追求治疗干预和克隆造血早期临床试验的蓝图。

IF 5.1 2区 医学 Q1 HEMATOLOGY
Tamanna Haque, Aditi Shastri, Pinkal Desai, Zhuoer Xie, Danielle Hammond, Zoe King, Ashwin Kishtagari, Yazan F. Madanat, Yasmin Abaza, Alexander J. Silver, Abhay Singh, Uma M. Borate, J. Brett Heimlich, David A. Slosky, Kelly L. Bolton, Mrinal S. Patnaik, Alexander G. Bick, Amit K. Verma, Siddhartha Jaiswal, David P. Steensma, Michael R. Savona
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引用次数: 0

摘要

克隆造血(CH)的年龄相关突变状态与多种不良健康结果相关。由于高风险的CH可导致进展性肿瘤或血管疾病,因此有兴趣开展临床试验以降低与CH相关的风险。鉴于CH的高患病率,临床试验的数据可能对筛查和治疗具有广泛的公共卫生意义。需要深思熟虑的考虑来设计既与临床相关又避免过度医疗化的试验。在此,我们总结了迄今为止关于CH的临床研究,并就如何设计以CH为中心的治疗性临床试验提供建议和指导。这些建议源于临床研究人员和科学家在2021年10月体细胞突变和疾病前期首届会议上的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A blueprint for pursuing therapeutic interventions and early phase clinical trials in clonal haematopoiesis

A blueprint for pursuing therapeutic interventions and early phase clinical trials in clonal haematopoiesis

The age-associated mutational state of clonal haematopoiesis (CH) is linked to multiple adverse health outcomes. As higher risk CH can lead to progressive neoplastic or vascular disease, there is interest in developing clinical trials to mitigate risk associated with CH. Given the high prevalence of CH, data from clinical trials could have broad public health implications for screening and therapy. Thoughtful consideration is needed to design trials that are both clinically relevant and avoid overmedicalization. Here, we summarize clinical studies of CH to date and provide suggestions and guidance on how to approach designing CH-focused therapeutic clinical trials. These recommendations are derived from discussions among clinical researchers and scientists emanating from the Inaugural Meeting on Somatic Mutations and Predisease in October 2021.

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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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