Next Article in Journal
Metabolism and Intracranial Epileptogenicity in Temporal Lobe Long-Term Epilepsy-Associated Tumor
Next Article in Special Issue
Prognostic Utility of the Modified Glasgow Prognostic Score in Urothelial Carcinoma: Outcomes from a Pooled Analysis
Previous Article in Journal
Impact of COVID-19 Pandemic on Initiation of Immunosuppressive Treatment in Immune-Mediated Inflammatory Diseases in Austria: A Nationwide Retrospective Study
Previous Article in Special Issue
A Systematic Review on the Role of Repeat Transurethral Resection after Initial en Bloc Resection for Non-Muscle Invasive Bladder Cancer
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Prognostic Significance of Organ-Specific Metastases in Patients with Metastatic Upper Tract Urothelial Carcinoma

1
Department of Urology, University Sapienza, 00185 Rome, Italy
2
Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, Department of Biology, College of Science and Technology, Temple University, Philadelphia, PA 19122, USA
3
Department of Biomedical Sciences, Humanitas University, 20072 Pieve Emanuele, Italy
4
Department of Precision Medicine, University of Campania “L. Vanvitelli”, 80138 Naples, Italy
5
Urology Unit, AORN Ospedali dei Colli-Monaldi Hospital, 80131 Naples, Italy
6
Department of Urology, Regina Elena National Cancer Institute, 00144 Rome, Italy
7
Department of Medical Biotechnology, University of Siena, 53100 Siena, Italy
*
Authors to whom correspondence should be addressed.
J. Clin. Med. 2022, 11(18), 5310; https://doi.org/10.3390/jcm11185310
Submission received: 23 August 2022 / Accepted: 2 September 2022 / Published: 9 September 2022
(This article belongs to the Special Issue Urothelial Carcinoma: Clinical Diagnosis and Treatment)

Abstract

:
Background: Existing data on metastatic upper tract urothelial carcinoma (mUTUC) are limited. In this study, we investigated the prognostic value of site-specific metastases in patients with mUTUC and its association with survival outcomes. Methods: We retrospectively collected data from the Surveillance, Epidemiology and End Results (SEER) database between 2004 and 2016. Kaplan–Meier analysis with a log-rank test was used for survival comparisons. Multivariate Cox regression was employed to predict overall survival (OS) and cancer-specific survival (CSS). Results: 633 patients were selected in this study cohort. The median follow-up was 6 months (IQR 2–13) and a total of 584 (92.3%) deaths were recorded. Within the population presenting with a single metastatic organ site, the most common metastatic sites were distant lymph nodes, accounting for 36%, followed by lung, bone and liver metastases, accounting for 26%, 22.8% and 16.2%, respectively. In patients with a single metastatic organ site, the Kaplan–Meier curves showed significantly worse OS for patients with liver metastases vs. patients presenting with metastases in a distant lymph node (p < 0.001), bone (p = 0.023) or lung (p = 0.026). When analyzing CSS, statistically significant differences were detectable only between patients presenting with liver metastases vs. distant lymph node metastases (p < 0.001). Multivariate analyses showed that the presence of liver (OS: HR = 1.732, 95% CI = 1.234–2.430, p < 0.001; CSS: HR = 1.531, 95% CI = 1.062–2.207, p = 0.022) or multiple metastatic organ sites (OS: HR = 1.425, 95% CI = 1.159–1.753, p < 0.001; CSS: HR = 1.417, 95% CI = 1.141–1.760, p = 0.002) was an independent predictor of poor survival. Additionally, survival benefits were found in patients undergoing radical nephroureterectomy (RNU) (OS: HR = 0.675, 95% CI = 0.514–0.886, p = 0.005; CSS: HR = 0.671, 95% CI = 0.505–0.891, p = 0.006) and chemotherapy (CHT) (OS: HR = 0.405, 95% CI = 0.313–0.523, p < 0.001; CSS: HR = 0.435, 95% CI = 0.333–0.570, p < 0.001). Conclusions: A distant lymph node was the most common site of single-organ metastases for mUTUC. Patients with liver metastases and patients with multiple organ metastases exhibited worse survival outcomes. Lastly, CHT administration and RNU were revealed to be predictors of better survival outcomes in the mUTUC cohort.

