Post‑operative urothelial recurrence in patients with upper urinary tract urothelial carcinoma managed by radical nephroureterectomy with an ipsilateral bladder cuff: Minimal prognostic impact in comparison with non‑urothelial recurrence and other clinical indicators
- Authors:
- Published online on: July 23, 2013 https://doi.org/10.3892/ol.2013.1485
- Pages: 1015-1020
Abstract
Introduction
Upper urinary tract urothelial carcinoma (UTUC) accounts for ~5% of all urothelial tumors and 10% of all renal tumors (1). Since the disease recurrence and progression rates are high in patients with UTUC (2), an improved understanding of the prognostic parameters may lead to the identification of patients who may benefit from intensified therapy and monitoring.
The classical risk factors for the development of UTUC include smoking, abuse of analgesics, chronic urinary tract infection, urolithiasis and oncological agents, such as cyclophosphamide (3). A significant prognostic factor of UTUC is the disease stage. The five-year survival rate for low stage tumors is ~90%, which decreases to <30% in cases of regional nodal metastases and to <10% in cases of distant metastases (4).
To date, several contemporary, single-center studies of patients who were treated with radical nephroureterectomy (RNU) for UTUC have been published (5–9), and several risk factors for developing UTUC have been reported, including a delay in the RNU (10) and tumor necrosis (11). Although the studies have largely contributed to our understanding of the disease, they were limited by small and heterogeneous populations. To overcome this limitation and to improve our understanding of the natural history of UTUC, a comprehensive database [the Upper Tract Urothelial Carcinoma Collaboration (UTUCC)] incorporating the clinicopathological characteristics and outcomes of >1,300 patients treated with RNU for UTUC at 13 academic centers worldwide was created in 2008 (12). It was concluded that an RNU provided durable local control and cancer-specific survival (CSS) in patients with a localized UTUC, and that the pathological tumor grade, T stage, lymph node status, tumor architecture and lymphovascular invasion (LVI) were significant prognostic variables that were associated with oncological outcomes, which may potentially be used to select patients for adjuvant systemic therapy.
However, there have been no studies that considered the prognostic value of urothelial recurrence in patients with UTUC of the kidney and ureter that is managed by surgery. Consequently, the present study focused on the prognostic impact of urothelial recurrence in comparison with non-urothelial recurrence.
Patients and methods
Patient selection
The present study was a retrospective analysis of 153 consecutive patients with UTUC, who underwent surgery between 1996 and 2009 at Hirakata City Hospital (Osaka, Japan). Of the 153 patients that were screened for the study, 103 patients were included in the analysis. The inclusion criteria consisted of a diagnosis of non-metastatic UTUC (any T stage, N0–1 and M0) and receipt of an RNU with an ipsilateral bladder cuff as the primary treatment. No patient had an invasive bladder tumor (BT) at the time of the RNU. Written informed consent was obtained from the patient. This study was approved by the ethics committee of Hirakata City Hospital (Osaka, Japan).
In the past, open RNU using an open excision of the distal ureter with a bladder cuff has been performed to dissect the kidney, with the entire length of the ureter and an adjacent segment of the bladder cuff. From June 2003 to date, the approach that has been used is one of conventional four-trocar nephrectomy. Once the nephrectomy is completed, the ureter is dissected and the intact specimen is moved into the pelvis. Next, a semi-Pfannenstiel incision is made in the lower abdomen, which assists in retrieving the specimen, eases the dissection of the lower ureter and facilitates the excision of the bladder cuff. The hilar and regional lymph nodes that are adjacent to the ipsilateral great vessel are then resected, if possible.
Study design
The following clinical and pathological variables were evaluated: Gender, age, tumor side, presence of a BT at diagnosis, serum level of C-reactive protein, hemoglobin, histological type, pathological grade, adjuvant chemotherapy, microvascular invasion, lymphatic invasion, urothelial recurrence, non-urothelial recurrence and pathological stage (2002 TNM system). The tumor grading was assessed according to the 1998 World Health Organization/International Society of Urologic Pathology consensus classification (13). All surgical specimens were processed according to the standard pathological procedures at the Hirakata City Hospital. UTUC was defined as a urothelial carcinoma located in the renal pelvis or calices, as well as tumors located within the ureter. C-reactive protein was pre-operatively obtained from the blood of the UTUC patients and collected in a serum-separating tube. The C-reactive protein level was expressed in units of mg/dl. Microvascular invasion was defined as tumor cells in an endothelium-lined space observed using routine light microscopy in whole-mounted UTUC specimens. The oncological follow-up schedule included a physical examination, cystoscopy and CT imaging between the chest and pelvis twice per year during the first five years and annually thereafter.
