Detection and Diagnostic Utilization of Cellular and Cell-Free Tumor DNA
Jonathan C. Dudley, Maximilian Diehn
Abstract
Because cancer is caused by an accumulation of genetic mutations, mutant DNA released by tumors can be used as a highly specific biomarker for cancer. Although this principle was described decades ago, the advent and falling costs of next-generation sequencing have made the use of tumor DNA as a biomarker increasingly practical. This review surveys the use of cellular and cell-free DNA for the detection of cancer, with a focus on recent technological developments and applications to solid tumors. It covers ( a) key principles and technology enabling the highly sensitive detection of tumor DNA; ( b) assessment of tumor DNA in plasma, including for genotyping, minimal residual disease detection, and early detection of localized cancer; ( c) detection of tumor DNA in body cavity fluids, such as urine or cerebrospinal fluid; and ( d) challenges posed to the use of tumor DNA as a biomarker by the phenomenon of benign clonal expansions.