Abstract

Results

We identified 121 potentially relevant abstracts in our initial search. Of these, 86 were unrelated or not original research articles. Upon closer examination, 16 studies were excluded for the following reasons: one study was review; 11 studies did not provide sufficient information to estimate a summary HR and its 95% CI; three studies concerned about the effect of types of surgery; and one study just analysed different tumor location on the ureter, leaving 17 studies for reviewing^{11,14,15,17,18,19,20,21,22,23,24,25,26,27,28,29,30}.

Ureteral versus renal pelvic tumors

The univariable- and multivariable-adjusted HRs for each study and combination of all studies for the effect of ureteral and renal pelvic tumors on RFS were shown in Figure 1. In univariable analysis, the pooled estimates revealed that tumor location(p = 0.081) were not associated with recurrence. However, after adjusted for all covariates, tumor location(p < 0.001) revealed obviously associated with disease recurrence in multivariable analysis (Table 2). The combined results indicated that ureteral urothelial carcinoma was significantly with a higher tumor recurrence than renal pelvic urothelial carcinoma. A statistically significant heterogeneity was detected among studies of effects on RFS stratifying according to tumor location in multivariable analysis. We also performed sensitivity analysis by sequentially excluding one study in each turn to examine the influence of a single study on the overall estimate or in any strata. The results showed that none of the study could considerably affect the summary of risk estimates in our meta-analysis (data not shown). It confirmed the stability of our results.

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Figure 1

Meta-analysis of the effect of tumor location on RFS in univariable analysis and in multivariable analysis.

The lower and upper confidence interval (CI) values refer to 95% CIs. RFS recurrence-free survival.

For the impact of tumor location on CSS of patients with UTUC, no significant differences were found in CSS between ureteral and renal pelvic tumors(p = 0.118) in univariable analysis. However, the combined results of multivariable analysis revealed that tumor location(p < 0.001) was independently associated with CSS. The pooled HR was 1.456 for ureteral tumors versus renal pelvic tumors (Figure 2), the tumors originated from the ureter were associated with worse CSS (Table 2). From the results of sensitivity analysis, we concluded the source of heterogeneity among all the included studies probably also came from Isbarn and colleagues¹⁹.

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Figure 2

Meta-analysis of the effect of tumor location on CSS in univariable analysis and in multivariable analysis.

The lower and upper confidence interval (CI) values refer to 95% CIs. CSS cancer-specific survival.

Multifocal versus unifocal tumors

When we stratified the analysis according to multifocal and unifocal upper tract urothelial carcinoma, the pooled HR of FRS(Figure 3) indicated that multifocality was with a higher frequency of tumor recurrence than unifocal tumors either in univariable analysis(p < 0.001) or in multivariable analysis(p = 0.048) (Table 2). Sensitivity analysis showed that the significant heterogeneity of outcome among reported trials could be attributed mainly to the trial reported by Chromecki and colleagues²³.

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Figure 3

Meta-analysis of the effect of multifocal tumors on RFS in univariable analysis and in multivariable analysis.

The lower and upper confidence interval (CI) values refer to 95% CIs. RFS recurrence-free survival.

As Figure 4 showed us, the multifocal tumors were associated with increased risk of cancer-specific death. Although the univariable analysis revealed that multifocal tumors were not statistically associated with CSS(p = 0.065), after adjustment for all covariates the combined HR indicated that multifocality was an independent predictor of CSS(p = 0.009). Sensitivity analysis identified the study reported by Chromecki and colleagues²³ as the main source of heterogeneity for CSS in multifocal tumors versus unifocal tumors.

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Figure 4

Meta-analysis of the effect of multifocal tumors on CSS in univariable analysis and in multivariable analysis.

The lower and upper confidence interval (CI) values refer to 95% CIs. CSS cancer-specific survival.

Discussion

The impact of tumor location (ureter compared with renal pelvis) on the prognosis of patients with UTUC has been a matter of debate for a long time. Because of lacking of prospective studies, a definitive conclusion regarding the impact of tumor location on UTUC prognosis can not be permitted. In this systematic review we reported evidence from 17 currently retrospective studies about the effect of tumor location on the progression and survival of UTUC tested in a total of 12094 patients. The results of this meta-analysis demonstrated the independent predictor status of tumor location on RFS and CSS, with ureteral tumors showing a worse prognosis than renal pelvic tumors after adjustment for several pathologic variables¹⁵. In addition, tumor multifocality was also approved to be an independent predictor of progression and survival in patients with UTUC.

Several interesting differences in pathologic characteristics were noted depending on tumor location. We estimated the local advanced tumors and nodal positive tumors in patients stratified by tumor location respectively. Somewhat surprisingly, renal pelvic tumors presented at a more advanced tumor stage than ureteral disease when considering pT3/4 and pN+ cancers in several studies^{11,14,18,19,22,25,26,27,28,29}. One explanation for this discrepancy could be that ureteral tumors become symptomatic earlier because of obstruction at lower stages and grades and hence become detectable by endoscopy earlier compared with renal pelvic tumors that may progress before any symptomatic manifestation of disease or obstruction². However, the pooled results of this meta-analysis failed to confirm the interesting findings. The combined RRs showed no statistical differences were detected. In some ways, it could be due to lack of regional lymphadenectomy in most cases. Regional lymphadenectomy was generally performed in patients with enlarged lymph nodes on preoperative axial imaging or with adenopathy detected during intraoperative examination. As such, most of patients in this cohort did not undergo a lymphadenectomy (pNx).