Statistical analysis
The continuous parametric variables were reported as mean ± SD and range. The continuous non-parametric variables were presented as median values and interquartile ranges. The F test was used to assess whether the standard deviations of two populations were equal. χ2 tests were conducted to assess the differences in the covariate distributions between the urothelial and non-urothelial recurrence categories. CSS was defined as the primary endpoint of the study. The survival interval was defined as the time elapsed between the surgery and the last clinical evaluation or cancer-specific mortality. Survival curves were estimated using the Kaplan-Meier method. The patients who remained alive or succumbed to other causes were censored. The log-rank test was used to compare the survival curves. A Cox proportional hazards regression model was used to verify the clinicopathological variables that independently predicted CSS. In all statistical analyses, a two-sided value of P<0.05 was considered to indicate a statistically significant difference. All data were analyzed using the PASW Statistics version 17 statistical program (SPSS Japan Inc., Tokyo, Japan).
Results
A total of 103 patients with comprehensive clinicopathological data, who fulfilled the inclusion criteria, were included in the analysis (Table I). The mean age was 68.6 years (interquartile range, 62–75 years). During the follow-up period, 45 patients (43.7%) succumbed to UTUC, 12 (11.7%) succumbed to other causes and 38 (36.9%) displayed evidence of disease recurrence. The median follow-up period for the surviving patients was 29 months (interquartile range, 14–63 months). The tumor was located on the right side in 55 patients (53.4%) and on the left side in 48 (46.6%). A BT was identified at the time of the UTUC diagnosis in 28 patients (27.2%). The histological type was urothelial in 92 patients (89.3%) and non-urothelial in 11 (10.7%). The pathological stage was divided into three groups: Superficial (pT0/pTis/pTa/pT1), muscle-invasive (pT2) and non-organ confined (pT3/pT4), which were identified in 43 (41.8%), 13 (12.6%) and 47 (45.6%) patients, respectively.
Table IClinicopathological characteristics grouped by non-urothelial or urothelial recurrence in 103 patients treated with an RNU and ipsilateral bladder cuff for UTUC. |
The median ages of the patients at the time of the surgery in the groups with non-urothelial recurrence (n=32) and without non-urothelial recurrence (n=71) were 70.5 and 69 years, respectively. The median ages in the groups with urothelial recurrence (n=38) and without urothelial recurrence (n=65) were 69 and 71 years, respectively. When comparing the risk parameters between the non-urothelial recurrence categories, the factors of pathological grade, microvascular invasion, lymphatic invasion and pT classification demonstrated significant differences. However, there were no significant differences observed between the urothelial recurrence categories.
The OS and CSS times between the urothelial recurrence categories showed no significant differences (P=0.3955 and P=0.05891, respectively), while a significant difference was observed within the non-urothelial recurrence categories (P<0.0001 and P<0.0001, respectively; Figs. 1–4).
The univariate analyses using the clinicopathological characteristics, including C-reactive protein, hemoglobin, pathological grade, non-urothelial recurrence, microvascular invasion, lymphatic invasion and pT classification, were associated with the CSS. In the multivariate analysis for the clinicopathological characteristics, only non-urothelial recurrence was associated with a worse CSS (P=0.002, HR 9.512; Table II).
Table IIUnivariate and multivariate Cox regression models for clinicopathological characteristics predicting CSS in 103 patients treated with RNU and ipsilateral bladder cuff for UTUC. |
Discussion
UTUC is a relatively rare malignancy. Although affected patients may benefit from endoscopic or nephron-sparing approaches, an RNU with an ipsilateral bladder cuff excision remains the standard treatment for patients with large, multifocal or high-grade tumors. However, despite definitive surgery, UTUC remains a malignancy with a high potential for local and distant recurrence, particularly in patients with advanced diseases (14). The outcomes of patients with UTUC following an RNU are heterogeneous and, therefore, difficult to predict. Multi-institutional collaborative studies have identified several potential factors that predict the outcome following an RNU for UTUC, supplementing the traditional pathological staging system (15–17).
