[类器官作为尿路上皮癌个性化治疗道路上的里程碑:系统回顾]。

Urologie (Heidelberg, Germany) Pub Date : 2022-07-01 Epub Date: 2022-06-13 DOI:10.1007/s00120-022-01854-z
Michael Karl Melzer, Viktor Zehe, Friedemann Zengerling, Felix Wezel, Cagatay Günes, Philipp Maisch, Christian Bolenz
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引用次数: 0

摘要

背景:局部晚期和转移性尿路上皮癌(UC)的治疗选择目前仅限于既定的化疗和免疫治疗方案。到目前为止,靶向治疗仅限于一小部分患者。尿路上皮类器官系统可以通过测试个体患者的敏感性来预测药物反应,从而在建立有效的个性化治疗方案方面做出决定性的贡献。本文的目的是描述UC临床应用类器官系统的科学现状。方法:在几个医学数据库(Medline, Cochrane Library)和研究注册(ClinicalTrials.gov, EU临床试验注册和WHO国际临床试验注册)中进行了系统的文献检索。根据所使用的数据库,对搜索词和搜索策略进行了调整。结果:总体而言,7项研究符合UC类器官主题的纳入标准。这些研究描述了在膀胱或肾盂肿瘤患者中建立类器官系统的基本工作流程。非肌肉浸润性膀胱癌生成类器官的成功率为70-77%,肌肉浸润性膀胱癌为42%。对患者类器官进行了系统的药物检测。结论:UC类器官的生成是可行的,个体治疗形式的离体试验是可能的。由于缺乏标准化的方法,它们的实施目前仍处于试验阶段。该方法具有很高的潜力,为尿路上皮癌患者提供个性化的治疗概念。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Organoids as a milestone on the way to personalized treatment of urothelial carcinoma: a systematic review].

Background: The treatment options for locally advanced and metastatic urothelial carcinoma (UC) are currently limited to established chemotherapy and immunotherapy protocols. Targeted treatment is so far restricted to a small subgroup of patients. Urothelial organoid systems could make a decisive contribution in establishing effective personalized treatment options by enabling drug response prediction through testing the sensitivity of individual patients. The aim of this article is to describe the state of the science of clinically applicable organoid systems for UC.

Methodology: A systematic literature search was conducted in several medical databases (Medline, Cochrane Library) and study registers (ClinicalTrials.gov, the EU Clinical Trials Register and the WHO International Clinical Trials Registry). The search terms and the search strategy were adapted to the databases used.

Results: Overall, 7 studies met the inclusion criteria on the topic of UC organoids. These studies describe the fundamental workflow in establishing organoid systems in patients with tumors of the urinary bladder or the renal pelvis. The success rates in generating organoids from non-muscle-invasive bladder cancer were 70-77% and for muscle-invasive bladder cancer 42%. For patient organoids systematic drug testing was carried out.

Conclusion: The generation of UC organoids is feasible and the ex vivo testing of individual treatment forms is possible. Due to the lack of a standardized methodology, their implementation remains experimental at the moment. The methodology has a high potential to provide a personalized treatment concept to patients with urothelial cancer.

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