1. Introduction

Upper tract urothelial carcinoma (UTUC) is a rare malignancy that accounts for 5% to 10% of all urothelial cancers. The annual incidence of UTUC is typically estimated at 2 per 100,000 people in Western countries, with a peak in individuals aged from 70 to 90 years [1].
In patients with a diagnosis of UTUC, the 3-year overall survival (OS) rate is around 75% [2]. However, when considering metastatic UTUC (mUTUC) patients, the 3-year OS rate does not exceed 10% [3].
Recently, the prognostic role of metastasis at distant organs was investigated in multiple types of cancers [4,5,6]. To date, data on metastatic urothelium carcinoma are mainly based on studies on urothelial bladder cancer (UBC). For example, Shou et al. reported that the presence of liver metastasis was an independent predictor of OS when compared with other metastatic organ sites in metastatic bladder cancer (mBCa) [7]. Moreover, Dong et al. suggested that patients with mBCa exhibiting more than one metastatic site presented with unfavorable survival outcomes. Based on these results, we hypothesized that organ-specific metastases might also play a role in the prognosis of mUTUC [8].
Hence, our purpose was to retrospectively investigate the impact of organ-specific mUTUC patients on prognostic survival outcomes.

2. Materials and Methods

2.1. Database and Patient Selection

In January 2022, we interrogated the Surveillance, Epidemiology and End Results (SEER) database and identified patients with mUTUC from 2004 to 2016 according to the following inclusion criteria: (1) aged ≥ 18 years; (2) UTUC with distant metastasis as the first primary malignancy; (3) pathologically confirmed mUTUC of the renal pelvis, ureter or ureter orifice (International Classification of Disease for Oncology (ICD-O) site codes C65.9, C66.9 and C67.6, respectively); and (4) enrolled patients should have confirmed information on metastases in their bone, liver, lung, brain or distant lymph node. We excluded any metastatic pattern presented in less than 20 patients. The inclusion process is presented in Supplementary Figure S1. SEER*Stat software (SEER*Stat 8.2.3) was used to extract data.

2.2. Study Outcomes

Overall survival (OS) and cancer-specific survival (CSS) were the two major outcomes of this study. OS was defined as the interval of time from the UTUC diagnosis to death for any cause. CSS was defined as the interval from the date of UTUC diagnosis to death due to the tumor.

2.3. Statistical Analysis

Demographic factors were reported as frequency and proportion. The Mantel–Cox log-rank test was applied to compare the Kaplan–Meier survival curves for OS and CSS. Univariable and multivariable Cox proportional models with hazard ratios (HRs) and 95% confidence intervals (95% CIs) addressing both OS and CSS were performed. Two-sided p-values < 0.05 were considered significant. Statistical analysis was carried out using the Statistical Package for Social Sciences (SPSS) software v.26.0 (IBM Corp, Armonk, NY, USA).

3. Results

3.1. Demographic and Clinical Characteristics

The demographic characteristics of the included patients are shown in Table 1. A total of 633 mUTUC patients were identified after applying the inclusion/exclusion criteria. The median age at diagnosis was 72 years (IQR 63–79). mUTUC patients were more frequently males (57.8%) and ethnically white (83.6%). According to the AJCC Sixth edition TNM stage, 322 (50.9%) of the patients harbored a T-stage ≥ 2 and 431 (68.1%) had a positive N-stage. Furthermore, 354 (55.9%) mUTUC patients received chemotherapy (CHT) and 247 (39%) underwent radical nephroureterectomy (RNU). The median follow-up period was 6 months (IQR 2–13) and a total of 584 (92.3%) deaths were recorded.