Certain papers have examined the prognostic value of urothelial recurrence (particularly intravesical recurrence) following the treatment of an RNU for UTUC. Koda et al reported that intravesical recurrence following surgery for UTUC was not associated with the mode of surgery (i.e. laparoscopy-assisted or open surgery), and that the only risk factor for intravesical recurrence was a history of bladder cancer (18). Several other studies reported that it may be important to perform careful follow-up appointments that target intravesical recurrence for patients, particularly males and those with low-stage tumors and/or multifocal tumors, following RNU (19, 20). Concomitant carcinoma in situ (CIS) and the tumor size were predictors for bladder cancer recurrence (21). In a series of 196 patients, bladder recurrence was lower in those who received mitomycin C or epirubicin compared with those who did not received anything (29.0, 25.9 and 41.3%, respectively) (22). Novara et al observed that only a history of bladder cancer prior to an RNU was an independent risk factor for metachronous recurrence, which was identified in 6% of patients (23). Youssef et al underlined the prognostic impact of previous bladder cancer (24); patients with a positive bladder cancer (CIS) history had a greater risk of recurrence and mortality from UTUC following RNU (24).
The common locations for the spread of UTUC, depending on the site of the primary tumor, include para-aortic, paracaval, ipsilateral common iliac and pelvic lymph nodes. Hematogenous seeding also occurs in the liver, lungs and bone, which are common sites for metastases. Once a distant metastasis is diagnosed, the prognosis for the patient is extremely poor, in spite of chemotherapy. Certain publications suggest a benefit from the surgical removal of urothelial carcinoma metastases for a subgroup of patients (25). In a large German retrospective study, only 44 patients with distant metastases of the bladder or upper urinary tract underwent a complete resection of all the detectable metastases and were analyzed. The resected metastatic sites included the retroperitoneal lymph nodes (56.8%), distant lymph nodes (11.3%), lung (18.2%), bone (4.5%), adrenal gland (2.3%), brain (2.3%), small intestine (2.3%) and skin (2.3%). Pre- and/or post-metastasectomy systemic chemotherapy was administered in 35 of 44 patients (79.5%). Since no significant prognostic factors were determined due to the limited patient numbers, it was concluded that the metastasectomy in the patients with disseminated urothelial carcinoma metastases remained investigational and there are a limited number of disease types for which a combined-modality approach with systemic chemotherapy would be successful (26).
Lymph node dissection (LND) appears to have an impact on node-positive patients (27). In one previous study, 76 out of 293 patients developed disease relapse. Regional lymph node recurrence was the most common type of relapse (34 patients). In the multivariate analyses that adjusted for the effect of tumor stage and grade, pNx (skipping LND) was an adverse factor for locoregional recurrence and distant relapse (28). However, in the study by Lughezzani et al, which analyzed 2,824 patients from the Surveillance, Epidemiology and End Results (SEER) database, LND showed no benefit in patients with an N0 status compared with those with an Nx status (29). Roscigno et al suggested that LND should be performed in patients with suspected T2–4 stage diseases, to improve the prediction of the natural history of surgically treated UTUC and to use this information for possible adjuvant chemotherapy (30). Thus, the method of defining the right patient, LND template and the extent of the LND remains unclear.
The present study examined the prognostic value of urothelial and non-urothelial recurrence in patients with UTUC of the kidney and ureter that was managed by surgery. The OS and CSS times between the urothelial recurrence categories showed no significant differences, while significant differences were observed in the OS and CSS between the non-urothelial recurrence categories. The factors of pathological grade, microvascular invasion, lymphatic invasion and pT classification significantly affected the non-urothelial recurrence. However, no factors were observed to significantly affect the urothelial recurrence. In the multivariate analysis for clinicopathological characteristics, only non-urothelial recurrence remained associated with a worse CSS. The present data are limited by the retrospective nature of the study and the relatively small cohort. Prospective studies are required to confirm these findings. However, it may be concluded that non-urothelial recurrence significantly affected the prognosis in patients with UTUC managed by RNU with an ipsilateral bladder cuff compared with those with urothelial recurrence. The findings of the present study underscore the requirement for the careful follow-up and management of urothelial recurrence in patients with UTUC managed by RNU, which aids in lowering the risk of mortality due to cancer.
