Kast Richard E
IIAIGC Study Center, 11 Arlington Ct, Burlington, VT 05408, USA.
Biomedicines. 2025 Mar 13;13(3):706. doi: 10.3390/biomedicines13030706.
After it has metastasized, bladder cancer, the malignant transformation of the bladder urothelium, continues to be a common cause of death after maximal use of all currently available standard treatments. To address this problem in 2025, the drug repurposing movement within oncology aims to identify medicines in common general medical care use that have data indicating that they can interfere or inhibit a growth driving element that has been identified in bladder cancer. This paper now outlines extensive preclinical data showing that four drugs from general medical practice meet these criteria-the melatonergic drug ramelteon, the antidepressant fluoxetine, the antibiotic dapsone, and the analgesic drug celecoxib. This is the UBC4 regimen, meant as a possible adjunct added to standard treatments of metastatic bladder cancer. Three factors justify a clinical pilot trial of UBC4: (1) the UBC4 drugs are usually well tolerated and carry a low risk of harm, (2) the commonly fatal outcome of bladder cancer once it has widely metastasized, plus (3) the strong preclinical database showing UBC growth inhibition by each of the individual UBC4 drugs as outlined in this paper.
膀胱癌是膀胱尿路上皮的恶性转化,在发生转移后,即便最大限度地使用了所有现有的标准治疗方法,它仍是常见的致死原因。为解决这一问题,2025年肿瘤学领域的药物重新利用行动旨在从普通医疗常用药物中识别出有数据表明可干扰或抑制已在膀胱癌中确定的生长驱动因素的药物。本文现概述了大量临床前数据,表明来自普通医疗实践的四种药物符合这些标准,即褪黑素能药物雷美替胺、抗抑郁药氟西汀、抗生素氨苯砜和镇痛药塞来昔布。这就是UBC4方案,旨在作为转移性膀胱癌标准治疗的一种可能辅助手段。有三个因素支持对UBC4进行临床试点试验:(1)UBC4药物通常耐受性良好且危害风险低,(2)膀胱癌一旦广泛转移通常会导致致命后果,以及(3)如本文所述,强大的临床前数据库显示每种UBC4药物均可抑制UBC生长。