Urinary biomarkers for the diagnosis of urothelial bladder cancer

Jamie J. D'Costa , Douglas G. Ward , Richard T. Bryan
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引用次数: 3

Abstract

Urothelial bladder cancer is a common cancer associated with considerable burden for both patients and healthcare providers alike. The majority of patients present with non-muscle-invasive bladder cancer (NMIBC) which, although not immediately life-threatening, requires appropriate initial management and long-term surveillance which is both invasive and costly. Accurate diagnostic urinary biomarkers could be transformational in this setting, yet have proved to be a significant challenge to bladder cancer scientists over the last two decades. Such biomarkers would need to represent a range of tumour grades and stages, encompass inter- and intra-tumour heterogeneity, and compete with the current diagnostic gold standard of cystoscopy with a sensitivity and specificity of 85% and 87%, respectively. For the field to move forward in this current exciting era of high-throughput proteomics and genomics, bladder cancer scientists need to find a consensus on the optimal urinary substrate (DNA, RNA, protein, etc) and deliver robust well-designed studies in the correct populations with appropriate statistical input. Issues relating to tumour heterogeneity and anticipatory diagnosis also require considerable thought. The challenge remains unchanged.

尿路上皮性膀胱癌诊断的尿液生物标志物
尿路上皮性膀胱癌是一种常见的癌症,对患者和医疗保健提供者都有相当大的负担。大多数患者患有非肌肉浸润性膀胱癌(NMIBC),虽然不会立即危及生命,但需要适当的初始治疗和长期监测,这既具有侵入性又昂贵。在这种情况下,准确诊断尿液生物标志物可能具有变革性,但在过去二十年中,这已被证明是膀胱癌科学家面临的重大挑战。这样的生物标志物需要代表一系列肿瘤分级和分期,包括肿瘤间和肿瘤内的异质性,并与目前的膀胱镜诊断金标准竞争,其灵敏度和特异性分别为85%和87%。为了在这个令人兴奋的高通量蛋白质组学和基因组学时代向前发展,膀胱癌科学家需要在最佳尿液底物(DNA, RNA,蛋白质等)上找到共识,并在正确的人群中提供可靠的精心设计的研究,并提供适当的统计输入。与肿瘤异质性和预期诊断有关的问题也需要深思熟虑。挑战依然没有改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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