References
Jemal A, Siegel R, Xu J and Ward E: Cancer statistics, 2010. CA Cancer J Clin. 60:277–300. 2010. View Article : Google Scholar | |
Margulis V, Youssef RF, Karakiewicz PI, et al; Upper Tract Urothelial Carcinoma Group. Preoperative multivariable prognostic model for prediction of nonorgan confined urothelial carcinoma of the upper urinary tract. J Urol. 184:453–458. 2010. View Article : Google Scholar : PubMed/NCBI | |
Oosterlinck W, Solsona E, van der Meijden AP, et al; European Association of Urology. EAU guidelines on diagnosis and treatment of upper urinary tract transitional cell carcinoma. Eur Urol. 46:147–154. 2004. View Article : Google Scholar : PubMed/NCBI | |
Raman JD and Scherr DS: Management of patients with upper urinary tract transitional cell carcinoma. Nat Clin Pract Urol. 4:432–443. 2007. View Article : Google Scholar : PubMed/NCBI | |
Hall MC, Womack S, Sagalowsky AI, Carmody T, Erickstad MD and Roehrborn CG: Prognostic factors, recurrence, and survival in transitional cell carcinoma of the upper urinary tract: a 30-year experience in 252 patients. Urology. 52:594–601. 1998.PubMed/NCBI | |
Langner C, Hutterer G, Chromecki T, Winkelmayer I, Rehak P and Zigeuner R: pT classification, grade, and vascular invasion as prognostic indicators in urothelial carcinoma of the upper urinary tract. Mod Pathol. 19:272–279. 2006. View Article : Google Scholar : PubMed/NCBI | |
Novara G, De Marco V, Gottardo F, et al: Independent predictors of cancer-specific survival in transitional cell carcinoma of the upper urinary tract: multi-institutional dataset from 3 European centers. Cancer. 110:1715–1722. 2007. View Article : Google Scholar | |
Secin FP, Koppie TM, Salamanca JI, et al: Evaluation of regional lymph node dissection in patients with upper urinary tract urothelial cancer. Int J Urol. 14:26–32. 2007. View Article : Google Scholar : PubMed/NCBI | |
Brown GA, Busby JE, Wood CG, et al: Nephroureterectomy for treating upper urinary tract transitional cell carcinoma: Time to change the treatment paradigm? BJU Int. 98:1176–1180. 2006. View Article : Google Scholar : PubMed/NCBI | |
Waldert M, Karakiewicz PI, Raman JD, et al: A delay in radical nephroureterectomy can lead to upstaging. BJU Int. 105:812–817. 2010. View Article : Google Scholar : PubMed/NCBI | |
Zigeuner R, Shariat SF, Margulis V, et al: Tumour necrosis is an indicator of aggressive biology in patients with urothelial carcinoma of the upper urinary tract. Eur Urol. 57:575–581. 2010. View Article : Google Scholar : PubMed/NCBI | |
Margulis V, Shariat SF, Matin SF, et al; The Upper Tract Urothelial Carcinoma Collaboration. Outcomes of radical nephroureterectomy: a series from the Upper Tract Urothelial Carcinoma Collaboration. Cancer. 115:1224–1233. 2009. View Article : Google Scholar : PubMed/NCBI | |
Epstein JI, Amin MB, Reuter VR and Mostofi FK: The World Health Organization/International Society of Urological Pathology consensus classification of urothelial (transitional cell) neoplasms of the urinary bladder. Bladder Consensus Conference Committee. Am J Surg Pathol. 22:1435–1448. 1998. View Article : Google Scholar | |
Eng MK and Shalhav AL: Laparoscopic nephroureterectomy: long-term outcomes. Curr Opin Urol. 18:157–162. 2008. View Article : Google Scholar : PubMed/NCBI | |
Kikuchi E, Margulis V, Karakiewicz PI, et al: Lymphovascular invasion predicts clinical outcomes in patients with node-negative upper tract urothelial carcinoma. J Clin Oncol. 27:612–618. 2009. View Article : Google Scholar : PubMed/NCBI | |
Remzi M, Haitel A, Margulis V, et al: Tumour architecture is an independent predictor of outcomes after nephroureterectomy: a multi-institutional analysis of 1363 patients. BJU Int. 103:307–311. 2009. View Article : Google Scholar : PubMed/NCBI | |
