Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California.
Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Cancer Discov. 2021 Dec 1;11(12):2968-2986. doi: 10.1158/2159-8290.CD-21-0634.
Growing evidence demonstrates that circulating tumor DNA (ctDNA) minimal residual disease (MRD) following treatment for solid tumors predicts relapse. These results suggest that ctDNA MRD could identify candidates for adjuvant therapy and measure response to such treatment. Importantly, factors such as assay type, amount of ctDNA release, and technical and biological background can affect ctDNA MRD results. Furthermore, the clinical utility of ctDNA MRD for treatment personalization remains to be fully established. Here, we review the evidence supporting the value of ctDNA MRD in solid cancers and highlight key considerations in the application of this potentially transformative biomarker.
ctDNA analysis enables detection of MRD and predicts relapse after definitive treatment for solid cancers, thereby promising to revolutionize personalization of adjuvant and consolidation therapies.
越来越多的证据表明,治疗实体瘤后循环肿瘤 DNA(ctDNA)微小残留病灶(MRD)可预测复发。这些结果表明,ctDNA MRD 可以识别辅助治疗的候选者,并衡量此类治疗的反应。重要的是,检测类型、ctDNA 释放量、技术和生物学背景等因素会影响 ctDNA MRD 结果。此外,ctDNA MRD 用于治疗个体化的临床效用仍有待充分确立。在这里,我们回顾了支持 ctDNA MRD 在实体瘤中价值的证据,并强调了应用这种潜在变革性生物标志物的关键考虑因素。
ctDNA 分析可检测 MRD,并预测实体瘤确定性治疗后的复发,从而有望彻底改变辅助和巩固治疗的个体化。