Circulating Tumor DNA to Predict Radiographic and Pathologic Response to Total Neoadjuvant Therapy in Locally Advanced Rectal Cancer

被引:3
|
作者
Alden, Stephanie L. [1 ]
Lee, Valerie [2 ]
Narang, Amol K. [3 ]
Meyer, Jeffrey [3 ]
Gearhart, Susan L. [4 ]
Christenson, Eric S. [2 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD USA
[2] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Sch Med, Dept Oncol, Baltimore, MD USA
[3] Johns Hopkins Univ, Sidney Kimmel Canc Ctr Johns Hopkins, Sch Med, Dept Radiat Oncol & Mol Radiat Sci, Baltimore, MD USA
[4] Johns Hopkins Bayview Med Ctr, Dept Surg, Baltimore, MD USA
[5] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Dept Oncol, 1650 Orleans St,CRB1 Room 310, Baltimore, MD 21287 USA
关键词
circulating tumor DNA; rectal cancer; total neoadjuvant therapy; nonoperative management;
D O I
10.1093/oncolo/oyad336
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite advances in treatment and response assessment in locally advanced rectal cancer (LARC), it is unclear which patients should undergo nonoperative management (NOM). We performed a single-center, retrospective study to evaluate post-total neoadjuvant therapy (TNT) circulating tumor DNA (ctDNA) in predicting treatment response. We found that post-TNT ctDNA had a sensitivity of 23% and specificity of 100% for predicting residual disease upon resection, with a positive predictive value (PPV) of 100% and a negative predictive value (NPV) of 47%. For predicting poor tumor regression on MRI, ctDNA had a sensitivity of 16% and specificity of 96%, with a PPV of 75% and NPV of 60%. A commercially available ctDNA assay was insufficient to predict residual disease after TNT and should not be used alone to select patients for NOM in LARC. Despite advances in treatment and response assessment in locally advanced rectal cancer, it is unclear which patients should undergo nonoperative management. This article evaluates post-total neoadjuvant therapy circulating tumor DNA in predicting treatment response.
引用
收藏
页码:E414 / E418
页数:5
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