Department of Urology, The First Affiliated Hospital of Nanchang University, Nanchang, China
# These authors contributed equally to this work.
Objective: The study aims to assess the prognostic impact of pathological T3a upstaging in clinical T1 renal cell carcinoma (RCC) on clinical outcomes.
Methods: We performed a systematic literature search of PMC, Embase, Web of Science, and Cochrane library from inception to April 2019 for studies that investigated the prognostic significance of pathological T3a upstaging in clinical T1 RCC after surgery and conducted a standard meta-analysis on survival outcomes.
Results: Overall, nine studies including 101,505 clinical T1 RCC patients were identified, in which 5,560 (5.5%) patients were upstaged to T3a after surgical treatment. Meta-analysis results showed that pT3a upstaging from clinical T1 RCC was significantly associated with poor recurrence-free survival (RFS; pooled hazard ratio [HR] 2.16, 95% confidence interval [CI] 1.70-2.75; P<0.001), overall survival (OS; pooled HR 1.36, 95% CI 1.24-1.50; P<0.001), and cancer-specific survival (CSS; pooled HR 2.11, 95% CI 1.58-2.83; P<0.001). Subgroup analyses by surgical type demonstrated that pT3a upstaging remains a significant prognostic factor for RFS and OS in RCC patients who underwent different surgical treatments.
Conclusions: Current available evidence strongly supported that postoperative pT3a upstaging has a significant negative impact on RFS, OS, and CSS in clinical T1 RCC patients. Clinical T1 RCC patients with pT3a upstaging after surgery should be closely monitored by clinician and should receive close follow-up for their poor prognosis.
Keywords: T3a, upstaging, renal cell carcinoma, survival, meta-analysis
Renal cell carcinoma (RCC), the third most common urological malignancy worldwide, accounts for approximately 3% of all reported cancers . Its incidence continues to steadily increase in most countries and regions . In the United States, approximately 65,340 new cases are diagnosed and 14,970 RCC-related deaths occur annually . The widespread use of non-invasive radiologic imaging tools including computed tomography (CT) and ultrasonography results in the overall increase in the incidental detection of RCC, especially small renal mass [4, 5].
Currently, clinical T stage is considered to be the most important factor for treatment decision-making of a renal mass and partial nephrectomy (PN) has been recommended as the first option for the surgical treatment of T1 RCC, because it preserves renal function and provides equivalent survival outcomes that are comparable to those of radical nephrectomy (RN) [6, 7]. The widespread adoption of robotic surgery further extends the indication of PN for some complex T1 cases [8, 9]. However, microscopic perirenal fat invasion, renal sinus fat infiltration, and renal vein invasion can be missed on preoperative CT [10, 11], and thus some cases appear to be clinical T1 (cT1) pre-operation but are actually pathological T3a (pT3a) post-operation owing to extension into fat or renal vein.
This interesting clinical issue (cT1 upstaged to pT3a) has attracted extensive attention and the prognosis of patients with pT3a RCC that is upstaged from a small renal mass (cT1) remains controversial. Some recent studies have focused on the prognostic significance of pT3a upstaging in cT1 RCC undergoing nephrectomy and suggested inconsistent results. Lee et al. demonstrated that patients with RCC upstaged from clinical stage T1 to pathologic stage T3a showed shorter survival outcomes than those without upstaging. Jeong et al.  found that pathological T3a upstaging of cT1 RCC was associated with a poor recurrence-free survival, compared with pT1 disease. Nayak's study  had similar conclusion and highlighted the importance of accurate clinical staging. On the contrary, Lee's study  suggested that pT3a stage disease after PN for small RCCs had similar oncological outcomes to those of pT1a stage disease. Moreover, the studies by Ramaswamy et al.  and Roberts et al.  revealed that pathologic upstaging did not result in worsened oncological outcomes after an intermediate follow-up.
In light of these conflicting findings in previous studies, we conducted a systematic review of published relevant studies and carried out a standard meta-analysis of extracted data that can be merged to evaluate of the oncological outcomes precisely in cases upstaged from cT1 to pT3a RCC after nephrectomy.
This study was performed according to the guideline of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). Because the data were collected from published literatures, ethical approval was not needed.