3.2. Metastatic Patterns

Information on the metastatic organs is summarized in Table 1. Overall, 65.9% (n = 417) of the included population presented with a single metastatic organ site. Of those, the distribution showed that 36% (n = 147) were diagnosed with distant lymph nodes metastases, followed by lung, bone and liver metastases accounting for 26.0% (n = 106), 21.8% (n = 89) and 16.2% (n = 66), respectively. Moreover, 34.1% (n = 216) of patients presented with two or more metastatic organ sites.

3.3. Impact of Metastatic Sites and Treatment Scheme on Survival Outcomes

First, the OS and CSS were analyzed according to single- vs. multiple-organ metastases. Our results revealed that patients with a single metastatic organ site had significantly better outcomes for both OS (p < 0.001) and CSS (p < 0.001) (Figure 1a,b).
Second, we focused on the OS and CSS in patients with a single metastatic organ site. Here, statistically significant differences were recorded between the Kaplan–Meier curves, showing worse outcomes in terms of OS for patients presenting liver metastases when compared with patients presenting distant lymph node (p < 0.001), bone (p < 0.023) and lung (p < 0.026) metastases (Figure 1a). Additionally, a difference was recorded between patients with lung vs. bone metastases (p = 0.026). When analyzing the CSS, a statistically significant difference was found only between liver vs. distant lymph node metastases (p < 0.001) (Figure 2a,b).
Third, we analyzed survival outcomes stratified by the treatment scheme (yes-CHT vs. no-CHT groups and yes-RNU vs. no-RNU groups) in patients harboring either single- or multiple metastatic organ sites.
Here, statistically significant differences were recorded, showing better survival outcomes in the yes-CHT vs. no-CHT group for both single- and multiple metastatic organ sites (OS and CSS: each p < 0.001). Additionally, in the subset of yes-CHT patients, better outcomes were recorded for single vs. multiple metastatic organ sites (OS: p = 0.003, CSS p = 0.011) (Figure 3a,b).
When focusing on RNU treatment, we observed better survival outcomes in the yes-RNU vs. no-RNU group for single (OS: p = 0.022, CSS: p = 0.010) and multiple metastatic organ sites (OS and CSS: each p < 0.001). Lastly, in the subset of yes-RNU patients, better outcomes were observed in the single- vs. multiple-site groups (OS: p = 0.197, CSS p = 0.234) (Figure 4a,b).
The parameters age, sex, T-stage, N-stage, surgery of primary site, CHT and number of organ metastases were included in the multivariable Cox regression model (Table 2). Our analysis showed that the subgroup of patients presenting liver metastases had lower OS than patients with distant lymph node metastases (HR = 1.732, 95% CI: 1.234–2.430, p < 0.001). Similar results were found for CSS (HR = 1.531, 95% CI: 1.062–2.207, p = 0.022). Moreover, when comparing the number of metastatic organ sites (single vs. multiple), significantly longer OS (HR = 1.425, 95% CI: 1.159–1.753, p = < 0.001) and CSS (HR = 1.417, 95% CI: 1.141–1.760, p = 0.002) were observed in patients with single-organ metastases. Finally, patients undergoing RNU and CHT showed benefit in terms of OS and CSS (RNU—OS: HR = 0.675, 95% CI: 0.514–0.886, p = 0.005; CSS: HR = 0.671, 95% CI: 0.505–0.891; p = 0.006) (CHT—OS: HR = 0.405, 95% CI: 0.313–0.523, p < 0.001; CSS: HR = 0.435, 95% CI: 0.333–0.570, p < 0.001).

