E. Ococks,Alexander M. Frankell,N. Masque Soler,Nicola Grehan,Alex Northrop,H. M. T. Coles,Aisling M. Redmond,Ginny Devonshire,Jamie Weaver,Craig D. Hughes,Katie Lehovsky,A. Blasko,Barbara Nutzinger,Rebecca C. Fitzgerald,Elizabeth Smyth
The incidence of esophageal adenocarcinoma (EAC) is rapidly rising and has a 5-year survival rate of <20%. Beyond TNM (tumor-node-metastasis) staging, no reliable risk stratification tools exist and no large-scale studies have profiled circulating tumor DNA (ctDNA) at relapse in EAC. Here we analyze the prognostic potential of ctDNA dynamics in EAC, taking into account clonal hematopoiesis with indeterminate potential (CHIP).