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

Thrombosis Pub Date : 2011-01-01 Epub Date: 2011-05-17 DOI:10.1155/2011/794240
Roberto Marchioli, Guido Finazzi, Giorgina Specchia, Arianna Masciulli, Maria Rosaria Mennitto, Tiziano Barbui
{"title":"The CYTO-PV: A Large-Scale Trial Testing the Intensity of CYTOreductive Therapy to Prevent Cardiovascular Events in Patients with Polycythemia Vera.","authors":"Roberto Marchioli,&nbsp;Guido Finazzi,&nbsp;Giorgina Specchia,&nbsp;Arianna Masciulli,&nbsp;Maria Rosaria Mennitto,&nbsp;Tiziano Barbui","doi":"10.1155/2011/794240","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":75222,"journal":{"name":"Thrombosis","volume":"2011 ","pages":"794240"},"PeriodicalIF":0.0000,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2011/794240","citationCount":"54","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Thrombosis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2011/794240","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2011/5/17 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 54

Abstract

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.

Abstract Image

Abstract Image

Abstract Image

CYTO-PV:一项大规模试验,测试细胞减少治疗强度以预防真性红细胞增多症患者心血管事件。
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。目前的指南建议将男性和女性的红细胞压积(HCT)水平分别维持在45%和42%以下。这些靶点依赖于病理生理推理,而来自ECLAP和PVSG-01这两项最大的前瞻性研究的证据表明,在HCT值低于50%-52%的不同患者中,血栓形成率没有差异。PV中的细胞减少疗法(CYTO-PV)是一项多中心、随机、对照试验,评估细胞减少疗法联合静脉切开或HU的获益/风险,目的是维持HCT < 45%与维持HCT在45%-50%之间。CYTO-PV是在Gruppo Italiano Malattie Ematologiche nell'Adulto (GIMEMA)的框架内进行的,由意大利药品管理局(AIFA)资助。这是一项独立的试验,具有广泛的招募标准来模拟临床实践。本文介绍了这方面的研究和进展情况。结论。罕见病的临床研究可以在有限的资金下进行,前提是研究假设被一个愿意分享临床实践结果的科学界认为具有临床相关性,从而产生有助于改善患者治疗和预后的科学结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信