Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Urology, The James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cancer Res. 2022 Nov 15;82(22):4107-4113. doi: 10.1158/0008-5472.CAN-22-0985.
Clonal hematopoiesis of indeterminate potential (CHIP) refers to the expansion of cells of hematopoietic lineage that carry acquired somatic alterations associated with hematologic malignancies. The most commonly altered genes giving rise to CHIP are DNMT3A, TET2, and ASXL1. However, advanced sequencing technologies have resulted in highly sensitive detection of clonal hematopoiesis beyond these known driver genes. In practice, CHIP is commonly identified as an incidental finding in liquid and tissue biopsies of patients with solid tumors. CHIP can have broad clinical consequences, given its association with hematologic malignancies and nonmalignant diseases. CHIP can also interfere with next-generation DNA sequencing results, so clinicians should pay careful attention when these results are being used to guide therapy. Future research is needed to determine how solid tumor malignancies and their treatments alter the progression of CHIP, and in turn, how CHIP might be used to improve treatment selection and outcomes for patients with solid tumors.
不定潜能克隆性造血 (CHIP) 是指携带与血液系统恶性肿瘤相关的获得性体细胞改变的造血谱系细胞的扩增。导致 CHIP 的最常见改变基因是 DNMT3A、TET2 和 ASXL1。然而,先进的测序技术已实现了对这些已知驱动基因以外的克隆性造血的高度敏感检测。实际上,CHIP 通常作为实体瘤患者的液体和组织活检中的偶然发现而被识别。鉴于 CHIP 与血液系统恶性肿瘤和非恶性疾病相关,因此其具有广泛的临床后果。CHIP 也可能会干扰下一代 DNA 测序结果,因此在使用这些结果来指导治疗时,临床医生应谨慎注意。未来的研究需要确定实体瘤恶性肿瘤及其治疗如何改变 CHIP 的进展,以及反过来,CHIP 如何用于改善实体瘤患者的治疗选择和结果。