术后持续盐水膀胱冲洗减少活跃的泌尿肿瘤细胞:一项NMIBC的前瞻性研究。

IF 4.8 2区 医学 Q2 CELL BIOLOGY
Cellular Oncology Pub Date : 2025-08-01 Epub Date: 2025-04-29 DOI:10.1007/s13402-025-01059-4
Qi Zhang, Yanhua Du, Dong Wang, Gan Du, Chuanzhen Cao, Xiaomin Yu, Xiaoli Zhang, Peipei Xie, Duo Wan, Li Wen, Hongzhe Shi, Youyan Guan, Li Lu, Xingang Bi, Shujun Cheng, Kaitai Zhang, Wen Zhang, Jianzhong Shou
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引用次数: 0

摘要

目的:TURBT联合即刻膀胱灌注后是否需要进一步的临床策略尚无临床证据。本研究旨在通过分析TURBT围手术期AUCC的变化,建立一种可靠的活动性尿癌细胞(AUCC)定量检测方法,探讨持续盐水膀胱灌洗(CSBI)作为一种可行选择的临床疗效。方法:采用单细胞全基因组测序法建立AUCC测定方法,并对其可靠性进行验证。2021 - 2023年,通过膀胱镜检查和病理活检确诊的膀胱癌患者(N = 324)和对照组(N = 92)纳入研究。入选的非肌肉浸润性膀胱癌(NMIBC)患者在接受CSBI或未接受CSBI后,分别接受TURBT和立即膀胱输注表阿霉素,并在术后第1天和第5天检测aucc。术后随访2年。结果:AUCC法具有较好的检测准确性,灵敏度为0.821,特异度为0.902。无论患者是否接受CSBI,在TURBT联合膀胱立即灌注后第一天,AUCC均升高。然而,在接受CSBI治疗的患者中,aucc在第5天下降得更快,并且伴有危险因素的患者从CSBI中获益更多。两年的随访结果显示,高危复杂手术患者可从CSBI中获益显著。结论:我们率先对AUCC进行了定量检测,并提供了实验室证据,证明TURBT可导致肿瘤细胞播散,而CSBI可作为降低潜在复发风险的进一步临床策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postoperative continuous saline bladder irrigation reduces active urinary cancer cells: a prospective study in NMIBC.

Purpose: There is a lack of clinical evidence on whether further clinical strategies are needed after TURBT combined with immediate bladder instillation. This study intends to establish a reliable quantitative assay for active urinary cancer cells (AUCC) and to investigate the clinical efficacy of continuous saline bladder irrigation (CSBI) as a feasible option by analyzing the perioperative AUCC changes in TURBT.

Methods: An AUCC assay was developed and its reliability was verified by single-cell whole genome sequencing. Bladder cancer patients (N = 324) diagnosed by cystoscopy and pathologic biopsy and control individuals (N = 92) were included from 2021 to 2023 in the study. Enrolled patients with non-muscle invasive bladder cancer (NMIBC) underwent TURBT followed by immediate bladder instillation of epirubicin, after subgroups received CSBI or not, and AUCCs were tested on the first and fifth postoperative day. The patients were followed up for two years for postoperative recurrence.

Results: The AUCC assay achieved good detection accuracy, with a sensitivity of 0.821 and specificity of 0.902. AUCC increased on the first day after TURBT in combination with immediate bladder instillation, regardless of whether or not the patient received CSBI. However, AUCCs decreased more rapidly on the fifth day in patients treated with CSBI, and patients with concomitant risk factors benefited more from CSBI. The two-year follow-up results showed that high-risk patients with complex surgeries could benefit significantly from CSBI.

Conclusions: We pioneered a quantitative assay for AUCC and provided laboratory evidence that TURBT causes tumor cell dissemination and CSBI can be a further clinical strategy to reduce the risk of potential recurrence.

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来源期刊
Cellular Oncology
Cellular Oncology ONCOLOGY-CELL BIOLOGY
CiteScore
10.30
自引率
1.50%
发文量
86
审稿时长
12 months
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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