4. Discussion

Previous studies demonstrated that advanced UTUC is aggressive and associated with a poor prognosis. At the time of diagnosis, 50–60% of patients with UTUC present locally advanced disease and up to 25% present with distant metastasis with a median OS of approximately 9 months [9,10,11]. These poor survival outcomes point out the fact that improving the treatment for this disease is still an essential issue and highlight the necessity to identify clinical factors that might improve clinical decision-making. Thus, in this study, we aimed at describing the pattern and frequency of metastatic sites and the prognostic relevance of any specific metastatic site by retrospectively analyzing a large patient cohort using the SEER database.
First, we observed important differences in metastatic sites, where we discovered a high frequency of distant lymph node metastases in patients that presented with a single metastatic organ site. These results are in disagreement with data reported from other mUTUC cohorts, as Chen et al. found that the lung represented the most common metastatic site, accounting for 42.3% of the whole cohort [12]. A possible interpretation of this difference might be that their analysis was limited to mUTUC presenting with a renal pelvis primary.
Second, our analysis focused on OS and CSS. Here, patients presenting with multiple metastases had worse OS and CSS according to Kaplan–Meier curves, which was confirmed using Cox regression analysis (OS: HR = 1.425, CSS: HR = 1.417). This finding is likely supported by the fact that the increase in tumor burden is usually associated with aggressive tumors and, at the same time, limits the possibility of a radical approach that can be used in oligometastatic patients (i.e., surgery or radiotherapy) [13]. Similar to our work, Li et al. analyzed the prognostic factors for OS in patients with mUTUC; the results of their multivariate analysis showed that the number of metastatic organs (1–2 vs. ≥3) outperformed the presence of visceral metastasis [14]. Additionally, Chen et al. reported that patients with ≤2 metastatic sites presented improved survival outcomes when compared with ≥3 metastatic sites [12].
Third, patients presenting with liver metastases had worse OS and CSS, as shown by the Kaplan–Meier curves. Our observations were also confirmed after multivariate adjustments for patient and tumor characteristics, where we identified a statistically significant OS and CSS disadvantage in patients with liver metastases relative to distant lymph node metastases (OS: HR = 1.732, CSS: HR = 1.531). Similarly, Dong et al. demonstrated that patients with liver metastases had worse OS rather than CSS, which provides a possible explanation [8]. Nonetheless, Shou et al. reported that mBCa patients with liver metastasis (SEER database; 2010–2014) exhibited worse OS compared with three other single metastatic organ sites [7]. A possible explanation for these results might be attributed to liver failure and, consequently, an increased overall mortality rate.
Fourth, our analyses focused on CHT administration. CHT is currently the accepted treatment option for advanced UTUC but the majority of data are extrapolated from UBC. In our cohort, CHT was associated with favorable OS (HR = 0.405) and CSS (HR = 0.435). Similar results were reported by Nazzani et al. in a non-surgically treated mUTUC population [15]. In our study, we confirmed the prognostic benefit of CHT in patients with either single or multiple metastatic organ sites. In contrast, Vassilakopoulou et al. demonstrated that adjuvant postoperative CHT does not add any significant benefit with regard to OS in high-risk UTUC patients [16]. However, in this cohort, patients with both locally advanced M0 and M+ were included. Unfortunately, within the SEER database, the proportion of patients that received cisplatin-based CHT vs. carboplatin-based CHT, as well as patients that received adjuvant vs. neoadjuvant CHT, is not specified. Moreover, we were unable to determine the rationale for determining patient exclusion from CHT regimens. However, we registered an administration rate of 55.9%, which is in line with the rates published by Browne et al. based on a large National Cancer Database (NCDB, 2004–2013) [17].
Sixth, we observed a statically significant association between radical nephroureterectomy (RNU) and OS (HR = 0.675) and CSS (HR = 0.671) after multivariable adjustments. Our findings are in agreement with several observational studies that addressed the role of surgery on primary tumor sites for mUTUC, especially in patients fit enough to receive cisplatin-based CHT [18,19].
Taken together, these data described the metastatic patterns of mUTUC and prognosis outcomes. Our results suggested that patients that presented with liver metastases had worse survival outcomes when compared with other metastatic sites. Moreover, patients that presented with metastasis at multiple secondary sites showed a worse prognosis, which was probably related to the greater burden of the disease. Nonetheless, CHT and RNU were found to be protective variables in the multivariate regression survival analysis.
We are aware of the limitations of our work, which should be interpreted in the context of its retrospective and population-based design. The SEER database included only five specific metastatic organs and the information reporting the number of metastases in each organ was not available. In addition, the SEER database does not ascertain either the type or delivery timing of chemotherapy. However, our analysis included a big population of mUTUC and our results can help to better understand and stratify prognoses, as well as justify more aggressive treatment strategies in oligometastatic patients.

