» Articles » PMID: 39574043

The Effect of Circulating Tumor DNA on the Prognosis of Patients with Head and Neck Squamous Cell Carcinoma: a Systematic Review and Meta-analysis

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2024 Nov 22
PMID 39574043
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Circulating tumour DNA (ctDNA) has emerged as a valuable liquid biopsy biomarker in the field of oncology, including head and neck squamous cell carcinomas (HNSCCs), offering potential insights into cancer diagnosis, progression, and prognosis. This review aims to comprehensively evaluate the utility of ctDNA as a prognostic biomarker in HNSCC.

Methods: PubMed and Ovid were searched as part of our review. Studies that investigated the relationship between ctDNA and prognosis in HNSCC patients were included. Outcomes extracted included basic characteristics, ctDNA details and survival data. Meta-analysis was performed on eligible studies to determine pooled progression-free/recurrence-free survival (RFS/PFS) and overall survival (OS).

Results: Twenty-two studies were included, involving 5062 HNSCC patients from 11 countries. The meta-analysis demonstrated that the positive ctDNA/methylation detection was associated with worse OS (HR = 2.00, 95% CI 1.35-2.96) and worse PFS/RFS (HR = 3.54, 95% CI 1.05-11.85). Positive ctEBV DNA was associated with poorer OS (HR = 2.86, 95% CI 1.84-4.45) and poorer PFS/RFS (HR = 1.93, 95% CI 1.74-2.13). Positive ctHPV DNA was associated with poorer OS (HR = 1.38, 95% CI 1.07-1.38) but not PFS/PFS (HR = 1.33, 95% CI 0.96-1.85).

Conclusion: Meta-analysis indicates that the status of ctDNA is significantly associated with the prognosis of HNSCC patients, with ctDNA/methylation-negative patients demonstrating better PFS/RFS and OS.

References
1.
Rapado-Gonzalez O, Rodriguez-Ces A, Lopez-Lopez R, Suarez-Cunqueiro M . Liquid biopsies based on cell-free DNA as a potential biomarker in head and neck cancer. Jpn Dent Sci Rev. 2023; 59:289-302. PMC: 10480573. DOI: 10.1016/j.jdsr.2023.08.004. View

2.
Chan A, Hui E, Ngan R, Tung S, Cheng A, Ng W . Analysis of Plasma Epstein-Barr Virus DNA in Nasopharyngeal Cancer After Chemoradiation to Identify High-Risk Patients for Adjuvant Chemotherapy: A Randomized Controlled Trial. J Clin Oncol. 2018; :JCO2018777847. DOI: 10.1200/JCO.2018.77.7847. View

3.
Lam W, Chan K, Lo Y . Plasma Epstein-Barr virus DNA as an archetypal circulating tumour DNA marker. J Pathol. 2019; 247(5):641-649. PMC: 6594142. DOI: 10.1002/path.5249. View

4.
Wilson H, DAgostino Jr R, Meegalla N, Petro R, Commander S, Topaloglu U . The Prognostic and Therapeutic Value of the Mutational Profile of Blood and Tumor Tissue in Head and Neck Squamous Cell Carcinoma. Oncologist. 2020; 26(2):e279-e289. PMC: 7873320. DOI: 10.1002/onco.13573. View

5.
Cristiano S, Leal A, Phallen J, Fiksel J, Adleff V, Bruhm D . Genome-wide cell-free DNA fragmentation in patients with cancer. Nature. 2019; 570(7761):385-389. PMC: 6774252. DOI: 10.1038/s41586-019-1272-6. View