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Radiotherapy may improve overall survival of patients with T3/T4 transitional cell carcinoma of the renal pelvis or ureter and delay bladder tumour relapse
© Chen et al; licensee BioMed Central Ltd. 2011
Received: 25 July 2010
Accepted: 14 July 2011
Published: 14 July 2011
Since transitional cell carcinoma (TCC) of the upper urinary tract is a relatively uncommon malignancy, the role of adjuvant radiotherapy is unknown.
We treated 133 patients with TCC of the renal pelvis or ureter at our institution between 1998 and 2008. The 67 patients who received external beam radiotherapy (EBRT) following surgery were assigned to the radiation group (RT). The clinical target volume included the renal fossa, the course of the ureter to the entire bladder, and the paracaval and para-aortic lymph nodes, which were at risk of harbouring metastatic disease in 53 patients. The tumour bed or residual tumour was targeted in 14 patients. The median radiation dose administered was 50 Gy. The 66 patients who received intravesical chemotherapy were assigned to the non-radiation group (non-RT).
The overall survival rates for the RT and non-RT groups were not significantly different (p = 0.198). However, there was a significant difference between the survival rates for these groups based on patients with T3/T4 stage cancer. A significant difference was observed in the bladder tumour relapse rate between the irradiated and non-irradiated bladder groups (p = 0.004). Multivariate analysis indicated that improved overall survival was associated with age < 60 years, T1 or T2 stage, absence of synchronous LN metastases, and EBRT. Acute gastrointestinal and bladder reactions were the most common symptoms, but mild non-severe (> grade 3) hematologic symptoms also occurred.
EBRT may improve overall survival for patients with T3/T4 cancer of the renal pelvis or ureter and delay bladder tumour recurrence in all patients.
Transitional cell carcinoma (TCC) of the renal pelvis and ureter is a relatively uncommon malignancy; it is estimated to account for 7% of all renal neoplasms and 5% of all urothelial malignancies in the United States . Upper urinary tract carcinoma is often a multifocal process, meaning that patients with cancer localised to the upper urinary tract are at greater risk of developing transitional tumours elsewhere. Approximately 20-50% of patients with an upper urinary tract tumour will develop bladder cancer [2–4].
Radical nephroureterectomy is a routine initial therapy for most patients with TCC of the renal pelvis or ureter. Surgery alone provides sufficient loco-regional control for the majority of patients that present with early stage disease; however, the overall 5-year survival rate after surgery ranges from 0-34% for patients with locally advanced TCC of the renal pelvis and ureter. The rate of local failure is reported to be between 30 and 50%, and this is the major cause of mortality in TCC patients [2–5].
The role of adjuvant external beam radiotherapy (EBRT) in the treatment of patients with TCC of the renal pelvis and ureter is unknown. Some studies report that EBRT is not effective; therefore, EBRT is not recommended for use as a prophylactic postoperative therapy [6, 7]. In contrast, other studies report that EBRT may improve the treatment outcome when it is concurrently administered with chemotherapy in patients with resected, locally advanced, upper tract urothelial malignancies. The ability of EBRT to improve the treatment outcome for patients with locally advanced renal pelvis or ureter cancer has been assessed [8, 9], but the studies included a small patient population and were not detailed enough to draw any conclusions. In this study, we report on a relatively large group of patients with TCC of the renal pelvis and ureter who were treated with postoperative radiotherapy and intravesical chemotherapy. Therefore, this study provides a detailed evaluation of the efficacy of adjuvant radiotherapy in patients with TCC of the renal pelvis and ureter.
Patients and staging evaluation
68.5 ± 1.430
66.2 ± 1.208
< 60 years
Pathologic T stage
Surgical resection: Before surgical resection, all patients were required to undergo computed tomography (CT) and/or magnetic resonance imaging (MRI) of the abdomen and pelvis, and an intravenous excretory urogram or retrograde pyelogram. Of the 133 patients in the study, 108 were treated with the standard approach of radical nephroureterectomy, including removal of the contents of Gerota's fascia with the ipsilateral ureter and the cuff of the bladder at its distal extent. Open nephron-sparing surgery for upper-tract TCC was used in patients with a large renal pelvic tumour in a single kidney. A partial ureterectomy or distal ureterectomy with reimplantation is a reasonable treatment alternative for patients who underwent palliative resection (R2, macroscopic residual) or had poor kidney function. Twenty-five patients underwent local resection surgery, including nine patients with gross lymph node metastases or accompanying cancers, for which palliative resection was subsequently performed. There were five patients over 80 years of age, four patients with poor kidney function or an absent contralateral kidney, two patients mistakenly diagnosed with renal cell cancer and underwent radical nephrectomy, two patients mistakenly diagnosed with urolithiasis but were subsequently found to have TCC, and two patients with tumour invasion to psoas.