5. Conclusions

Our analysis showed that a distant lymph node was the most common site of single-organ metastases for mUTUC. Patients with liver metastases and patients with multiple metastatic organ sites exhibited worse survival outcomes. Moreover, CHT administration and RNU were revealed to be predictors of better survival outcomes in the mUTUC cohort. These findings can be useful to stratify prognoses of mUTUC and justify aggressive treatment in oligometastatic patients.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcm11185310/s1, Figure S1: Flowchart of patients included.

Author Contributions

Conceptualization, A.T. and N.C.; methodology, A.M.; software, F.D.; validation, R.S.F. and A.M.; formal analysis, A.T. and V.N.; investigation, A.T. and N.C.; resources, A.G.; data curation, R.R. and F.B.; writing—original draft preparation, A.T. and N.C.; writing—review and editing, A.T. and A.M.; visualization, C.L.; supervision, A.G., A.M. and U.A.; project administration, A.T. and A.M.; funding acquisition, A.G. All authors have read and agreed to the published version of the manuscript.

Funding

The APC was funded by the Sbarro Health Research Organization.

Institutional Review Board Statement

Ethical review and approval were waived for this study due to the data being extracted from the SEER database.

Informed Consent Statement

Patient consent was waived due to the data being extracted from the SEER database.

Data Availability Statement

https://seer.cancer.gov, accessed on 1 July 2022.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Siegel, R.L.; Miller, K.D.; Fuchs, H.E.; Jemal, A. Cancer statistics, 2022. CA Cancer J Clin. 2022, 72, 7–33. [Google Scholar] [CrossRef] [PubMed]
  2. Wang, Q.; Zhang, T.; Wu, J.; Wen, J.; Tao, D.; Wan, T.; Zhu, W. Prognosis and risk factors of patients with upper urinary tract urothelial carcinoma and postoperative recurrence of bladder cancer in central China. BMC Urol. 2019, 19, 24. [Google Scholar] [CrossRef] [PubMed]
  3. Raman, J.D.; Messer, J.; Sielatycki, J.A.; Hollenbeak, C.S. Incidence and survival of patients with carcinoma of the ureter and renal pelvis in the USA, 1973–2005. Br. J. Urol. Int. 2011, 107, 1059–1064. [Google Scholar] [CrossRef] [PubMed]
  4. Oweira, H.; Petrausch, U.; Helbling, D.; Schmidt, J.; Mannhart, M.; Mehrabi, A.; Schöb, O.; Giryes, A.; Decker, M.; Abdel-Rahman, O. Prognostic value of site-specific metastases in pancreatic adenocarcinoma: A Surveillance Epidemiology and End Results database analysis. World J. Gastroenterol. 2017, 23, 1872–1880. [Google Scholar] [CrossRef] [PubMed]
  5. Wu, S.-G.; Li, H.; Tang, L.-Y.; Sun, J.-Y.; Zhang, W.-W.; Li, F.-Y.; Chen, Y.-X.; He, Z.-Y. The effect of distant metastases sites on survival in de novo stage-IV breast cancer: A SEER database analysis. Tumour Biol. J. Int. Soc. Oncodevelopmental. Biol. Med. 2017, 39, 1010428317705082. [Google Scholar] [CrossRef] [PubMed]
