprehensive overview of the current state of development of Plk inhibitors for the treatment of hematologic malignancies. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
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