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

机译:PCI-32765:一种新型的布鲁顿酪氨酸激酶抑制剂,用于治疗淋巴恶性肿瘤

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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.
机译:简介:淋巴恶性肿瘤的治疗和管理方式已发生重大转变。治疗已经从常规化学疗法转向靶向治疗。新型试剂(例如单克隆抗体,蛋白酶体抑制剂和免疫调节衍生物)的成功引发了对抑制新途径的进一步研究。布鲁顿酪氨酸激酶(Btk)途径是B细胞受体(BCR)途径的下游介体,对B细胞的产生和维持至关重要,并且是潜在的治疗靶标。涵盖的领域:本综述将总结Btk途径的最新知识及其在淋巴样恶性肿瘤中的作用。它还将在临床前和临床环境中讨论有关PCI-32765的当前数据。专家意见:PCI-32765是一种口服不可逆Btk抑制剂,在慢性淋巴细胞性白血病(CLL)和非霍奇金淋巴瘤(NHL)中具有强大的效力,并且具有临床前和临床活性。一期研究表明,它具有良好的耐受性并具有出色的安全性。作为单一药物并与其他靶向和常规疗法结合的进一步研究正在进行中。 PCI-32765是一种非常有前途的靶向疗法,这些试验的数据将最终决定其未来的作用和成功。

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