  6. Abdel-Rahman, O. Clinical correlates and prognostic value of different metastatic sites in metastatic renal cell carcinoma. Future Oncol. 2017, 13, 1967–1980. [Google Scholar] [CrossRef] [PubMed]
  7. Shou, J.; Zhang, Q.; Zhang, D. The prognostic effect of metastasis patterns on overall survival in patients with distant metastatic bladder cancer: A SEER population-based analysis. World J. Urol. 2021, 39, 4151–4158. [Google Scholar] [CrossRef] [PubMed]
  8. Dong, F.; Fu, H.; Shi, X.; Shen, Y.; Xu, T.; Gao, F.; Wang, X.; Zhong, S.; Ding, Q.; Shen, Z.; et al. How do organ-specific metastases affect prognosis and surgical treatment for patients with metastatic upper tract urothelial carcinoma: First evidence from population based data. Clin. Exp. Metastasis 2017, 34, 467–477. [Google Scholar] [CrossRef] [PubMed]
  9. Bellmunt, J.; von der Maase, H.; Mead, G.M.; Skoneczna, I.; De Santis, M.; Daugaard, G.; Boehle, A.; Chevreau, C.; Paz-Ares, L.; Laufman, L.R.; et al. Randomized phase III study comparing paclitaxel/cisplatin/gemcitabine and gemcitabine/cisplatin in patients with locally advanced or metastatic urothelial cancer without prior systemic therapy: EORTC Intergroup Study 30987. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 2012, 30, 1107–1113. [Google Scholar] [CrossRef] [PubMed]
  10. Rink, M.; Ehdaie, B.; Cha, E.K.; Green, D.A.; Karakiewicz, P.I.; Babjuk, M.; Margulis, V.; Raman, J.D.; Svatek, R.S.; Fajkovic, H.; et al. Stage-specific impact of tumor location on oncologic outcomes in patients with upper and lower tract urothelial carcinoma following radical surgery. Eur. Urol. 2012, 62, 677–684. [Google Scholar] [CrossRef] [PubMed]
  11. Margulis, V.; Shariat, S.F.; Matin, S.F.; Kamat, A.M.; Zigeuner, R.; Kikuchi, E.; Lotan, Y.; Weizer, A.; Raman, J.; Wood, C.G.; et al. Outcomes of radical nephroureterectomy: A series from the Upper Tract Urothelial Carcinoma Collaboration. Cancer 2009, 115, 1224–1233. [Google Scholar] [CrossRef] [PubMed]
  12. Chen, W.-K.; Wu, Z.-G.; Xiao, Y.-B.; Wang, Q.-Q.; Yu, D.-D.; Cai, J.; Zhou, C.-F. Prognostic Value of Site-Specific Metastases and Therapeutic Roles of Surgery and Chemotherapy for Patients with Metastatic Renal Pelvis Cancer: A SEER Based Study. Technol. Cancer Res. Treat. 2021, 20, 15330338211004914. [Google Scholar] [CrossRef] [PubMed]
  13. Palma, D.A.; Olson, R.; Harrow, S.; Gaede, S.; Louie, A.V.; Haasbeek, C.; Mulroy, L.; Lock, M.; Rodrigues, G.B.; Yaremko, B.P.; et al. Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 2020, 38, 2830–2838. [Google Scholar] [CrossRef] [PubMed]
  14. Li, X.; Li, S.; Chi, Z.; Cui, C.; Si, L.; Yan, X.; Mao, L.; Lian, B.; Tang, B.; Wang, X.; et al. Clinicopathological characteristics, prognosis, and chemosensitivity in patients with metastatic upper tract urothelial carcinoma. Urol. Oncol. 2021, 39, e1–e75. [Google Scholar] [CrossRef] [PubMed]
