作者
Iver Nordentoft,Sia V. Lindskrog,Karin Birkenkamp‐Demtröder,Santiago González,Maja Kuzman,Jurica Levatić,Dunja Glavaš,Ryan Ptashkin,James B. Smadbeck,Danielle Afterman,Tomer Lauterman,Yarin Cohen,Zohar Donenhirsh,Iman Tavassoly,Ury Alon,Amanda Frydendahl,Mads Heilskov Rasmussen,Claus L. Andersen,Philippe Lamy,Michael Knudsen,Paz Polak,Asaf Zviran,Boris Oklander,Mads Agerbæk,Jørgen Bjerggaard Jensen,Lars Dyrskjøt
摘要
Circulating tumor DNA (ctDNA) can be used for sensitive detection of minimal residual disease (MRD). However, the probability of detecting ctDNA in settings of low tumor burden is limited by the number of mutations analyzed and the plasma volume available. We used a whole-genome sequencing (WGS) approach for ctDNA detection in patients with urothelial carcinoma.