Liquid Biopsy: Current advancements in clinical practice for bladder cancer

Felice Crocetto , Ugo Amicuzi , Michele Musone , Marco Magliocchetti , Dario Di Lieto , Simone Tammaro , Antonio Luigi Pastore , Andrea Fuschi , Roberto Falabella , Matteo Ferro , Roberto Bianchi , Marco Finati , Gian Maria Busetto , Giuseppe Lucarelli , Francesco Del giudice , Vincenzo Francesco Caputo , Raffaele Balsamo , Daniela Terracciano
{"title":"Liquid Biopsy: Current advancements in clinical practice for bladder cancer","authors":"Felice Crocetto ,&nbsp;Ugo Amicuzi ,&nbsp;Michele Musone ,&nbsp;Marco Magliocchetti ,&nbsp;Dario Di Lieto ,&nbsp;Simone Tammaro ,&nbsp;Antonio Luigi Pastore ,&nbsp;Andrea Fuschi ,&nbsp;Roberto Falabella ,&nbsp;Matteo Ferro ,&nbsp;Roberto Bianchi ,&nbsp;Marco Finati ,&nbsp;Gian Maria Busetto ,&nbsp;Giuseppe Lucarelli ,&nbsp;Francesco Del giudice ,&nbsp;Vincenzo Francesco Caputo ,&nbsp;Raffaele Balsamo ,&nbsp;Daniela Terracciano","doi":"10.1016/j.jlb.2025.100310","DOIUrl":null,"url":null,"abstract":"<div><div>Bladder cancer is the ninth most common malignancy worldwide, with two clinically distinct forms: non-muscle-invasive disease, characterized by high recurrence and excellent long-term survival, and muscle-invasive disease, associated with poorer outcomes. Current surveillance—cystoscopy and urine cytology—offers high specificity but is invasive, costly, and insensitive to low-grade tumors, underscoring the need for reliable, non-invasive biomarkers. Liquid biopsy approaches in urine and blood have demonstrated promise for real-time assessment of tumor burden, molecular heterogeneity, and early recurrence. Circulating tumor DNA (ctDNA) assays detect tumor-derived genetic and epigenetic alterations, enabling dynamic monitoring of minimal residual disease and treatment response. Methylation-based tests and CpG-targeted sequencing in urine achieve high diagnostic accuracy, potentially reducing dependence on cystoscopy. Molecular classification of bladder tumors into luminal and basal subtypes has refined therapeutic strategies: FGFR inhibitors for luminal-papillary tumors, EGFR-targeted and chemotherapy approaches for basal/squamous cases, and immune-checkpoint inhibitors guided by immune-infiltration profiles. Integration of artificial intelligence with multi-omic liquid biopsy data further enhances predictive modeling for recurrence, treatment response, and minimal residual disease detection. Despite these advances, clinical implementation faces challenges including pre-analytical variability, lack of standardized assays, limited prospective validation, and unclear cost-effectiveness. Harmonized protocols, large multicenter trials, and health-economic evaluations are essential to translate liquid biopsy technologies into routine practice. Future integration with advanced imaging, tissue biopsy, and digital pathology—supported by multidisciplinary collaboration and formal guideline endorsement—holds the potential to personalize bladder cancer management, reduce invasive procedures, and improve patient outcomes.</div></div>","PeriodicalId":101235,"journal":{"name":"The Journal of Liquid Biopsy","volume":"9 ","pages":"Article 100310"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Liquid Biopsy","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950195425000268","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Bladder cancer is the ninth most common malignancy worldwide, with two clinically distinct forms: non-muscle-invasive disease, characterized by high recurrence and excellent long-term survival, and muscle-invasive disease, associated with poorer outcomes. Current surveillance—cystoscopy and urine cytology—offers high specificity but is invasive, costly, and insensitive to low-grade tumors, underscoring the need for reliable, non-invasive biomarkers. Liquid biopsy approaches in urine and blood have demonstrated promise for real-time assessment of tumor burden, molecular heterogeneity, and early recurrence. Circulating tumor DNA (ctDNA) assays detect tumor-derived genetic and epigenetic alterations, enabling dynamic monitoring of minimal residual disease and treatment response. Methylation-based tests and CpG-targeted sequencing in urine achieve high diagnostic accuracy, potentially reducing dependence on cystoscopy. Molecular classification of bladder tumors into luminal and basal subtypes has refined therapeutic strategies: FGFR inhibitors for luminal-papillary tumors, EGFR-targeted and chemotherapy approaches for basal/squamous cases, and immune-checkpoint inhibitors guided by immune-infiltration profiles. Integration of artificial intelligence with multi-omic liquid biopsy data further enhances predictive modeling for recurrence, treatment response, and minimal residual disease detection. Despite these advances, clinical implementation faces challenges including pre-analytical variability, lack of standardized assays, limited prospective validation, and unclear cost-effectiveness. Harmonized protocols, large multicenter trials, and health-economic evaluations are essential to translate liquid biopsy technologies into routine practice. Future integration with advanced imaging, tissue biopsy, and digital pathology—supported by multidisciplinary collaboration and formal guideline endorsement—holds the potential to personalize bladder cancer management, reduce invasive procedures, and improve patient outcomes.
液体活检:膀胱癌临床实践的最新进展
膀胱癌是全球第九大最常见的恶性肿瘤,临床上有两种不同的形式:非肌肉侵袭性疾病,其特点是高复发率和良好的长期生存率,以及肌肉侵袭性疾病,其预后较差。目前的监测-膀胱镜检查和尿液细胞学-提供了高特异性,但是侵入性的,昂贵的,并且对低级别肿瘤不敏感,强调需要可靠的,非侵入性的生物标志物。尿液和血液中的液体活检方法已被证明有希望实时评估肿瘤负荷、分子异质性和早期复发。循环肿瘤DNA (ctDNA)检测检测肿瘤来源的遗传和表观遗传改变,从而能够动态监测最小残留疾病和治疗反应。基于甲基化的测试和尿液中cpg靶向测序具有很高的诊断准确性,潜在地减少了对膀胱镜检查的依赖。膀胱肿瘤分为管状和基底亚型的分子分类已经改进了治疗策略:用于光乳头状肿瘤的FGFR抑制剂,用于基底/鳞状病例的egfr靶向和化疗方法,以及由免疫浸润谱指导的免疫检查点抑制剂。人工智能与多组学液体活检数据的集成进一步增强了复发、治疗反应和最小残留疾病检测的预测建模。尽管取得了这些进展,但临床实施仍面临挑战,包括分析前变异性、缺乏标准化分析、有限的前瞻性验证和不明确的成本效益。统一的方案、大型多中心试验和健康经济评估对于将液体活检技术转化为常规实践至关重要。在多学科合作和正式指南认可的支持下,未来与先进成像、组织活检和数字病理学的整合,有可能实现膀胱癌个性化管理,减少侵入性手术,改善患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信