Hajdinjak Tine
Department of Urology, Maribor Teaching Hospital, Maribor, Slovenia.
Urol Oncol. 2008 Nov-Dec;26(6):646-51. doi: 10.1016/j.urolonc.2007.06.002. Epub 2008 Jan 15.
Since the introduction of the UroVysion test for detecting urothelial cancers in urine, its reported performance has varied. This article systematically analyzed reported results.
Articles in English conforming to the Oxford EBM criteria were included, with the evaluation focused on cancers that were histologically confirmed at the time of testing rather than on any cancers that might develop later. Where applicable, samples with no cells were reclassified as negative so as to further improve the actual estimation of test performance. Where available, cytology data were also analyzed. Meta-DiSc software was used for the statistical analyses.
We identified 14 studies involving 2477 FISH tests. The overall prevalence of urothelial cancers was 35%. The pooled sensitivity and specificity of all studies were 72% (69%-75%) and 83% (82%-85%), respectively. Cytology data were available from 12 studies, with the overall sensitivity and specificity being 42% (38%-45%) and 96% (95%-97%). Excluding Ta tumors, the sensitivity was 86% (82%-89%) for UroVysion and 61% (56%-66%) for cytology. The overall performance was higher for UroVysion than for cytology: diagnostic odds ratio, 16.8 and 14.1; AUC, 0.867 (SE 0.021) and 0.626 (SE 0.091). These differences in overall test performance measures almost disappeared when superficial cancer cases were excluded from the analysis.
The published trials suggest that for a general mix of cases, cytology results are highly specific. However, a negative cytology result does not meaningfully change the post-test probability of the presence of urothelial cancer. UroVysion FISH test results should not be considered to provide conclusive evidence for the presence or absence of urothelial cancer, but both positive and negative results do moderately influence the post-test probability of disease.
自尿液中检测尿路上皮癌的UroVysion检测方法问世以来,其报告的性能有所不同。本文系统分析了报告结果。
纳入符合牛津循证医学标准的英文文章,评估重点为检测时经组织学确诊的癌症,而非之后可能发生的任何癌症。在适用情况下,将无细胞样本重新分类为阴性,以进一步提高检测性能的实际估计。如有可用的细胞学数据,也进行分析。使用Meta-DiSc软件进行统计分析。
我们确定了14项研究,涉及2477次荧光原位杂交(FISH)检测。尿路上皮癌的总体患病率为35%。所有研究的合并敏感性和特异性分别为72%(69%-75%)和83%(82%-85%)。12项研究有细胞学数据,总体敏感性和特异性分别为42%(38%-45%)和96%(95%-97%)。排除Ta期肿瘤后,UroVysion检测的敏感性为86%(82%-89%),细胞学检测的敏感性为61%(56%-66%)。UroVysion检测的总体性能高于细胞学检测:诊断比值比分别为16.8和14.1;曲线下面积(AUC)分别为0.867(标准误0.021)和0.626(标准误0.091)。当分析中排除浅表癌病例时,这些总体检测性能指标的差异几乎消失。
已发表的试验表明,对于一般病例组合,细胞学结果具有高度特异性。然而,阴性细胞学结果并不能显著改变尿路上皮癌存在的检测后概率。UroVysion荧光原位杂交检测结果不应被视为提供尿路上皮癌存在与否的确凿证据,但阳性和阴性结果都会适度影响疾病的检测后概率。