Intravesical chemotherapy: All patients underwent a 8-week induction regimen followed by a once-monthly maintenance regimen for 12 months. The induction regimen consisted of intravesical administration of mitomycin C (20 mg) or epirubicin (50 mg) dissolved in 50 ml saline, which was retained for 60 minutes and drained once a week for 8 weeks. This procedure was followed by the maintenance regimen, which used the same dose of mitomycin or epirubicin once a month for 12 months.
Assessment of toxicity
Patients were monitored weekly by radiation oncologists for symptoms of toxicity resulting from their radiation therapy. Radiation toxicity was evaluated according to the guidelines established by the Radiation Therapy Oncology Group (RTOG; version 2.0) .
Patients were advised of the need for an initial follow-up examination at the sixth week after completion of EBRT. Patients were monitored every 3 to 6 months thereafter. Follow-up information was obtained primarily through telephone interview and follow-up was stopped on March 15, 2009. The overall survival time was defined as the interval between the date of surgery and either the date of death or the date of the last follow-up (censored).
The primary endpoint measures of the study were safety, loco-regional failure or the occurrence of distant metastasis, and overall survival. These were defined as the time from the date of nephroureterectomy. Data were censored at the date of the last visit or the date of death. The characteristics of the patients, loco-regional failure or metastasis rates, and overall survival rates were compared between patients in the RT and non-RT groups. The chi-square test was used for comparison between groups. Survival curves were calculated by the Kaplan-Meier method and compared using the log-rank test. The Cox proportional hazards model was used to determine the independent factors affecting endpoints, based on the variables selected by the univariate analysis. Statistical analyses were performed by SPSS 13.0 for Windows (SPSS Inc., Chicago, IL). P values < 0.05 were considered to be statistically significant.
Among the 133 total subjects, 53 died during follow-up, four were lost during follow-up, and the remaining 76 were censored at the end of the follow-up period on 3/15/2009. The interval between surgery and initiation of RT was 26.4 days on average with a 95% confidence interval of ± 3.14 days. The median follow-up time was 26.6 months. The age of the patients ranged from 34 to 91 years, and the mean age was 67.8 years. A similar proportion of patients with similar clinical symptoms were included in the radiation (RT) and non-radiation (non-RT) groups (Table 1).
We scheduled the full postoperative adjuvant radiation dose as 46-50 Gy, but this dosage was subject to change based on unpredicted situations that arose during the course of EBRT and indicated the need for a reduced dose, such as adverse side effects and the emergence of distant metastases. The dosage was increased to between 54 and 60 Gy for patients who underwent R1 or R2 resection (12 patients). Three patients presented with distant metastases during radiation, and four patients developed ≥ grade 2 anorexia; the radiation dose was reduced to < 46 Gy in these seven cases.
Survival analyses and prognostic factors
When we subdivided the groups based on the tumour stage of the patients, we found a significant difference between the RT and non-RT groups for patients who had a T3 or T4 tumour stage. The median survival times of these two groups were 29.9 months vs. 11.4 months (p = 0.006) for the RT and non-RT groups, respectively (Figure 2B, C).
Univariate and multivariate analysis of baseline predictors of survival in 133 patients with transitional cell carcinoma of the renal pelvis and/or ureter
Correlation with histology
< 60 years
≥ 60 years
T1 or T2
T3 or T4
R1 or R2
Grade I or II
Grade III or IV
Using multivariate analysis, we identified several favourable predictors associated with an improved overall survival, which included age < 60 years, a T1 or T2 tumour stage, absence of synchronous LN metastases, and EBRT. The histological grade factor was determined to be significantly different using univariate analysis but not significantly different based on multivariate analysis. This result is due to multicollinearity, which arises because many of the evaluated risk factors correlate with histological grade. In this study, the histological grade correlated with the tumour stage, resection models, and presence of residual disease (Table 2).
