Longitudinal ctDNA Monitoring for Postsurgical Disease Surveillance in Patients with Stage I to IIIB Melanoma

作者：G. Ansstas, Karam Khaddour, Sumedha Sudhaman, Karen Lin, Griffin Budde, A. Poklepovic, Bently P. Doonan, Meghan J. Mooradian, Ryan J. Sullivan, T. Vincent, Jeremy Rosiecki, Steven Y. Liu, Ronald Drengler, Daniel Blake Flora, Georgia M. Beasley, Kristen E. Rhodin, John Hyngstrom, Elise K. Brunsgaard, J. Bryce Ortiz, Giby V. George, Michael Krainock, Minetta C. Liu, Alan Tan · 发表于：Clinical Cancer Research · 年份：2026 · DOI：10.1158/1078-0432.ccr-25-3643 · 被引用次数：6 · 研究领域：Cancer Genomics and Diagnostics、Cancer Cells and Metastasis、Epigenetics and DNA Methylation

PURPOSE: Circulating tumor DNA (ctDNA) has emerged as an important biomarker for early recurrence detection and disease status monitoring during treatment in patients with cancer, including melanoma. We evaluate the prognostic value and impact of postoperative ctDNA detection in patients with stage I to IIIB melanoma using a clinically validated ctDNA assay. EXPERIMENTAL DESIGN: We conducted a retrospective analysis of real-world data of patients with stage I to IIIB melanoma, including ctDNA results using a personalized, tumor-informed, 16-plex multiplex PCR-next-generation sequencing assay. Adjuvant treatment decisions and postsurgical plasma sample collection timepoints were at the physician's discretion. ctDNA results were correlated with clinical outcomes. RESULTS: Across 190 patients and a total of 1,578 samples, a median of 7 ctDNA tests (range: 1-33) per patient were performed over a median period of 24.6 months (range: 3.7-74.7). ctDNA positivity at any postoperative timepoint was significantly associated with shorter recurrence-free survival [RFS; hazard ratio (HR): 40.63; 95% confidence interval (CI), 19.9-82.96; P < 0.0001). This finding was also observed in patients specifically with regional or distant recurrence (HR: 39.55; 95% CI, 18.08-86.51; P < 0.0001). In multivariate analysis, ctDNA positivity was the most significant prognostic factor associated with RFS when compared with other clinicopathologic factors, including stage, sex, and mitotic rate (HR: 25.36...