Ruxolitinib: a targeted treatment option for patients with polycythemia vera

K. Vaddi, S. Verstovsek, J. Kiladjian
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引用次数: 2

Abstract

Polycythemia vera (PV) is a chronic myeloproliferative neoplasm characterized by erythrocytosis and the presence of Janus kinase (JAK) 2V617F or similar mutations. This review summarizes the pathophysiology of PV, the challenges associated with traditional treatment options, and the scientific rationale and supportive clinical evidence for targeted therapy with ruxolitinib. Accumulating evidence indicates that activating mutations in JAK2 drive the PV disease state. Traditional PV treatment strategies, including aspirin, phlebotomy, and cytoreductive agents such as hydroxyurea, provide clinical benefits for some but not all patients and may not adequately treat PV-related symptoms. Furthermore, traditional treatment approaches are associated with potential side effects that may limit their usage and lead some patients to discontinue the treatment. Ruxolitinib is an orally available small-molecule tyrosine kinase inhibitor that is a potent and selective inhibitor of JAK1/JAK2. Ruxolitinib is approved in the US for patients with PV with an inadequate response or intolerance to hydroxyurea and in Europe for adults with PV who are resistant to or intolerant of hydroxyurea. In the Phase III RESPONSE registration trial, ruxolitinib was superior to the best available therapy in patients with PV who were resistant to or intolerant of hydroxyurea in controlling hematocrit levels, reducing spleen volume, and improving PV-related symptoms and quality-of-life measures. The most common nonhematologic adverse events in ruxolitinib-treated patients were headache, diarrhea, pruritus, and fatigue in the RESPONSE trial; hematologic adverse events were primarily grade 1 or 2. In the Phase IIIb nonregistration RELIEF trial, there were nonsignificant trends toward an improved symptom control in patients with PV on a stable hydroxyurea dose who were generally well controlled but reported disease-associated symptoms and switched to ruxolitinib vs those who continued hydroxyurea therapy. Updated treatment guidelines will be important for educating physicians about the role of ruxolitinib in the treatment of patients with PV.
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鲁索利替尼:真性红细胞增多症患者的靶向治疗选择
真性红细胞增多症(PV)是一种慢性骨髓增生性肿瘤,其特征是红细胞增多和Janus激酶(JAK) 2V617F或类似突变的存在。本文综述了PV的病理生理学,与传统治疗方案相关的挑战,以及ruxolitinib靶向治疗的科学依据和支持性临床证据。越来越多的证据表明JAK2的激活突变驱动PV疾病状态。传统的PV治疗策略,包括阿司匹林、静脉切开术和细胞减减剂(如羟基脲),对一些但不是所有患者有临床益处,可能不能充分治疗PV相关症状。此外,传统的治疗方法与潜在的副作用有关,这些副作用可能会限制其使用并导致一些患者停止治疗。Ruxolitinib是一种口服小分子酪氨酸激酶抑制剂,是一种有效的选择性JAK1/JAK2抑制剂。Ruxolitinib在美国被批准用于对羟基脲反应不足或不耐受的PV患者,在欧洲被批准用于对羟基脲耐药或不耐受的PV成人患者。在III期应答注册试验中,ruxolitinib在控制红细胞压积水平、减少脾脏体积、改善PV相关症状和生活质量方面优于对羟基脲耐药或不耐受的PV患者的最佳可用治疗。在RESPONSE试验中,ruxolitinib治疗的患者最常见的非血液学不良事件是头痛、腹泻、瘙痒和疲劳;血液学不良事件主要为1级或2级。在iii期非注册的RELIEF试验中,在接受稳定羟脲剂量的PV患者中,症状控制改善的趋势不显著,这些患者通常控制良好,但报告了疾病相关症状,并且与继续羟脲治疗的患者相比,转而使用鲁索利替尼。更新的治疗指南对于教育医生ruxolitinib在PV患者治疗中的作用非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
7.10%
发文量
16
审稿时长
16 weeks
期刊介绍: Blood and Lymphatic Cancer: Targets and Therapy is an international, peer reviewed, open access journal focusing on blood and lymphatic cancer research, identification of therapeutic targets, and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for the cancer patient. Specific topics covered in the journal include: Epidemiology, detection and screening Cellular research and biomarkers Identification of biotargets and agents with novel mechanisms of action Optimal clinical use of existing anticancer agents, including combination therapies Radiation, surgery, bone marrow transplantation Palliative care Patient adherence, quality of life, satisfaction Health economic evaluations.
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