Circulating Tumor DNA to Predict Radiographic and Pathologic Response to Total Neoadjuvant Therapy in Locally Advanced Rectal Cancer.
Stephanie L AldenValerie LeeAmol K NarangJeffrey MeyerSusan L GearhartEric S ChristensonPublished in: The oncologist (2024)
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.
Keyphrases
- circulating tumor
- locally advanced
- rectal cancer
- circulating tumor cells
- cell free
- neoadjuvant chemotherapy
- squamous cell carcinoma
- end stage renal disease
- radiation therapy
- newly diagnosed
- phase ii study
- ejection fraction
- chronic kidney disease
- prognostic factors
- peritoneal dialysis
- patient reported outcomes
- cell therapy
- computed tomography
- smoking cessation