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Prognostic utility of circulating tumor DNA methylation analysis in stage IV colorectal cancer.

Authors :
Momose H
Sugimoto K
Irie T
Nomura S
Ro H
Ishiyama S
Takahashi M
Pisanic T
Sakamoto K
Source :
Journal of surgical oncology [J Surg Oncol] 2024 Aug 19. Date of Electronic Publication: 2024 Aug 19.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Background and Objectives: Our aim in this study was to investigate the usefulness of circulating tumor (ct) DNA methylation analysis for predicting long-term outcomes after resection in Stage IV colorectal cancer (CRC).<br />Methods: Methylation analyses were performed on 95 plasma samples from patients with CRC who underwent surgery. The methylation status (relative methylation value: RMV) of CpG within the promoter region of three genes (CHFR, SOX11, and CDO1) was assessed to quantitative methylation-specific PCR (qMSP) analysis.<br />Results: In the patients who had undergone resection of the primary tumor and metastatic organs with curative intent, the CHFR-RMV high group had significantly worse recurrence-free survival (RFS) compared with the CHFR-RMV low group (p = 0.001). Multivariate analysis revealed that CHFR-RMV was a significant independent prognostic factor (hazard ratio = 2.63 (1.29-5.36); p = 0.008). In the patients who had undergone resection of the primary tumor with metastatic organs with curative intent after neoadjuvant systemic chemotherapy, the SOX11-RMV high group had significantly worse RFS compared with the SOX11-RMV low group (p = 0.004).<br />Conclusions: The current study showed the usefulness of ctDNA methylation analysis for predicting the possibility of curative resection and long-term outcomes after resection in Stage IV CRC. A future prospective study is needed to obtain more conclusive results.<br /> (© 2024 Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1096-9098
Database :
MEDLINE
Journal :
Journal of surgical oncology
Publication Type :
Academic Journal
Accession number :
39155651
Full Text :
https://doi.org/10.1002/jso.27824