  15. Nazzani, S.; Preisser, F.; Mazzone, E.; Marchioni, M.; Bandini, M.; Tian, Z.; Mistretta, F.A.; Shariat, S.F.; Soulières, D.; Montanari, E.; et al. Survival Effect of Chemotherapy in Metastatic Upper Urinary Tract Urothelial Carcinoma. Clin. Genitourin. Cancer 2019, 17, e97–e103. [Google Scholar] [CrossRef] [PubMed]
  16. Vassilakopoulou, M.; Rouge, T.D.L.M.; Colin, P.; Ouzzane, A.; Khayat, D.; Dimopoulos, M.; Papadimitriou, C.A.; Bamias, A.; Pignot, G.; Nouhaud, F.X.; et al. Outcomes after adjuvant chemotherapy in the treatment of high-risk urothelial carcinoma of the upper urinary tract (UUT-UC): Results from a large multicenter collaborative study. Cancer 2011, 117, 5500–5508. [Google Scholar] [CrossRef] [PubMed]
  17. Browne, B.M.; Stensland, K.D.; Moynihan, M.J.; Canes, D. An Analysis of Staging and Treatment Trends for Upper Tract Urothelial Carcinoma in the National Cancer Database. Clin. Genitourin. Cancer 2018, 16, e743–e750. [Google Scholar] [CrossRef] [PubMed]
  18. Seisen, T.; Jindal, T.; Karabon, P.; Sood, A.; Bellmunt, J.; Rouprêt, M.; Leow, J.J.; Vetterlein, M.; Sun, M.; Alanee, S.; et al. Efficacy of Systemic Chemotherapy Plus Radical Nephroureterectomy for Metastatic Upper Tract Urothelial Carcinoma. Eur. Urol. 2017, 71, 714–718. [Google Scholar] [CrossRef] [PubMed]
  19. Moschini, M.; Xylinas, E.; Zamboni, S.; Mattei, A.; Niegisch, G.; Yu, E.Y.; Bamias, A.; Agarwal, N.; Sridhar, S.S.; Sternberg, C.N.; et al. Efficacy of Surgery in the Primary Tumor Site for Metastatic Urothelial Cancer: Analysis of an International, Multicenter, Multidisciplinary Database. Eur. Urol. Oncol. 2020, 3, 94–101. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Kaplan–Meier plots depicting the OS (a) and CSS (b) according to single vs. multiple metastatic organ(s) patients.
Figure 1. Kaplan–Meier plots depicting the OS (a) and CSS (b) according to single vs. multiple metastatic organ(s) patients.
Jcm 11 05310 g001
Figure 2. Kaplan–Meier plots depicting OS (a) and CSS (b) according to different metastatic organs in patients presenting single-organ metastases. DL, distant lymph node.
Figure 2. Kaplan–Meier plots depicting OS (a) and CSS (b) according to different metastatic organs in patients presenting single-organ metastases. DL, distant lymph node.
Jcm 11 05310 g002
Figure 3. Kaplan–Meier plots depicting OS (a) and CSS (b) according to chemotherapy (CHT) administration in patients with single- vs. multiple-organ metastases.
Figure 3. Kaplan–Meier plots depicting OS (a) and CSS (b) according to chemotherapy (CHT) administration in patients with single- vs. multiple-organ metastases.
Jcm 11 05310 g003
Figure 4. Kaplan–Meier plots depicting OS (a) and CSS (b) according to radical nephroureterectomy (RNU) treatment in patients with single- vs. multiple-organ metastases.
Figure 4. Kaplan–Meier plots depicting OS (a) and CSS (b) according to radical nephroureterectomy (RNU) treatment in patients with single- vs. multiple-organ metastases.
Jcm 11 05310 g004
Table 1. Baseline characteristics of patients with metastatic UTUC.
