Circulating tumor DNA and radiological tumor volume identify patients at risk for relapse with resected, early-stage non–small cell lung cancer
Menée à partir d'échantillons plasmatiques prélevés sur 117 patients atteints d'un cancer du poumon non à petites cellules de stade précoce traité par résection, cette étude met en évidence l'intérêt de l'ADN tumoral circulant et du volume tumoral radiologique pour identifier les patients présentant un risque de récidive
Background : Predicting relapse and overall survival in early-stage non-small cell lung cancer (NSCLC) patients remains challenging. Therefore, we hypothesized that detection of circulating tumor DNA (ctDNA) can identify patients with increased risk of relapse and that integrating radiological tumor volume measurement along with ctDNA detectability improves prediction of outcome.
Patients and Method : We analyzed 366 serial plasma samples from 85 patients who underwent surgical resections and assessed ctDNA using a next-generation sequencing liquid biopsy assay, and measured tumor volume using CT-based 3-dimensional annotation.
Results : Our results showed that patients with detectable ctDNA at baseline or after treatment and patients who did not clear ctDNA after treatment had a significantly worse clinical outcome. Integrating radiological analysis allowed the stratification in risk groups prognostic of clinical outcome as confirmed in an independent cohort of 32 patients.
Conclusions : Our findings suggest ctDNA and radiological monitoring could be valuable tools for guiding follow-up care and treatment decisions for early-stage NSCLC patients.
Annals of Oncology , article en libre accès, 2022