- Open Access
Diagnostic value of the UCA1 test for bladder cancer detection: a clinical study
© Milowich et al. 2015
- Received: 24 April 2015
- Accepted: 9 June 2015
- Published: 16 July 2015
To evaluate the efficiency of the UCA1 test as a diagnostic tool for the detection of bladder cancer.
Between October 2009 and December 2011 the UCA1 test was performed on collected urine samples from 162 patients divided into screening and follow-up groups, based on the absence or presence of prior bladder cancer. The test performance was then evaluated in each group and compared to cystoscopy and urinary cytology.
The overall sensitivity, specificity and positive and negative predictive values for the UCA1 test were 70, 70.7, 75.6 and 64.5%, respectively. We observed no difference in performance for tumours of higher grade or stage, but sensitivity was increased in the screening population compared to patients under follow-up (83.9 vs. 59%). The UCA1 test successfully detected all 7 cases of isolated carcinoma in situ and was more sensitive in this particular setting than cystoscopy or urinary cytology.
The efficiency of the UCA1 test for the detection of primary and recurring bladder cancer in our study was lower than previously reported. We confirmed the role of UCA1 as a possible adjunct to cystoscopy and cytology when a primary bladder cancer is suspected, but its role in the follow-up of recurring tumours remains limited. Further studies are needed to investigate the role of the UCA1 test in the early detection of carcinoma in situ lesions.
- UCA1 RNA, human
- Urothelial carcinoma associated 1
- Bladder cancer
- Urinary marker
Bladder cancer (BC) is the second most common urologic cancer. Although the majority of cases are diagnosed at early stages, up to 50% of tumours recur and 15–40% grow into muscle invasive disease (Amin et al. 2015). According to current guidelines, the diagnostic standard for BC is cystoscopy, often combined with urinary cytology (Kamat et al. 2013). This is also the approach used to follow-up patients with a history of BC. Though photodynamic diagnosis has improved the sensitivity of white cystoscopy for carcinoma in situ (CIS) lesions, both procedures remain invasive, time-consuming and costly, therefore making BC one of the most expensive malignancies to monitor and treat (Isfoss 2011; Van Rhijn et al. 2009). Cytology is a non-invasive test often performed on voided urine, with high specificity (96%) but low sensitivity (44%), particularly for low-grade tumours (Kamat et al. 2013). Several urine markers have been studied to help diagnose BC, and thereby decrease the need for cystoscopy as well as make following-up bladder cancer patients more cost-effective. To date, the Food and Drug Administration has approved six urine biomarkers for BC detection (Kamat et al. 2013; Tilki et al. 2011). Most markers have shown better sensitivity compared to cytology; however, their specificity remains lower (Tilki et al. 2011). None of those markers are currently recommended as standard diagnostic tools in routine urology (Kamat et al. 2013; Tilki et al. 2011).
Urothelial carcinoma associated 1 (UCA1) was recently identified as a non-coding RNA upregulated in BC compared to normal bladder tissues, and is thought to be involved in embryogenesis and in BC progression (Wang et al. 2006, 2008, 2012). Overexpression of UCA1 in the BLS-211 BC cell line significantly enhanced the tumorigenicity, invasion potential and drug resistance, both in vitro and in vivo (Wang et al. 2008). Yang et al. showed that UCA1 stimulates cell proliferation via the p300 coactivator CREB, through a PI3K-AKT dependent pathway (Yang et al. 2012). UCA1 was also identified as a very sensitive and specific urine marker of BC (Wang et al. 2006; Zhang et al. 2012; Srivastava et al. 2014). A recent study yielded a sensitivity of 79.49% and a specificity of 79.73%, suggesting that the UCA1 test could be used as an adjunct to cytology in early diagnosis of primary urinary BC (Srivastava et al. 2014). Those promising results motivated us to study the UCA1 test in an independent cohort, with a view to validating UCA1 as a reliable biomarker for BC detection. Instead of using fresh urine samples stored on ice, as previously described, we developed the UCA1 test on fixed urine samples in order to facilitate its use in daily practice (Wang et al. 2006). The test has been accredited (BELAC, ISO15189) since September 2009. The present work aims to report our experience regarding the clinical value of the UCA1 test when compared to routine diagnostic methods.