Univariate and multivariate analysis of predictors of bladder tumor relapse in 133 patients with TCC of the renal pelvis or ureter
Bladder tumor relapse
Absent (n = 95)
Present (n = 38)
< 60 years
≥ 60 years
T1 or T2
T3 or T4
R1 or R2
Grade I or II
Grade III or IV
EBRT w/o bladder
RT including bladder
Comparison of the failure patterns between the two groups*
(n = 66)
(n = 67)
Anatomic/tumor bed recurrence
Side Effects of Radiation Therapy in 67 Patients
RTOG grade (n)
Causes of death
Causes of Death in 53 Patients with TCC of the Renal Pelvis or Ureter
(n = 30)
(n = 23)
Abdominal LN metastases
Death unrelated to cancer
Although nephroureterectoumy is a curative therapy for the majority of patients who present with tumours limited to the ureteral muscularis, the rate of local-regional recurrence may be as high as 45% (57/126), as reported in a median 9-month follow-up study in patients with locally advanced disease . In addition, persistent loco-regional disease may play an important role in the subsequent development of distant metastases. Therefore, it is important to address the role of adjuvant radiation therapy, in addition to surgery, for the local and regional control of the disease, as well as to improve the overall treatment outcome. TCC of the renal pelvis and ureter is an unusual disease with insufficient clinical data; therefore, the role of EBRT in treating this disease is unclear. Czito et al.  retrospectively reviewed the records of 31 patients with locally advanced TCC of the renal pelvis and ureter who underwent surgery followed by adjuvant EBRT with or without concurrent chemotherapy [methotrexate, cisplatin and vinblastine (MCV)]. The 5-year overall and disease-free survival rates were improved in patients with locally advanced upper tract urothelial malignancies who underwent resection surgery and adjuvant concurrent chemoradiotherapy. This regimen should be considered in patients with T3/4 and/or node positive upper tract TCC. Patients with advanced disease treated with surgery alone had a shorter disease-free survival (23.3 months) than those treated with combination chemoradiotherapy (45.2 months). In our study, we also found that radiotherapy significantly reduced the rate of tumour recurrence, irrespective of the pT stage or the presence of synchronous LN. However, EBRT seemed to confer an overall survival advantage only to patients with T3/T4 stage or synchronous LN.
In this study, univariate analysis indicated that an increased overall survival was significantly associated with age < 60 years, a T1 or T2 tumour stage, no synchronous LN metastases, nephroureterectomy, R0 resection and a lower histological grade. These prognostic factors are similar to those reported by Ozsahin et al. , Tan et al. , and Raman et al. . Recently, Raman et al. reported a retrospective review of data collected from 10 global institutions, which included 1,249 patients with TCC of the renal pelvis and ureter. This study determined that advanced T stage, higher histological grade, and lymph node metastases were associated with a poorer survival outcome .
Both our univariate and multivariate analyses suggested that radiation was an effective and tolerable treatment for patients with T3 or T4 pelvis or ureteral TCC. However, there are three fundamental questions that must be answered in order to develop a comprehensive plan for performing radiotherapy in these patients:
1) What is the appropriate volume of tissue that we must irradiate to achieve the desired curative or palliative goal? The volume of tissue exposed to radiation in order to encompass the gross nodal metastases and the residual tumour, and whether to include adjacent areas of potential microscopic disease, have been controversial issues. In this study, the clinical target volume included the renal fossa, the course of the ureter to the bladder, and the paracaval and para-aortic lymph nodes, which were at risk of harbouring metastatic disease. For T1 or T2-stage patients, radiotherapy did not improve overall survival, but did delay bladder tumour relapse.
Bladder tumour recurrence following nephroureterectomy for TCC of the upper urinary tract was observed in 30-40% of patients [2, 3]. Most bladder tumour recurrences develop within 2 years following surgical resection. Cozad et al. reported that radiotherapy could significantly reduce local recurrence. There was a borderline significant increase in the overall survival (p = 0.07) for 77 patients who all had T stage renal pelvis and ureteral cancer . Multivariate analysis determined that the ureteric tumour location was an independent predictor (p = 0.02) for bladder tumour relapse, with rates of 20% (25/123) for patients with renal pelvis cancer and 40% (19/47) for patients with ureteral cancer. Our results showed that the bladder tumour relapse rates were 14.3% (6/42) for renal pelvis cancer and 35.2% (32/91) for ureteric cancer (chi-square test, p = 0.013). Based on these observations, we suggest that the clinical target volume should only include the bladder for elective radiotherapy in the case of T1 or T2 patients, especially in patients with ureteric cancer, as this regimen will effectively delay bladder tumour relapse.
