ruxolitinib (JAKAVI°)和真性红细胞增多症尚无定论。

Q4 Medicine Prescrire International Pub Date : 2016-10-01
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引用次数: 0

摘要

真性红细胞增多症(一种骨髓增生性综合征)患者发生血栓事件的风险增加。骨髓纤维化和转化为急性白血病也可在几年后发生。治疗是基于静脉切开术和低剂量(抗血小板)阿司匹林,有时联合羟基脲,一种细胞毒性药物。如果羟脲治疗失败或耐受性差,可使用其他多种药物,但目前尚无一致的治疗方法。Ruxolitinib抑制Janus酪氨酸激酶,在其他作用中,参与造血。Ruxolitinib已在欧盟被批准用于羟脲治疗失败或耐受性差的真性红细胞增多症患者。在这种情况下,ruxolitinib的临床评估是基于一项随机、非盲试验,与研究者选择的治疗方法相比,222名患者接受了32周的治疗。59%的病例选择羟基脲,即使患者有不可接受的不良反应或对药物的反应不足。研究者选择的其他治疗方法是否有效还不确定。鲁索非替尼组的放血频率低于对照组。由于长期评估不充分,在这种情况下,鲁索替尼的不良反应记录很少。在短期内,ruxolitinib引起贫血和血小板减少症,以及出血、潜在的严重感染、头痛、感觉障碍和体重增加。它也可能有其他免疫抑制剂的严重副作用。Ruxolitinib主要由细胞色素P450同工酶CYP3A4和CYP2C9代谢,产生多种药物相互作用的风险。Ruxolitinib在动物实验中显示胚胎毒性。实际上没有关于孕妇的数据。在实践中,关于ruxolitinib的利弊平衡的现有数据未能表明,与其他药物相比,该药物对真性红细胞增多症患者具有切实的进展,当羟基脲不适合时使用。
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ruxolitinib (JAKAVI°) and polycythaemia vera Inconclusive evaluation.

Patients with polycythaemia vera, a myeloproliferative syndrome, are at increased risk of thrombotic events. Marrow fibrosis and transformation to acute leukaemia can also occur after several years. Treatment is based on phlebotomy and aspirin at low (antiplatelet) doses, sometimes combined with hydroxycarbamide, a cytotoxic drug. Various other drugs are available if hydroxycarbamide fails or is poorly tolerated, but there is no consensus treatment. Ruxolitinib inhibits Janus tyrosine kinases, which are involved, among other roles, in haematopoiesis. Ruxolitinib has been authorised in the European Union for patients with polycythaemia vera in whom hydroxycarbamide has failed or is poorly tolerated. Clinical evaluation of ruxolitinib in this setting is based on a randomised, unblinded trial versus treatment chosen by the investigators, in 222 patients treated for 32 weeks. Hydroxycarbamide was chosen in 59% of cases, even though the patients had unacceptable adverse effects or an inadequate response to the drug. The efficacy of the investigators' other treatment choices was uncertain. Phlebotomy was less frequent in the ruxofitinib group than in the control group. The adverse effects of ruxotitinib in this situation are poorly documented, due to inadequate long-term assessment. In the short term, ruxolitinib causes anaemia and thrombocytopenia, as well as bleeding, potentially severe infections, headache, sensory disturbances, and weight gain. It is also likely to share the serious adverse effects of other immunosuppressants. Ruxolitinib is mainly metabolised by cytochrome P450 isoenzymes CYP3A4 and CYP2C9, creating a risk of multiple drug interactions. Ruxolitinib showed embryofetal toxicity in animal studies. Virtually no data are available in pregnant women. In practice, available data on the harm-benefit balance of ruxolitinib fail to show that this drug represents a tangible advance for patients with polycythaemia vera, as compared with other drugs used when hydroxycarbamide is unsuitable.

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Prescrire International
Prescrire International Medicine-Pharmacology (medical)
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