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Pharmacobiological Approach for the Clinical Development of Ruxolitinib in Myeloproliferative Neoplasms

机译:鲁索替尼在骨髓增生性肿瘤中临床发展的药物生物学方法

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摘要

Ruxolitinib, a JAK1 and JAK2 inhibitor drug, has recently been approved for the treatment of patients with high- or intermediate-risk myelofibrosis with symptomatic splenomegaly. Ruxolitinib is the first clinically useful targeted therapy in Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs). The aim of this paper is to indicate pharmacobiological aspects of ruxolitinib within the potential context of MPNs. Pharmacobiological assessments, in addition to knowledge of the risk profile for ruxolitinib in MPNs, are required. We propose hypotheses based on our experience in a splenectomized MPN patient with hyperproliferative bone marrow and moderate fibrosis receiving ruxolitinib. We believe that a true clinical development approach for this drug should include pharmacobiological assessments for ruxolitinib in addition to the disease risk profile of MPNs.
机译:Ruxolitinib是一种JAK1和JAK2抑制剂药物,最近已被批准用于治疗有症状性脾肿大的高危或中危骨髓纤维化患者。鲁索替尼是费城染色体阴性骨髓增生性肿瘤(MPN)中的第一种临床有用的靶向治疗。本文的目的是在MPNs的潜在背景下指出鲁索替尼的药理生物学方面。除了需要了解MPN中鲁索替尼的风险概况外,还需要进行药理生物学评估。根据我们在接受ruxolitinib的脾过度增殖性骨髓和中度纤维化的脾切除MPN患者中的经验,我们提出了假设。我们认为,该药物的真正临床开发方法除了MPN的疾病风险谱外,还应包括鲁索替尼的药理生物学评估。

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