Elmasri Meera, Clark Aaron, Grundy Luke
Flinders Health and Medical Research Institute (FHMRI), College of Medicine and Public Health, Flinders University, Adelaide 5042, Australia.
Brain Sci. 2024 Nov 28;14(12):1203. doi: 10.3390/brainsci14121203.
Non-muscle invasive bladder cancer (NMIBC) accounts for approximately 70-75% of all bladder cancer cases. The standard treatment for high-risk NMIBC involves transurethral tumour resection followed by intravesical Bacillus Calmette-Guerin (BCG) immunotherapy. While BCG immunotherapy is both safe and effective, it frequently leads to the development of lower urinary tract symptoms (LUTS) such as urinary urgency, frequency, dysuria, and pelvic discomfort. These symptoms can significantly diminish patients' quality of life and may result in the discontinuation of BCG treatment, adversely affecting oncological outcomes. Despite the considerable clinical impact of BCG-induced LUTS, the underlying mechanisms remain unclear, hindering the implementation or development of effective treatments. This review provides novel insights into the potential mechanisms underlying BCG-induced LUTS, focusing on the integrated roles of afferent and efferent nerves in both normal and pathological bladder sensation and function. Specifically, this review examines how the body's response to BCG-through the development of inflammation, increased urothelial permeability, and altered urothelial signalling-might contribute to LUTS development. Drawing from known mechanisms in other common urological disorders and data from successful clinical trials involving NMIBC patients, this review summarises evidence supporting the likely changes in both sensory nerve signalling and bladder muscle function in the development of BCG-induced LUTS. However, further research is required to understand the intricate mechanisms underlying the development of BCG-induced LUTS and identify why some patients are more likely to experience BCG intolerance. Addressing these knowledge gaps could have profound implications for patients' quality of life, treatment adherence, and overall outcomes in NMIBC care.
非肌层浸润性膀胱癌(NMIBC)约占所有膀胱癌病例的70-75%。高危NMIBC的标准治疗包括经尿道肿瘤切除术,随后进行膀胱内卡介苗(BCG)免疫治疗。虽然BCG免疫治疗既安全又有效,但它经常导致下尿路症状(LUTS)的出现,如尿急、尿频、尿痛和盆腔不适。这些症状会显著降低患者的生活质量,并可能导致BCG治疗中断,对肿瘤学结局产生不利影响。尽管BCG诱导的LUTS具有相当大的临床影响,但其潜在机制仍不清楚,这阻碍了有效治疗方法的实施或开发。本综述提供了关于BCG诱导的LUTS潜在机制的新见解,重点关注传入神经和传出神经在正常和病理性膀胱感觉及功能中的综合作用。具体而言,本综述探讨了机体对BCG的反应——通过炎症的发展、尿路上皮通透性增加和尿路上皮信号改变——可能如何导致LUTS的发生。借鉴其他常见泌尿系统疾病的已知机制以及涉及NMIBC患者的成功临床试验数据,本综述总结了支持BCG诱导的LUTS发生过程中感觉神经信号和膀胱肌肉功能可能发生变化的证据。然而,需要进一步研究以了解BCG诱导的LUTS发生的复杂机制,并确定为什么有些患者更容易出现BCG不耐受。填补这些知识空白可能对NMIBC护理中患者的生活质量、治疗依从性和总体结局产生深远影响。