Qu Feng, Darji Saloni, Thompson David H
Bindley Bioscience Center, Department of Chemistry, Multi-Disciplinary Cancer Research Facility, Purdue University, West Lafayette, IN 47907, USA.
Pharmaceutics. 2024 Aug 30;16(9):1154. doi: 10.3390/pharmaceutics16091154.
High-risk BCG-unresponsive non-muscle invasive bladder cancer (NMIBC) is a condition that is typically treated with Bacillus Calmette-Guérin (BCG) therapy. Unfortunately, NMIBC is characterized by high recurrence, with a significant percentage of BCG patients ultimately requiring radical cystectomy. As a consequence, the development of effective new therapies to avoid RC has become a rapidly evolving field to address this unmet clinical need. To date, three biologics-Keytruda, Adstiladrin, and Anktiva-have been approved by the FDA, and multiple drug modalities, particularly gene therapies, have shown promising results in clinical trials. Advances in drug delivery strategies, such as targeted delivery, sustained release, and permeabilization of protective layers, are critical in overcoming the challenges posed by therapeutic intervention in bladder cancer. This review focuses on high-risk BCG-unresponsive NMIBC therapies that have been or are currently being investigated in clinical trials, offering a broad overview of the delivery system designs and up-to-date clinical outcomes that have been reported as of July 2024. It aims to inform the development of future drug delivery systems for second-line therapies in high-risk BCG-unresponsive NMIBC.
高危卡介苗无反应性非肌肉浸润性膀胱癌(NMIBC)是一种通常采用卡介苗(BCG)疗法进行治疗的疾病。不幸的是,NMIBC的特点是复发率高,相当比例的BCG治疗患者最终需要进行根治性膀胱切除术。因此,开发有效的新疗法以避免进行根治性膀胱切除术已成为一个快速发展的领域,以满足这一未被满足的临床需求。迄今为止,三种生物制剂——可瑞达、Adstiladrin和Anktiva——已获得美国食品药品监督管理局(FDA)的批准,并且多种药物治疗方式,特别是基因疗法,在临床试验中显示出了有前景的结果。药物递送策略的进展,如靶向递送、缓释和保护层通透化,对于克服膀胱癌治疗干预所带来的挑战至关重要。本综述聚焦于已在或正在临床试验中研究的高危卡介苗无反应性NMIBC疗法,对截至2024年7月已报道的递送系统设计和最新临床结果进行了广泛概述。其目的是为高危卡介苗无反应性NMIBC二线治疗的未来药物递送系统的开发提供参考。