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What are the current treatment approaches for patients with polycythemia vera and essential thrombocythemia?

机译:对于真性红细胞增多症和原发性血小板增多症患者目前有哪些治疗方法?

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摘要

Polycythemia vera (PV) and essential thrombocythemia (ET) are chronic myeloproliferative neoplasms that are characterized by thrombohemorrhagic complications, symptom burden, and impaired survival mainly due to thrombosis, progression to myelofibrosis, and transformation to acute leukemia. In this manuscript, we will review the most recent changes in diagnostic criteria, the improvements in risk stratification, and the “state of the art” in the daily management of these disorders. The role of conventional therapies and novel agents, interferon α and the JAK2 inhibitor ruxolitinib, is critically discussed based on the results of a few basic randomized clinical studies. Several unmet needs remain, above all, the lack of a curative approach that might overcome the still burdensome morbidity and mortality of these hematologic neoplasms, as well as the toxicities associated with therapeutic agents.
机译:真性红细胞增多症(PV)和原发性血小板增多症(ET)是慢性骨髓增生性肿瘤,其特征在于血栓出血性并发症,症状负担和生存受损,主要是由于血栓形成,进展为骨髓纤维化和向急性白血病的转化。在本手稿中,我们将回顾诊断标准的最新变化,风险分层的改善以及这些疾病的日常管理中的“最新技术”。基于一些基础随机临床研究的结果,对传统疗法和新型药物干扰素α和JAK2抑制剂鲁索替尼的作用进行了严格讨论。最重要的是,仍然缺乏一些治愈方法可以克服这些血液肿瘤的高发病率和死亡率以及与治疗药物有关的毒性,这是一些尚待解决的需求。

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