Table 1. Baseline characteristics of patients with metastatic UTUC.
CharacteristicsNo.%
Age (years)
<6517627.8
≥6545772.2
Gender
Female26742
Male36657.8
(T)NM
X15123.8
0–216025.3
3–432250.9
T(N)M
020231.9
>143168.1
Grade
Low15925.1
High47474.9
Race
White52983.6
Black386.0
Other6610.4
Radiation
No548.5
Yes12219.3
Unknown45772.2
Radical nephroureterectomy
No38661.0
Yes24739.0
Chemotherapy
No19530.8
Yes35455.9
Unknown8413.3
Primary site
Renal pelvis42767.5
Ureter16626.2
Ureteric orifice406.3
Number of metastatic sites
Single organ site41765.9
Multiple organ sites21634.1
Table 2. Multivariate Cox regression analysis of factors that influenced OS and CSS outcomes.
Table 2. Multivariate Cox regression analysis of factors that influenced OS and CSS outcomes.
FactorsMedian OS (Months) HR (95% CI)p-ValueMedian CSS (Months)
HR (95% CI)
p-Value
Age (years)
<65Reference
≥651.196 (0.903–1.584)0.2131.167 (0.871–1.564)0.301
Gender
FemaleReference
Male0.900 (0.705–1.148)0.3940.946 (0.732–1.221)0.946
Tumor location
Renal pelvisReference
Ureter0.782 (0.592–1.034)0.0850.715 (0.530–0.965)0.028
Ureter orifice1.044 (0.656–1.662)0.8551.023 (0.630–1.662)0.926
(T)NM
1–2Reference
3–41.16 (0.869–1.553)0.3120.946 (0.732–1.221)0.668
T(N)M
0Reference
≥10.962 (0.733–1.262)0.7771.003 (0.753–1.337)0.983
Number of organ metastasis
Single organ siteReference
Multiple organ sites1.425 (1.159–1.753)<0.0011.417 (1.141–1.760)0.002
Radical nephroureterectomy
NoReference
Yes0.675 (0.514–0.886)0.0050.671 (0.505–0.891)0.006
Distant metastasis
Lymph nodeReference
Liver1.732 (1.234–2.430)0.0011.531 (1.062–2.207)0.022
Bone1.188 (0.849–1.663)0.3151.219 (0.863–1.721)0.261
Lung1.179 (0.861–1.615)0.3041.138 (0.817–1.585)0.444
Chemotherapy
NoReference
Yes0.405 (0.313–0.523)<0.0010.435 (0.333–0.570)<0.001
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Tufano, A.; Cordua, N.; Nardone, V.; Ranavolo, R.; Flammia, R.S.; D’Antonio, F.; Borea, F.; Anceschi, U.; Leonardo, C.; Morrione, A.; et al. Prognostic Significance of Organ-Specific Metastases in Patients with Metastatic Upper Tract Urothelial Carcinoma. J. Clin. Med. 2022, 11, 5310. https://doi.org/10.3390/jcm11185310

AMA Style

Tufano A, Cordua N, Nardone V, Ranavolo R, Flammia RS, D’Antonio F, Borea F, Anceschi U, Leonardo C, Morrione A, et al. Prognostic Significance of Organ-Specific Metastases in Patients with Metastatic Upper Tract Urothelial Carcinoma. Journal of Clinical Medicine. 2022; 11(18):5310. https://doi.org/10.3390/jcm11185310

Chicago/Turabian Style

Tufano, Antonio, Nadia Cordua, Valerio Nardone, Raffaele Ranavolo, Rocco Simone Flammia, Federica D’Antonio, Federica Borea, Umberto Anceschi, Costantino Leonardo, Andrea Morrione, and et al. 2022. "Prognostic Significance of Organ-Specific Metastases in Patients with Metastatic Upper Tract Urothelial Carcinoma" Journal of Clinical Medicine 11, no. 18: 5310. https://doi.org/10.3390/jcm11185310

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop