8017 Background: Circulating tumor DNA (ctDNA) is a promising biomarker for detecting molecular residual disease (MRD) and predicting recurrence after curative treatment in non-small cell lung cancer (NSCLC). Ultrasensitive personalized assays have demonstrated clinical validity at detection thresholds of ~80-100 parts per million (PPM). As this assay can detect ctDNA at concentrations an order of magnitude lower (below 10 PPM), we extend these analyses to explore the clinical outcomes of patien
Clinical validity of ultrasensitive single-digit parts per million ctDNA detection in non–small cell lung cancer.
James R. Black·Robert Charles Swanton·Charles Abbott·Bailiang Li·Takahiro Karasaki·Alexander Azizi·Lydia Liu·Olivia Lucas·Charlotte Grieco·Aino‐Maija Leppä·Maise Al-Bakir·Wing Kin Liu·David Moore·Oliver Shutkever·Cian Murphy·Mariam Jamal-Hanjani·Rachel Marty Pyke·Sean Michael Boyle·Richard Chen·Jonathan Wan