2) What is the planned treatment dose? Selection of the radiation dose is a complex issue for abdominal cancer, because it requires the radiation oncologist to weigh the use of a sufficiently high radiation dose against an unacceptably high risk of side effects. Radiation complications consistently increase as the radiation dose increases. In general, the post-operation adjuvant radiation dose should be between 45 and 50 Gy, as this was established to be a safe dosage for the small bowel and colon. Usually, the length of the field from cephalic to caudal is >30 cm; however, no grade toxicity was observed in this study. Chauffert et al. reported no gastrointestinal bleeding in 119 patients with advanced pancreatic cancer who received 60 Gy radiation with conventional fractions . Therefore, a radiation dose between 45 and 50 Gy was acceptable to use in this study.
3) What are the chemotherapeutic regimens? Adjuvant chemotherapy with paclitaxel and carboplatin  or M-VAC  is feasible, may reduce the risk of distant metastases, and may prevent the recurrence of bladder tumour in patients with high-risk upper urinary tract carcinoma. There are a few controlled clinical trials using adjuvant or radical radiotherapy with or without chemotherapy in patients with renal pelvic and ureteric cancer; therefore, whether radiotherapy improves the treatment outcome is inconclusive. A study by Czito et al. reported that cisplatin-based chemotherapy concurrently delivered with radiation significantly improved the treatment outcome. Chemotherapy may further improve the treatment outcome if it is concurrently delivered with high-dose radiation. Unfortunately, we did not adopt adjuvant chemotherapy in this study, partly due to the lack of evidence supporting adjuvant chemotherapy at the time of our protocol design. However, all patients in this study received postoperative instillation of MMC or epidorubicin as a regional chemotherapy, and this regimen successfully reduced the recurrence of bladder tumours after surgery for upper urinary tract tumours . Currently, there is not enough evidence to support replacement of systemic chemotherapy with intravesical chemotherapy.
Limitations of our study included the non-randomised design and the use of several different radiation techniques, which may have been affected by selection bias, and the fact that no systemic chemotherapy regimens were included. Although our sample size was relatively large, these issues should be addressed, preferably in a prospective study using a randomised design. However, due to the rarity of this malignancy, development of the optimal treatment strategy for patients with TCC of the renal pelvis and ureter may be impossible without collaborative efforts among multiple cancer treatment institutions.
The use of adjuvant EBRT was efficacious in the treatment of TCC of the renal pelvis or ureter, as it reduced the local recurrence for all patients and improved the overall survival for those patients with T3/T4 classification. Bladder tumour recurrence was the main cause of local recurrence, so the clinical target volume should include the whole bladder for all tumour stages. Radiotherapy and chemotherapy used in an adjuvant setting is a strategy that warrants optimization and evaluation in a prospective, randomised clinical trial setting to determine whether it can further improve treatment outcome.
Impact of tumor location on prognosis for patients with upper tract urothelial carcinoma managed by radical nephroureterectomy.
