Vaddi Kris, Verstovsek Srdan, Kiladjian Jean-Jacques
Drug Discovery, Incyte Corporation, Wilmington, DE,
Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Blood Lymphat Cancer. 2016 May 12;6:7-19. doi: 10.2147/BLCTT.S101185. eCollection 2016.
Polycythemia vera (PV) is a chronic myeloproliferative neoplasm characterized by erythrocytosis and the presence of () V617F 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 drive the PV disease state. Traditional PV treatment strategies, including aspirin, phlebotomy, and cytoreduc-tive 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 discon-tinue 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.
真性红细胞增多症(PV)是一种慢性骨髓增殖性肿瘤,其特征为红细胞增多以及存在JAK2 V617F或类似突变。本综述总结了PV的病理生理学、传统治疗方案相关的挑战,以及芦可替尼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中的激活突变驱动了PV疾病状态。传统的PV治疗策略,包括阿司匹林、放血疗法以及如羟基脲等细胞减灭剂,对部分而非所有患者有临床益处,且可能无法充分治疗PV相关症状。此外,传统治疗方法存在潜在副作用,可能限制其使用并导致部分患者中断治疗。芦可替尼是一种口服小分子酪氨酸激酶抑制剂,是JAK1/JAK2的强效和选择性抑制剂。在美国,芦可替尼被批准用于对羟基脲反应不佳或不耐受的PV患者;在欧洲,它被批准用于对羟基脲耐药或不耐受的成年PV患者。在III期RESPONSE注册试验中,对于对羟基脲耐药或不耐受的PV患者,芦可替尼在控制血细胞比容水平、缩小脾脏体积以及改善PV相关症状和生活质量指标方面优于最佳可用疗法。在RESPONSE试验中,接受芦可替尼治疗的患者最常见的非血液学不良事件为头痛、腹泻、瘙痒和疲劳;血液学不良事件主要为1级或2级。在IIIb期非注册RELIEF试验中,对于羟基脲剂量稳定、总体病情得到良好控制但报告有疾病相关症状并转而使用芦可替尼的PV患者,与继续接受羟基脲治疗的患者相比,在症状控制改善方面存在不显著的趋势。更新的治疗指南对于教育医生了解芦可替尼在PV患者治疗中的作用将很重要。