Haque Tamanna, Shastri Aditi, Desai Pinkal, Xie Zhuoer, Hammond Danielle, King Zoe, Kishtagari Ashwin, Madanat Yazan F, Abaza Yasmin, Silver Alexander J, Singh Abhay, Borate Uma M, Heimlich J Brett, Slosky David A, Bolton Kelly L, Patnaik Mrinal S, Bick Alexander G, Verma Amit K, Jaiswal Siddhartha, Steensma David P, Savona Michael R
Department of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Division of Hematologic Malignancies, Department of Oncology, Montefiore-Einstein Comprehensive Cancer Center, Bronx, New York, USA.
Br J Haematol. 2025 Feb;206(2):416-427. doi: 10.1111/bjh.19925. Epub 2024 Dec 9.
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.
克隆性造血(CH)的年龄相关突变状态与多种不良健康结局相关。由于高风险CH可导致进行性肿瘤或血管疾病,因此人们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,临床试验数据可能对筛查和治疗具有广泛的公共卫生意义。需要进行深入思考,以设计出既具有临床相关性又能避免过度医疗的试验。在此,我们总结了迄今为止CH的临床研究,并就如何设计以CH为重点的治疗性临床试验提供建议和指导。这些建议源自临床研究人员和科学家在2021年10月举行的体细胞突变与疾病前状态首届会议上的讨论。