Zhao Xiumin, Hou Shufu, Hao Ruiqi, Zang Yelei, Song Dandan
Department of Neurology, Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Department of Gastrointestinal Surgery, Central Hospital Affiliated to Shandong First Medical University, Jinan, China.
Front Oncol. 2025 Apr 4;15:1566750. doi: 10.3389/fonc.2025.1566750. eCollection 2025.
Circulating tumor DNA (ctDNA) is an emerging biomarker in cervical cancer, with elevated levels typically indicating a higher tumor burden. However, its prognostic value in cervical cancer patients remains debated. This meta-analysis aims to clarify the prognostic significance of ctDNA in this patient population.
We searched the PubMed, Cochrane Library, CNKI, and EMBASE databases for studies published up to September 30, 2024, to investigate the prognostic significance of ctDNA in cervical cancer patients. The outcome measures included overall survival (OS) and progression-free survival (PFS)/disease-free survival (DFS).
This analysis included 10 studies encompassing a total of 706 cervical cancer patients. Findings revealed that patients with detectable baseline ctDNA had significantly poorer OS(HR = 1.64, 95% CI = 1.45-1.86, P < 0.001) as well as worse PFS or DFS (HR = 1.42, 95% CI = 1.07-1.89, P = 0.015). Additionally, ctDNA detectability during treatment was strongly associated with poorer OS (HR = 17.22, 95% CI = 4.43-66.89, P < 0.001) and PFS/DFS (HR = 4.16, 95% CI = 2.57-6.73, P < 0.001).
This meta-analysis demonstrates that elevated ctDNA levels are significantly associated with poorer PFS, DFS, and OS in patients with cervical cancer. However, data regarding the association between ctDNA levels and OS are relatively limited, and the number of included studies remains small, with a potential risk of publication bias. Based on the current evidence, ctDNA shows promise as a valuable tool for pre-treatment assessment and an effective biomarker for monitoring therapeutic response and disease progression. Further large-scale, prospective studies are warranted to validate these findings and establish their reliability and clinical applicability.
inplasy.com, identifier INPLASY2024120083.
循环肿瘤DNA(ctDNA)是宫颈癌中一种新兴的生物标志物,其水平升高通常表明肿瘤负荷较高。然而,其在宫颈癌患者中的预后价值仍存在争议。本荟萃分析旨在阐明ctDNA在该患者群体中的预后意义。
我们检索了截至2024年9月30日发表的PubMed、Cochrane图书馆、中国知网和EMBASE数据库,以研究ctDNA在宫颈癌患者中的预后意义。结局指标包括总生存期(OS)和无进展生存期(PFS)/无病生存期(DFS)。
本分析纳入了10项研究,共706例宫颈癌患者。研究结果显示,基线ctDNA可检测到的患者总生存期显著较差(HR = 1.64,95%CI = 1.45 - 1.86,P < 0.001),无进展生存期或无病生存期也较差(HR = 1.42,95%CI = 1.07 - 1.89,P = 0.015)。此外,治疗期间ctDNA的可检测性与较差的总生存期(HR = 17.22,95%CI = 4.43 - 66.89,P < 0.001)和无进展生存期/无病生存期(HR = 4.16,95%CI = 2.57 - 6.73,P < 0.001)密切相关。
本荟萃分析表明,ctDNA水平升高与宫颈癌患者较差的无进展生存期、无病生存期和总生存期显著相关。然而,关于ctDNA水平与总生存期之间关联的数据相对有限,纳入研究的数量仍然较少,存在潜在的发表偏倚风险。基于目前的证据,ctDNA有望成为一种有价值的治疗前评估工具以及监测治疗反应和疾病进展的有效生物标志物。需要进一步开展大规模的前瞻性研究来验证这些发现,并确定其可靠性和临床适用性。
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