- Genega EM, Porter CR: Urothelial neoplasms of the kidney and ureter. An epidemiology, pathologic and clinical review. Am J Clin Pathol. 2002, 117 (s1): s36-48.PubMedGoogle Scholar
- Zigeuner RE, Hutterer G, Chromecki T, Rehak P, Langner C: Bladder tumour development after urothelial carcinoma of the upper urinary tract is related to primary tumour location. BJU International. 2006, 98: 1181-86,. 10.1111/j.1464-410X.2006.06519.x.View ArticlePubMedGoogle Scholar
- Tan LB, Chang LL, Cheng KI, Huang CH, Kwan AL: Transitional cell carcinomas of the renal pelvis and the ureter: comparative demographic characteristics, pathological grade and stage and 5-year survival in a Taiwanese population. BJU International. 2008, 103: 312-16.View ArticlePubMedGoogle Scholar
- Kirkali Z, Tuzel E: Transitional cell carcinoma of the ureter and renal pelvis. Critical Reviews in Oncol/Hematology. 2003, 47: 155-69. 10.1016/S1040-8428(03)00079-9.View ArticleGoogle Scholar
- Raman JD, Scherr DS: Management of patients with upper urinary tract transitional cell carcinoma. Nature Clinical Practice Urology. 2007, 4: 432-443.View ArticlePubMedGoogle Scholar
- Ozsahin M, Zouhair A, Villà S, et al: Prognostic factors in urothelial renal pelvis and ureter tumours: a multicentre Rare Cancer Network study. Eur J Cancer. 1999, 35: 738-43. 10.1016/S0959-8049(99)00012-X.View ArticlePubMedGoogle Scholar
- Maulard-Durdux C, Dufour B, Hennequin C, et al: Postoperative radiation therapy in 26 patients with invasive transitional cell carcinoma of the upper urinary tract: no impact on survival?. J Urol. 1996, 155: 115-7.View ArticlePubMedGoogle Scholar
- Grigsby PW: Carcinoma of the urethra in women. Int J Radiat Oncol Biol Phys. 1998, 41: 535-541. 10.1016/S0360-3016(97)00773-6.View ArticlePubMedGoogle Scholar
- Czito B, Zietman A, Kaufman D, et al: Adjuvant radiotherapy with and without concurrent chemotherapy for locally advanced transitional cell carcinoma of the renal pelvis and ureter. J Urol. 2004, 172 (4 Pt 1): 1271-1275.View ArticlePubMedGoogle Scholar
- American Joint Committee on Cancer: Renal pelvis and ureter. AJCC cancer staging manual. Edited by: Greene FL, et al. 2002, New York: Springer-Verlag, 329-334. 6View ArticleGoogle Scholar
- Trotti A, Byhardt R, Stetz J, et al: Common Toxicity Criteria (version 2.0): An improved reference for grading the acute effects of cancer treatment--Impact on radiotherapy. Int J Radiat Oncol Biol Phys. 2000, 47: 13-47. 10.1016/S0360-3016(99)00559-3.View ArticlePubMedGoogle Scholar
- Raman JD, Ng CK, Scherr DS, et al: Impact of tumor location on prognosis for patients with upper tract urothelial carcinoma managed by radical nephroureterectomy. European Urol. 2009, 57: 1072-9.View ArticleGoogle Scholar
- Cozad SC, Smalley SR, Austenfeld M, Noble M, Jennings S, Raymond R: Transitional cell carcinoma of the renal pelvis or ureter: patterns of failure. Urology. 1995, 46: 796-800. 10.1016/S0090-4295(99)80346-X.View ArticlePubMedGoogle Scholar
- Chauffert B, Mornex F, Bonnetain F, et al: Phase III trial comparing intensive induction chemoradiotherapy (60 Gy, infusional 5-FU and intermittent cisplatin) followed by maintenance gemcitabine with gemcitabine alone for locally advanced unresectable pancreatic cancer. Definitive results of the 2000-01 FFCD/SFRO study. Ann Oncol. 2008, 19: 1592-9. 10.1093/annonc/mdn281.View ArticlePubMedGoogle Scholar
- Bamias A, Deliveliotis Ch, Fountzilas G, et al: Adjuvant chemotherapy with paclitaxel and carboplatin in patients with advanced carcinoma of the upper urinary tract: a study by the Hellenic cooperative oncology group. J Clin Oncol. 2004, 22: 2150-54. 10.1200/JCO.2004.09.043.View ArticlePubMedGoogle Scholar
- Soga N, Arima K, Sugimura Y: Adjuvant methotrexate, vinblastine, adriamycin, and cisplatin chemotherapy has potential to prevent recurrence of bladder tumors after surgical removal of upper urinary tract transitional cell carcinoma. Int J Urol. 2008, 15: 800-803. 10.1111/j.1442-2042.2008.02114.x.View ArticlePubMedGoogle Scholar
- Sakamoto N, Naito S, Kumazawa J, et al: Prophylactic intravesical instillation of mitomycin C and cytosine arabinoside for prevention of recurrent bladder tumors following surgery for upper urinary tract tumors: a prospective randomized study. Int J Urology. 2001, 8: 212-16. 10.1046/j.1442-2042.2001.00286.x.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/11/297/prepub
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