Patients demographics and baseline features
Overall patients (n = 161)
n = 79
n = 83
Age (median (range))
p < 0.00001
Urinary tract infection
p = 0.01
Benign prostatic hyperplasia
p = 0.004
p = 0.1
p = 0.09
p = 0.07
p = 0.0009
p = 0.24
Aristocholic acid nephropathy
p = 1
p = 1
p = 0.04
p = 0.09
p = 0.56
p = 0.56
Small cell carcinoma
Urine and tissue samples
Urine samples were collected in a tube containing 25 ml of the fixative solution Saccomanno™ (Prosan, Merelbeke, Belgium) and were delivered to the laboratory within 24 h. From these samples, 50 ml was used to conduct routine cytology. All cytological diagnoses were reviewed by a uropathologist (SR). Cytology was categorized as positive if cancer cells or cells with atypical changes suggesting malignancy were found, and as negative if normal cells or cells with inflammatory atypical changes were found.
In 96 patients, tissue samples were retrieved by biopsy, transurethral resection of the bladder (TURB) or surgical procedures. The histopathological diagnoses were reviewed by a uropathologist (SR).
Patients were divided into screening and follow-up groups, based on absence or presence of prior BC. Patients were considered disease-free if the workup was negative and no evidence of BC was found in the six following months. Patients with insufficient follow-up were excluded from the study. We evaluated the sensitivity, specificity, positive and negative predictive values of the UCA1 test in both patient groups compared to cystoscopy and cytology.
Among the 162 patients included in this study, 79 had no prior history of BC and 83 were part of the follow-up cohort. For each of these two groups, the breakdown between patients in terms of clinical features, cytology, cystoscopy and UCA1 test results is shown in Table 1. In all, 69 diagnoses of BC were made, of which 30 were primary BCs and 39 recurrent cases. Most cases (n = 65) were diagnosed as urothelial carcinomas, though two cases of pure squamous cell carcinoma and single cases of primary bladder adenocarcinoma and small cell carcinoma were also encountered. For 66 patients, no histological material was available and 65 of these patients were considered disease-free, as there was no suspicion of malignancy at the initial workup or during a follow-up of at least 6 months either. One patient was diagnosed with a locally advanced bladder tumour on imaging findings and malignant urothelial cells were identified by cytology, but no further investigations were carried out due to the patient’s age and performance status.
Sensitivity of diagnostic methods for bladder cancer (including carcinoma in situ) according to grade and stage
n = 69
n = 65
n = 23
n = 35
n = 7
Squamous cell carcinoma
n = 2
n = 1
Small cell carcinoma
n = 1
n = 21
n = 15
n = 26
The overall sensitivities of cytology, cystoscopy and the UCA1 test were 50.8, 79.1 and 70%. The sensitivity of the UCA1 test was higher in the screening group compared to the follow-up group, (83.9 vs. 59%), yielding a negative predictive value of 86.1 and 68% respectively. Cystoscopy and urinary cytology were also less sensitive for detecting recurrences, with cystoscopy remaining the most efficient procedure (90 and 70.3% sensitivity for screening and follow-up), while urinary cytology detected 71.4% of primary BCs and only 34.3% of recurrences. Conversely, the UCA1 test proved to be more specific in the follow-up group as compared to the screening group (77.3 vs. 64.6%), yielding a positive predictive value of 64.5% overall. The specificity of cystoscopy in the follow-up group was equivalent (77.3%) to the UCA1 test, but both cystoscopy and cytology were more specific than the UCA1 test in the screening setting.
Diagnostic value of the UCA1 test, urinary cytology and cystoscopy for the detection of bladder cancer
Negative predictive value
Positive predictive value
Negative predictive value
Positive predictive value
Negative predictive value
Positive predictive value
Since its first description in 2006, several studies have confirmed UCA1 to be a biomarker for urothelial carcinoma and studied its expression in other cancers, including colorectal and breast cancers (Wang et al. 2006, 2008, 2012; Yang et al. 2012; Zhang et al. 2012; Srivastava et al. 2014; Han et al. 2014; Huang et al. 2014). Moreover, long non-coding RNAs, like UCA1, are increasingly thought to play a pivotal role in cancer development and progression (Shi et al. 2013; Li and Chen 2013). To date, only three studies have addressed the role of UCA1 as a urinary marker. BC is the second most common urologic malignancy, yet it is one of the most challenging to treat due to significant tumour heterogeneity and potential life-long follow-up, which includes time-consuming and invasive procedures. The implementation of a urinary biomarker in clinical practice could allow for longer intervals between cystoscopies and a less invasive follow-up, but should not come at the expense of lower sensitivity.
