在疑似膀胱癌(血尿)的调查中,国家临床卓越研究所(NICE)指南是否应该取消尿液细胞学检查?

Madeline Moore, A. Robinson, M. Kitchen, L. Gommersall
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引用次数: 0

摘要

背景:尽管国家临床卓越研究所(NICE)的指南建议使用尿细胞学(UC)诊断膀胱癌,但其用途是可变的。造成这种情况的原因包括次优灵敏度、财务成本、可替代测试的可用性以及对结果解释的不确定性。然而,有趣的是,当其他检查正常时,可疑或恶性UC偶尔会导致癌症诊断。因此,我们回顾性评估了一组血尿患者,以确定UC在癌症诊断中的价值和非典型UC(分级为C3)的临床意义。患者和方法2015年,我们确定了3018例疑似癌症途径(“两周等待”)的血尿患者。我们回顾性分析了500例随机队列的临床、人口学和随访/结局数据。结果中位随访时间为58个月。500例患者中有61例诊断为泌尿系恶性肿瘤;所有患者均通过膀胱镜检查或影像学检查确定,即与UC结果无关。在5年随访期间,没有非典型UC再次出现“遗漏”癌症诊断的病例。然而,可疑和恶性细胞学与高级别/侵袭性肿瘤和随后的肿瘤复发有关。结论尿细胞学检查未发现影像学或膀胱镜检查未发现的肿瘤。血尿检查阴性的非典型UC似乎与恶性肿瘤无关,因此不应改变患者的管理,也不应提示进一步的调查。可疑和恶性UC与高风险癌症相关,因此可用于经尿道膀胱肿瘤切除术(turt)的优先等待名单,然而,尚不清楚这是否可能有利于患者的预后。因此,我们得出结论,UC在血尿调查中没有作用。
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Should National Institute for Clinical Excellence (NICE) Guidelines Remove Urine Cytology as a Suggested Adjunct in Suspected Bladder Cancer (haematuria) Investigations?
BackgroundDespite National Institute for Clinical Excellence (NICE) guidelines suggesting the use of urine cytology (UC) for the diagnosis of bladder cancer, its use is variable. Reasons for this include sub-optimal sensitivity, financial cost, availability of alternative tests, and uncertainty over interpretation of results. Anecdotally, however, suspicious or malignant UC when other investigations are normal, occasionally leads to a cancer diagnosis. Therefore, we retrospectively assessed a cohort of our haematuria patients to determine the value of UC in cancer diagnosis and the clinical significance of atypical UC (graded as C3). Patients and methodsWe identified 3018 patients with haematuria referred on the suspected cancer pathway (“two-week wait”) in 2015. We retrospectively analysed clinical, demographic, and follow-up/outcome data in a random cohort of 500 cases. ResultsMedian follow up was 58 months. Urological malignancy was diagnosed in 61/500 patients; all were identified by cystoscopy or imaging, i.e., irrespective of UC result. No cases of atypical UC re-presented with a ‘missed’ cancer diagnosis within the five-year follow-up period. However, suspicious and malignant cytology was associated with high-grade/aggressive tumours and subsequent tumour recurrence. ConclusionUrine cytology did not identify any cancers that were not already found by imaging or cystoscopy. Atypical UC in the presence of negative haematuria investigations does not appear to be associated with malignancy, and therefore should not alter patient management nor prompt further investigation. Suspicious and malignant UC was associated with higher risk cancers and could therefore be used to prioritise waiting lists for transurethral resection of bladder tumour (TURBT), however, it is unclear whether this might benefit patient outcomes. We conclude therefore that UC has no role in haematuria investigations.
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