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. Author manuscript; available in PMC: 2023 Jul 17.
Published in final edited form as: Clin Cancer Res. 2023 Jan 17;29(2):410–421. doi: 10.1158/1078-0432.CCR-22-1134

Figure 3. Longitudinal disease monitoring by sequencing of plasma-derived cfDNA samples from patients CD20 and CD26 with newly diagnosed endometrial cancer.

Figure 3.

A, Case CD20, B, Case CD26 with detectable pre-operative circulating tumor (ct) DNA and corresponding graphs of mutation allele frequencies (MAFs) according to the time of blood collection, treatment timeline and a pictographic representation of disease burden. MAFs of mutation in plasma DNA (left y-axis) extracted from peripheral blood samples obtained at baseline, post-surgery and serially every 6 months during follow-up, color-coded according to the legend. The ctDNA fraction (right y-axis) is shown by a dashed line. Below the graph, information about surgery, radiation therapy, chemotherapy, last follow-up, and schematic radiographic representations of disease burden are shown. AWD, alive with disease; DOD, dead of disease; EC, endometrial cancer; F/U, follow-up; MAF, mutant allele fraction.