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The CYTO-PV: A Large-Scale Trial Testing the Intensity of CYTOreductive Therapy to Prevent Cardiovascular Events in Patients with Polycythemia Vera

机译:CYTO-PV:大规模试验,测试了CYTO还原疗法的强度,以预防真性红细胞增多症患者的心血管事件

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Polycythemia vera (PV) is a chronic myeloproliferative disorder whose major morbidity and mortality are thrombohaemorragic events. Current guidelines advise maintaining hematocrit (HCT) level below 45% in males and 42% in females. Such targets lean on pathophysiological reasoning, while evidence from ECLAP and PVSG-01, the two largest prospective studies in this disease, suggests no difference in the rate of thrombosis in patients maintained at different HCT values below 50%–52%. Cytoreductive therapy in PV (CYTO-PV) is a multicenter, randomized, and controlled trial assess the benefit/risk profile of cytoreductive therapy with phlebotomy or HU aimed at maintaining HCT < 45% versus maintaining HCT in the range 45%–50%. CYTO-PV is being conducted in the framework of the Gruppo Italiano Malattie Ematologiche nell'Adulto (GIMEMA) and is funded by the Italian Drug Agency (AIFA). It is an independent trial with broad recruitment criteria to mimic clinical practice. We describe here the study and its advancement status.Conclusions. Clinical research in rare disease can be carried out with limited funds, provided a research hypothesis is felt as clinically relevant by a scientific community willing to share knowledge on the outcome of clinical practice, thus producing scientific results useful to improve treatment and prognosis of patients.
机译:真性红细胞增多症(PV)是一种慢性骨髓增生性疾病,其主要发病率和死亡率是血栓出血事件。当前的指南建议将男性的血细胞比容(HCT)水平保持在45%以下,女性的血细胞比容保持在42%以下。这样的靶标依赖于病理生理学推理,而来自ECLAP和PVSG-01(这是该疾病的两个最大的前瞻性研究)的证据表明,维持在低于50%–52%的不同HCT值的患者血栓形成率没有差异。 PV的细胞减少疗法(CYTO-PV)是一项多中心,随机对照试验,旨在评估静脉放血或HU进行细胞减少疗法的获益/风险,旨在维持HCT <45%,而将HCT维持在45%-50%。 CYTO-PV在Gruppo Italiano Malattie Ematologiche nell'Adulto(GIMEMA)的框架内进行,并由意大利药品管理局(AIFA)资助。这是一项具有广泛募集标准的模仿临床实践的独立试验。我们在这里描述了这项研究及其进展情况。只要愿意共享临床实践成果知识的科学界认为研究假设与临床相关,就可以用有限的资金开展罕见疾病的临床研究,从而产生有助于改善患者治疗和预后的科学成果。

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