Otto W, Shariat SF, Fritsche HM, et al: Concomitant carcinoma in situ as an independent prognostic parameter for recurrence and survival in upper tract urothelial carcinoma: a multicenter analysis of 772 patients. World J Urol. 29:487–494. 2011. View Article : Google Scholar : PubMed/NCBI | |
Koda S, Mita K, Shigeta M and Usui T: Risk factors for intravesical recurrence following urothelial carcinoma of the upper urinary tract: no relationship to the mode of surgery. Jpn J Clin Oncol. 37:296–301. 2007. View Article : Google Scholar : PubMed/NCBI | |
Kusuda Y, Miyake H, Terakawa T, Kondo Y, Miura T and Fujisawa M: Gender as a significant predictor of intravesical recurrence in patients with urothelial carcinoma of the upper urinary tract following nephroureterectomy. Urol Oncol. Aug 6–2011.(Epub ahead of print). | |
Terakawa T, Miyake H, Muramaki M, Takenaka A, Hara I and Fujisawa M: Risk factors for intravesical recurrence after surgical management of transitional cell carcinoma of the upper urinary tract. Urology. 71:123–127. 2008. View Article : Google Scholar : PubMed/NCBI | |
Pieras E, Frontera G, Ruiz X, Vicens A, Ozonas M and Pizá P: Concomitant carcinoma in situ and tumour size are prognostic factors for bladder recurrence after nephroureterectomy for upper tract transitional cell carcinoma. BJU Int. 106:1319–1323. 2010. View Article : Google Scholar | |
Wu WJ, Ke HL, Yang YH, Li CC, Chou YH and Huang CH: Should patients with primary upper urinary tract cancer receive prophylactic intravesical chemotherapy after nephroureterectomy? J Urol. 183:56–61. 2010. View Article : Google Scholar | |
Novara G, De Marco V, Dalpiaz O, et al: Independent predictors of contralateral metachronous upper urinary tract transitional cell carcinoma after nephroureterectomy: multi-institutional dataset from three European centers. Int J Urol. 16:187–191. 2009. View Article : Google Scholar | |
Youssef RF, Shariat SF, Lotan Y, et al: Prognostic effect of urinary bladder carcinoma in situ on clinical outcome of subsequent upper tract urothelial carcinoma. Urology. 77:861–866. 2011. View Article : Google Scholar : PubMed/NCBI | |
Remzi M, Shariat S, Huebner W, Fajkovic H and Seitz C: Upper urinary tract urothelial carcinoma: what have we learned in the last 4 years? Ther Adv Urol. 3:69–80. 2011.PubMed/NCBI | |
Lehmann J, Suttmann H, Albers P, et al: Surgery for metastatic urothelial carcinoma with curative intent: the German experience (AUO AB 30/05). Eur Urol. 55:1293–1299. 2009. View Article : Google Scholar : PubMed/NCBI | |
Bolenz C, Shariat SF, Fernández MI, et al: Risk stratification of patients with nodal involvement in upper tract urothelial carcinoma: value of lymph-node density. BJU Int. 103:302–306. 2009. View Article : Google Scholar : PubMed/NCBI | |
Abe T, Shinohara N, Muranaka M, et al: Role of lymph node dissection in the treatment of urothelial carcinoma of the upper urinary tract: multi-institutional relapse analysis and immunohistochemical re-evaluation of negative lymph nodes. Eur J Surg Oncol. 36:1085–1091. 2010. View Article : Google Scholar : PubMed/NCBI | |
Lughezzani G, Jeldres C, Isbarn H, et al: A critical appraisal of the value of lymph node dissection at nephroureterectomy for upper tract urothelial carcinoma. Urology. 75:118–124. 2010. View Article : Google Scholar : PubMed/NCBI | |
Roscigno M, Shariat SF, Margulis V, et al: Impact of lymph node dissection on cancer specific survival in patients with upper tract urothelial carcinoma treated with radical nephroureterectomy. J Urol. 181:2482–2489. 2009. View Article : Google Scholar : PubMed/NCBI |