PCI-32765: a novel Bruton's tyrosine kinase inhibitor for the treatment of lymphoid malignancies

布鲁顿酪氨酸激酶 伊布替尼 慢性淋巴细胞白血病 癌症研究 酪氨酸激酶 医学 淋巴瘤 免疫学 靶向治疗 临床试验 酪氨酸激酶抑制剂 白血病 内科学 癌症 受体
作者
Eric S. Winer,Randall R Ingham,Jorge J. Castillo
出处
期刊:Expert Opinion on Investigational Drugs [Informa]
卷期号:21 (3): 355-361 被引量:39
标识
DOI:10.1517/13543784.2012.656199
摘要

Introduction: There has been a significant paradigm shift in the manner in which lymphoid malignancies are treated and managed. Treatment has been moving away from conventional chemotherapy and towards targeted therapy. The success of new classes of agents such as monoclonal antibodies, proteasome inhibitors and immunomodulatory derivatives has sparked further searches for novel pathways to inhibit. The Bruton's tyrosine kinase (Btk) pathway is a downstream mediator of the B-cell receptor (BCR) pathway, which is crucial in B-cell production and maintenance, and a potential therapeutic target. Areas covered: This review will summarize the current knowledge of the Btk pathway and its role in lymphoid malignancies. It will also discuss the present data about PCI-32765 in both the preclinical and clinical setting. Expert opinion: PCI-32765 is an oral irreversible Btk inhibitor with high potency and both preclinical and clinical activity in chronic lymphocytic leukemia (CLL) and non-Hodgkin's lymphoma (NHL). Phase I studies have demonstrated that it is well tolerated and has an excellent safety profile. Further studies are ongoing as a single agent and in combination with other targeted and conventional therapies. PCI-32765 is a very promising targeted therapy, and the data from these trials will ultimately decide its future role and success.
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