In previous studies, the sensitivity of the UCA1 marker ranged from 79.5 to 88.5%. With an overall sensitivity of 70%, the ability of the UCA1 test to detect BC was significantly lower in our series. However, when limited to the screening group, the UCA1 test yielded a sensitivity of 83.9%, which is comparable to reported results. Two of the previous studies did not detail the patients’ history of BC, but Srivastava et al. reported a significant difference in expression of UCA1 in recurrent tumours compared to primary tumours (p < 0.001), emphasizing the necessity to analyse patients with recurrent BC separately when evaluating a novel biomarker (Srivastava et al. 2014). The positive and negative predictive values of the UCA1 test were lower than previously reported (64.5 and 75.6% respectively), despite a relatively high prevalence of bladder cancer in our patients population (Srivastava et al. 2014).
The overall specificity of the UCA1 test was 70.7%, ranging lower than the previously published results (79.7–92.3%). In our study, 27 patients with a positive UCA1 test had no evidence of disease for at least 6 months and up to 53 months of follow-up. Nevertheless, late recurrences have been reported, which provide reasonable explanations for false positive results with other urinary markers, particularly FISH-based markers (Kamat et al. 2014 Oct). Anticipatory false-positive findings cannot be excluded at this stage and overexpression of UCA1 may be due to its expression in early precursor lesions that remain clinically undetectable. This hypothesis is supported by the detection of UCA1 in all seven cases of CIS and, additionally, in two cases of urothelial dysplasia (data not shown). Though four patients with false-positive tests were under surveillance for BC due to exposure to aristocholic acid, and one patient had been diagnosed with chronic schistosomiasis—two conditions associated with urothelial carcinogenic ability and urothelial dysplasia –, we did not find any association between particular clinical features and a false-positive test (Botelho et al. 2011; Lemy et al. 2008). Our study included only seven patients with CIS, but it is interesting to note that the UCA1 test detected three additional cases compared to cystoscopy. However, in order to evaluate the efficiency of the UCA1 test in flat urothelial lesions, further studies on larger cohorts are necessary.
Contrary to previous reports where UCA1 has emerged as a particularly sensitive marker for superficial high-grade tumours, we did not find any significant difference in terms of sensitivity when the UCA1 test was analysed according to grade. Although the UCA1 test was particularly efficient in detecting pT1 tumours, the sensitivity for both non-invasive and muscle-invasive tumours was 57%.
UCA1 expression was increased in various urothelial neoplastic lesions, including urothelial dysplasia, CIS and papillary low-grade and high-grade urothelial carcinomas—each associated with different morphology, pathogenesis and prognostic implications. Increased expression of UCA1 has been associated with tumour proliferation, migration and invasion, though the exact mechanisms are yet to be elucidated. Recently, Wang et al. reported that UCA1 promotes cell growth by downregulating the cell cycle inhibitor p21 via BRG1, a chromatin remodelling factor with anti-tumour properties (Wang et al. 2014). Furthermore, upregulated UCA1 has been shown to promote resistance to cisplatin-based chemotherapy in bladder cancer cells (Fan et al. 2014). Taken together, these findings indicate that UCA1 plays an important role in BC pathogenesis and progression, while its characterisation may provide new insights in early stages of BC development and, possibly, even new prognostic factors and therapeutic targets. It remains to be proven whether UCA1 is a suitable diagnostic urinary biomarker in BC and a useful contribution to already existing diagnostic procedures in daily urologic practice.
In conclusion, the efficiency of the UCA1 test for the diagnosis of BC in our study was lower than previously reported. Our results highlight the importance of testing novel urinary biomarkers in specific patient populations. The UCA1 test cannot replace cystoscopy for the evaluation of patients with suspected primary BC or in the context of a follow-up for bladder cancer. While it may aid in the detection of CIS, more extensive studies are needed to confirm these findings. Conversely, our results did not provide evidence that the UCA1 test is suitable for the follow-up of patients with previous BC, due to its low sensitivity in this population.
The present study has been approved by the Ethical Committee of the Erasme University Hospital (Ref: P2010/338).
DM data collection, data analysis, manuscript writing. MLM project development, data analysis and manuscript writing/editing. NDN project development, data analysis. FS project development. TR manuscript editing. CD data analysis. IS project development. SR project development, data analysis and manuscript writing/editing. All authors read and approved the final manuscript.
This work has been carried out with the support of grants awarded by the “Fonds Yvonne Boël”, Brussels, Belgium. The CMMI is supported by the European Regional Development. Fund and Wallonia. C.D. is a Senior Research Associate with the FNRS. C.D. is a Senior Research Associate with the “Fond National de la Recherche Scientifique”, Brussels, Belgium.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.
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