Noronha Mariana Macambira, da Silva Luís Felipe Leite, Almeida Luiz Felipe Costa, Passos Pedro Robson Costa, Reis Pedro Cotta Abrahão, Conrado João Evangelista Ponte, Filho Valbert Oliveira Costa, da Conceição Lucas Diniz, Ribeiro Mauricio F S A, Saibil Samuel D, Saldanha Erick F
Department of Medical Sciences, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil.
Department of Medical Sciences, Universidade Federal Fluminense, Niteroi, Rio de Janeiro, Brazil.
Pigment Cell Melanoma Res. 2025 Sep;38(5):e70047. doi: 10.1111/pcmr.70047.
Metastatic uveal melanoma (mUM) is a rare disease associated with poor prognosis and limited therapeutic options. Recent studies showed that detecting ctDNA is feasible and can aid treatment decisions for patients with mUM. We systematically searched PubMed, EMBASE, and Cochrane databases for eligible studies published up to May 2025 that included patients with mUM and reported data on the association between ctDNA and survival outcomes (OS and PFS). Statistical analyses were performed using Review Manager 5.4 software. Of the initial 450 records, seven studies met eligibility, including 518 patients with mUM. At baseline, ctDNA positivity was associated with significantly worse PFS (HR 2.34; 95% CI 1.56-3.51; p < 0.01; I = 0%) and OS (HR 3.32; 95% CI 2.09-5.29; p < 0.01; I = 48%). In patients treated with tebentafusp, ctDNA clearance was associated with superior OS (HR 0.19; 95% CI 0.07-0.49; p < 0.01; I = 46%) and any decrease in ctDNA was associated with better OS (HR 0.42; 95% CI 0.22-0.80; p < 0.01; I = 0%). This meta-analysis underscores ctDNA as a potential predictor of worse survival in patients with mUM, highlighting its potential to refine risk stratification and guide treatment strategies. Trial Registration: International Prospective Register of Systematic Reviews (PROSPERO): CRD42025638076.
转移性葡萄膜黑色素瘤(mUM)是一种罕见疾病,预后较差且治疗选择有限。最近的研究表明,检测循环肿瘤DNA(ctDNA)是可行的,并且可以帮助mUM患者做出治疗决策。我们系统检索了PubMed、EMBASE和Cochrane数据库,以查找截至2025年5月发表的符合条件的研究,这些研究纳入了mUM患者,并报告了ctDNA与生存结局(总生存期和无进展生存期)之间关联的数据。使用Review Manager 5.4软件进行统计分析。在最初的450条记录中,有7项研究符合纳入标准,包括518例mUM患者。在基线时,ctDNA阳性与显著更差的无进展生存期(风险比2.34;95%置信区间1.56 - 3.51;p < 0.01;异质性I = 0%)和总生存期(风险比3.32;95%置信区间2.09 - 5.29;p < 0.01;异质性I = 48%)相关。在接受替贝福司治疗的患者中,ctDNA清除与更好的总生存期相关(风险比0.19;95%置信区间0.07 - 0.49;p < 0.01;异质性I = 46%),并且ctDNA的任何下降都与更好的总生存期相关(风险比0.42;95%置信区间0.22 - 0.80;p < 0.01;异质性I = 0%)。这项荟萃分析强调ctDNA是mUM患者生存较差的潜在预测指标,突出了其在优化风险分层和指导治疗策略方面的潜力。试验注册:国际前瞻性系统评价注册库(PROSPERO):CRD42025638076。