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血浆循环肿瘤 DNA 与影像学肿瘤负担的相关性。

The Correlation between Plasma Circulating Tumor DNA and Radiographic Tumor Burden.

机构信息

Department of Pathology and Laboratory Medicine, University of Louisville, Louisville, Kentucky.

Hiram C. Polk, Jr, MD, Department of Surgery, University of Louisville, Louisville, Kentucky; UofL Health-Brown Cancer Center, University of Louisville, Louisville, Kentucky.

出版信息

J Mol Diagn. 2024 Nov;26(11):952-961. doi: 10.1016/j.jmoldx.2024.07.001. Epub 2024 Aug 22.

Abstract

Conventional blood-based biomarkers and radiographic imaging are excellent for use in monitoring different aspects of malignant disease, but given their specific shortcomings, their integration with other, complementary markers such as plasma circulating tumor DNA (ctDNA) will be beneficial toward a precision medicine-driven future. Plasma ctDNA analysis utilizes the measurement of cancer-specific molecular alterations in a variety of bodily fluids released by dying tumor cells to monitor and profile response to therapy, and is being employed in several clinical scenarios. Plasma concentrations of ctDNA have been reported to correlate with tumor burden. However, the strength of this association is generally poor and highly variable, confounding the interpretation of longitudinal plasma ctDNA measurements in conjunction with routine radiographic assessments. Herein is discussed what is currently understood with respect to the fundamental characteristics of tumor growth that dictate plasma ctDNA concentrations, with a perspective on its interpretation in conjunction with radiographically determined tumor burden assessments.

摘要

传统的基于血液的生物标志物和影像学检查非常适用于监测恶性疾病的不同方面,但鉴于它们的具体缺点,将它们与其他互补标志物(如血浆循环肿瘤 DNA [ctDNA])结合使用将有助于实现精准医疗的未来。血浆 ctDNA 分析利用测量各种体液中由死亡肿瘤细胞释放的癌症特异性分子改变,以监测和分析对治疗的反应,并且正在几种临床情况下得到应用。已经报道血浆 ctDNA 浓度与肿瘤负担相关。然而,这种关联的强度通常较差且高度可变,使得与常规影像学评估相结合的纵向血浆 ctDNA 测量的解释变得复杂。本文讨论了目前对决定血浆 ctDNA 浓度的肿瘤生长基本特征的理解,并从与影像学确定的肿瘤负担评估相结合的角度对其进行了解释。

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