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循环肿瘤DNA在接受免疫检查点抑制剂治疗的恶性黑色素瘤患者中的预后价值:一项系统评价和荟萃分析。

The prognostic value of circulating tumor DNA in malignant melanoma patients treated with immune checkpoint inhibitors: a systematic review and meta-analysis.

作者信息

Liu Lei, Hou Shufu, Zhu Aiping, Yan Bing, Li Linchuan, Song Dandan

机构信息

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.

出版信息

Front Immunol. 2025 Jan 17;15:1520441. doi: 10.3389/fimmu.2024.1520441. eCollection 2024.

Abstract

BACKGROUND

Circulating tumor DNA (ctDNA) is an emerging biomarker in malignant melanoma(MM), and high levels of ctDNA may reflect a higher tumor load. However, its prognostic value for MM receiving immune checkpoint inhibitors(ICI) remains controversial. This meta-analysis aimed to elucidate the prognostic significance of ctDNA in this patient population.

METHODS

We conducted a comprehensive search of the PubMed, Cochrane Library, CNKI, and EMBASE databases, including studies published up to August 15, 2024, to investigate the prognostic impact of ctDNA in MM patients treated with ICI. Using a fixed-effects model, we systematically evaluated the association between ctDNA levels and key survival outcomes, including overall survival (OS) and progression-free survival (PFS). Additionally, funnel plots, Begg's test, and Egger's test were employed to assess potential publication bias.

RESULTS

Twelve studies from eleven articles, involving a total of 1063 eligible MM patients receiving ICI therapy, were included. The results indicated that patients with detectable ctDNA before initiating ICI therapy had significantly poorer OS (HR = 3.19, 95% CI = 2.22-4.58, P < 0.001) and PFS (HR = 2.08, 95% CI = 1.61-2.69, P < 0.001). Furthermore, the detectability of ctDNA during treatment was also significantly associated with worse OS (HR = 4.57, 95% CI = 3.03-6.91, P < 0.001) and PFS (HR = 3.79, 95% CI = 2.13-6.75, P < 0.001).

CONCLUSIONS

This meta-analysis indicates that in MM patients receiving ICI therapy, detectable and high levels of ctDNA are significantly associated with poorer OS and PFS. Therefore, ctDNA can serve as a diagnostic and stratification tool prior to treatment, as well as an effective indicator for monitoring treatment response and disease progression.

SYSTEMATIC REVIEW REGISTRATION

www.inplasy.com, identifier INPLASY2024110018.

摘要

背景

循环肿瘤DNA(ctDNA)是恶性黑色素瘤(MM)中一种新兴的生物标志物,高水平的ctDNA可能反映更高的肿瘤负荷。然而,其对接受免疫检查点抑制剂(ICI)治疗的MM患者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。

方法

我们全面检索了PubMed、Cochrane图书馆、中国知网和EMBASE数据库,包括截至2024年8月15日发表的研究,以调查ctDNA对接受ICI治疗的MM患者的预后影响。使用固定效应模型,我们系统地评估了ctDNA水平与关键生存结局之间的关联,包括总生存期(OS)和无进展生存期(PFS)。此外,采用漏斗图、Begg检验和Egger检验来评估潜在的发表偏倚。

结果

纳入了来自11篇文章的12项研究,共涉及1063例接受ICI治疗的符合条件的MM患者。结果表明,在开始ICI治疗前可检测到ctDNA的患者的OS(HR = 3.19,95%CI = 2.22 - 4.58,P < 0.001)和PFS(HR = 2.08,95%CI = 1.61 - 2.69,P < 0.001)显著较差。此外,治疗期间ctDNA的可检测性也与较差的OS(HR = 4.57,95%CI = 3.03 - 6.91,P < 0.001)和PFS(HR = 3.79,95%CI = 2.13 - 6.75,P < 0.001)显著相关。

结论

本荟萃分析表明,在接受ICI治疗的MM患者中,可检测到的高水平ctDNA与较差的OS和PFS显著相关。因此,ctDNA可作为治疗前的诊断和分层工具,以及监测治疗反应和疾病进展的有效指标。

系统评价注册

www.inplasy.com,标识符INPLASY2024110018。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b8/11782251/414d349dd770/fimmu-15-1520441-g001.jpg

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