The literature evaluating the impact of tumor location on UTUC outcomes was conflicting. Our researches approved that ureteral tumors were with a worse prognosis compared with renal pelvic tumors. One postulated hypothesis to explain the worse outcome with ureteral tumors is that the presence of a thinner layer of adventitia containing an extensive plexus of blood vessels and lymphatics surrounding the ureter facilitates tumor lymphatic and haematogenous spread. Furthermore, the smooth muscle layer of the ureter is thinner, allowing for higher stage when minimal tumor invasion occurs. Comparatively, the renal pelvis displays a thicker adventitial layer with associated abundant renal parenchyma and perihilar adipose tissue that allows for wider surgical resection margins, which may provide a protective role²⁸.

Bladder tumors were the most common urothelial cancers. Previous studies showed that 15–50% of patients operated for UTUC had cancer development in the bladder during the follow-up^5,9,31,32,33. Zigeuner et al analysed 191 consecutive patients with no history of bladder cancer and operated for UTUC. Bladder tumor development was noted in 39 of 123 (32%), including 18 of 76 (24%) with renal pelvic, 16 of 34 (47%) with ureter and five of 13 with multifocal tumors (P = 0.02 for renal pelvic vs ureter). Zigeuner's research showed that patients with ureteral tumors were more likely to develop subsequent Bladder cancers³⁴. van der Poel HG et al investigated the prognostic information of anatomical location of ureter in patients with UTUC. Distally located tumors had a significantly better survival than proximally located cancers (median survival 53 months versus 16 months for tumors in the proximal ureter). In a multivariable analysis both tumor stage and location in the upper tract were predictive of disease specific survival after UTUC diagnosis¹⁶.

Multifocal tumors are defined as those tumors with two or more distinct locations within the urinary tract. Keeley et al first reported multifocality as a prognostic factor with a negative impact on RFS³⁵. Subsequent studies by Novara et al and Brown et al confirmed the prognostic role of tumor multifocality in UTUC patients^17,36. Specifically, individuals with a multifocal UTUC showed a threefold higher risk of cancer-specific mortality relative to patients without tumor multifocality. Similar to our research, we found that tumor multifocality was associated with increased risks of disease progression and cancer-specific mortality, and was an independent predictor of both RFS and CSS. Tumor multifocality is a feature of biologically aggressive disease in patients with UTUC. Potential reasons underlying the worse outcomes in patients with tumor multifocality could result from a more aggressive biologic potential of tumors in patients with tumor multifocality or a delay in diagnosis or treatment resulting in more advanced disease. Taken together, it seems that tumor multifocality could help refine clinical decision-making regarding therapy and follow-up of UTUC²³, therefore it should be routinely determined and reported by pathologists.

The heterogeneity of some variables in this study is worthy of comment. Four of ten variables exhibited significant heterogeneity (I² more than 70%). Explanations may include the following. First and foremost are the limitations inherent to the biases associated with the retrospective studies included, because of no prospective studies were identified. Second, the studies in our review were done in 3 regions, including Asia, Europe and North America, and some are international multi-institutional studies. The differences in outcomes observed might reflect genetic, environmental or cultural differences among populations. Third, some other risk factors were involved in this meta-analysis which may bring bias. For instance, the surgical approaches were different. Most RNUs were open surgeries, but some were done by laparoscopic approaches. Thus, the performance bias generated. Some studies included patients who had receipt adjuvant chemotherapy, but some studies didn't; similarly some patients with previous or synchronous bladder tumor were included but excluded by other studies. Besides, the definition of RFS was not all the same within the included studies. Most studies defined RFS as local failure in the tumor bed, regional lymph nodes, or distant metastasis^{11,14,15,18,23,28,30}. But some studies considered pathologically proven failure in the bladder as disease recurrence^22,25,26,27, which made some additional patients included. The different inclusion–exclusion criteria and sample sizes brought selection bias. A final source of heterogeneity is that the incorrect classification of multifocality. The multifocal tumor is defined as a tumor with two distinct locations within the upper urinary tract (ie, involving both the renal pelvis and ureter)²⁶. Nevertheless, some studies classified the tumors involving both the renal pelvis and the ureter (multifocal) according to the dominant tumor site (based on tumor stage, grade, or size) as renal pelvic or ureteral. Therefore, some multifocal tumors were missed in some studies, and didn't include in our review, which would produce the selection bias.

With this meta-analysis of articles from the medical literature, we demonstrate that ureteral and multifocal tumors are independent predictors of disease progression and cancer-specific survival in patients with UTUC managed by RNU. Ureteral and multifocal tumors have worse prognoses than renal pelvic tumors. And we postulate that multifocal tumors should be analysed as a distinct entity to avoid misclassification. However, available data are still sparse, and in-depth analyses of the assessed associations in the context of additional longitudinal studies are highly desirable to enable more-precise estimates and a better understanding of the prognostic role of tumor location. Future research should include more high quality, rigorous randomized trials with more stringent uniformity in data reporting to draw firm conclusions.

Methods

Acknowledgments

Footnotes

References