A computerized bibliographic search of Electronic databases (PMC, Embase, Cochrane library and Web of Science) were carried out up to April 2019 to identify published studies investigating the prognostic significance of pT3a upstaging in cT1 RCC after surgery.
Search terms using MeSH headings, keywords, and text words consist of “upstage” or “upstaging” or “upstaged” combined with “renal tumor” or “renal cancer” or “renal cell carcinoma” or “kidney cancer”. Besides, the references cited in the relevant studies were also reviewed for possible inclusions. No language limitation existed in this process. The preliminary evaluation of identified studies were performed independently by two authors (Chen and Deng).
Inclusion criteria in our meta-analysis were literatures that confirmed the upstaging (cT1 upstaged to pT3a) by postoperative pathological examination and evaluated the impact of upstaging (cT1 upstaged to pT3a) on oncologic outcomes in cT1 RCC patients. The endpoints of oncologic outcomes included recurrence-free survival (RFS), cancer-specific survival (CSS) and overall survival (OS).
Exclusion criteria were listed as follows: (1) basic research; (2) non-original articles (letters, conference abstract, editorials, comments or review articles); (3) studies not focusing on cT1 RCC; (4) studies that discussed other forms of upstaging (cT1 upstaged to pT2 or cT2 upstaged to pT3a); (5) studies that did not provide oncologic outcomes with hazard ratio (HR) and corresponding 95% confidence interval (CI) or lacked sufficient data to achieve an estimated HRs and 95% CIs by using the methods reported by Tierney et al.
When two or more published papers by the same authors were screened, the most informative article was selected to avoid incorporating duplicated data. Two authors (Chen and Deng) independently completed the review of titles, abstracts and full-text studies. Any disagreement was resolved by discussing with the senior author (Fu).
Two independent investigators (Chen and Liu) extracted data from each eligible study independently. The following data, if available, were recorded: the first author' last name, year of publication, country or region, study period, sample size (total patients and percentage of upstaging), patients age, tumor stage, treatment, median or mean follow-up time, and oncologic outcomes (RFS or OS or CSS). After that, HRs and corresponding 95% CIs associated with these oncologic outcomes were extracted to perform cumulative analyses.
Study quality was scored using the Newcastle Ottawa Scale (NOS), which was recommended by Cochrane Collaboration for the assessment of non-randomized studies . Each literature was evaluated based on the following three domains: selection, comparability and ascertainment of outcome. The total scores were added by these three domains (ranging from 0 to 9) and more scores means better methodological quality. We defined studies with scores no less than 6 were qualified to be included in the following analysis. Discrepancies between investigators were solved through consulting the senior author (Fu).
Pooled HR with its corresponding 95% CI was calculated to evaluate the upstaging (cT1 upstaged to pT3) on the survival of cT1 RCC patients, and HR greater than one indicated a worse prognosis in patients with postoperative pathological upstaging. Statistical heterogeneity was evaluated using Cochrane Q test and I2 metrics. I2>50% indicated obvious heterogeneity among studies , and a random effect model was used to pool the results. Or else, a fixed effect model was applied. Besides, sensitivity analysis was performed by sequential omission of each single study to evaluate the stability of results. The risk of publication bias was assessed by visual inspection of the funnel plots, Begg's test  and Egger's test . All above statistical analyses were performed using the STATA version 12.0 (State Corporation, College Station, TX, USA). All statistical tests were two sided, and significant difference was considered when a P value less than 0.05.
Our search strategy identified 423 potential relevant studies from initial literature searching. Using Endnote software, a total of 111 duplicated articles were excluded. After carefully screening titles and abstracts, 290 studies were excluded based on abovementioned inclusion criteria. The remaining 22 studies were selected for full text evaluation, in which 13 studies belonged to duplicated publication or failed to offer sufficient data (HRs with corresponding 95% CI). At last, nine studies (ten cohorts) stratified our eligibility criteria and were included in the following meta-analysis, in which the study by Srivastava et al. reported the HRs and 95% CIs of two different cohorts separately (cT1a upstaged to pT3a and cT1b upstaged to pT3a). The flowchart describing the process of literature searching is shown in Figure 1.
The characteristics of nine included studies (ten cohorts) were summarized in Table 1. The enrolled studies all focused on the prognostic significance of pT3a upstaging in cT1 RCC and most of them were published in recent three years. These studies involved 101,505 cT1 RCC patients, of which 5,560 (5.5%) patients were up-staged to T3a after surgical treatment (conformed by pathological methods). PN as the only treatment for cT1 RCC was reported in four included studies, while others were treated with mixed therapies (PN&RN). These RCC patients came from different countries (United State, Korea and Canda). The sample size of each study ranged from 186 to 63,005 and the percentage of pT3a upstaging ranged from 3.2% to 31%. In term of follow up time, the median or mean duration period ranged from 23 to more than 60 months. Among the eligible nine studies, seven studies [12-15, 17, 25, 26] containing 10,456 patients were performed to evaluate the impact of pT3a upstaging on the RFS of cT1 RCC patients, six studies (seven cohorts) [12, 15, 24-27] containing 98,884 patients were conducted to investigate the OS and three studies (four cohorts) [12, 24, 26] containing 33,470 patients reported the CSS, respectively. Quality scores of these studies by NOS ranged from 7 to 9, which were considered adequate for the following meta-analysis.
Characteristics of eligible studies in the meta-analysis.
|Upstage to pT3a||Age (years)||Treatment||Follow up |
|Nayak||2016||Canada||2009-2015||1448 cT1||134(9%)||Median 59.0||PN & RN||23 months||RFS||Multi||9|
|Mouracade||2017||USA||2007-2015||1042 cT1||113(10.8%)||Median 60.0||PN||35 months||RFS, OS||Uni||8|
|Lee||2016||Korea||1997-2014||1367 cT1a||43(3.2%)||Median 53.9||PN||54 months||RFS, OS||Uni||7|
|Jeong||2016||Korea||2001-2013||987 cT1||91 (9.2%)||Mean 54.9||PN & RN||48.5 months*||RFS||Uni||7|
|Lee||2018||Korea||1997-2016||3431 cT1||215(6.3%)||Median 55.0||PN & RN||39.0 months||RFS, OS, CSS||Multi||9|
|Srivastava||2018||USA (SEER)||1998-2013||23246 cT1a|
|Median 60.0||PN||40.0 months||OS, CSS||Multi||8|
|Russell||2018||USA||1995-2015||1995 cT1||95(4.8%)||Median 61.5||PN||38.2 months||RFS, CSS, OS||Uni||9|
|Ghanie||2018||USA(NCDB)||2010-2013||63005 cT1||3380(5.4%)||Mean 60.1||PN & RN||>5 years||OS||Multi||7|
|Roberts||2005||USA||1990-1999||186 cT1||57(31%)||NA||PN & RN||52.6 months*||RFS||Uni||7|
Abbreviations: RCC: renal cell carcinoma; RFS: recurrence-free survival; OS: overall survival; CSS: cancer-specifi survival; PN: partial nephrectomy; RN: radical nephrectomy; NA: not available.
Flow chart of study selection
Subgroup analysis of the studies reporting the association of pT3a upstaging and RFS/OS of cT1 RCC.
|Subgroup||Studies||Pooled HR||95% CI||P||Heterogeneity (I2)|
|PN & RN||4||2.37||1.73-3.25||P<0.001||37.4%|
|PN & RN||2||1.39||1.25-1.56||P<0.001||0.0%|
Abbreviations: RFS: recurrence-free survival; OS: overall survival; RCC: renal cell carcinoma; HR: hazard ratio; CI: confidence interval; PN: partial nephrectomy; RN: radical nephrectomy.
There were seven studies have reported the impact of pT3a upstaging on the RFS of cT1 RCC. No evident heterogeneity existed among these studies (I2=9.6%, P=0.356), thus, a fixed effect model was used to calculate the pooled HR and its 95% CI. As presented in Figure 2, the combined results showed that the pooled HR was 2.16 and the corresponding 95% CI was 1.70-2.75 (P<0.001), which revealed that pT3a upstaging was significant associated with poorer RFS in cT1 RCC patients. Furthermore, subgroup analyses were performed by patients' ethnicity, surgical type, and analysis style. The results showed that the combined HRs estimate for RFS in Caucasian and Asian were 1.98 (P<0.001) and 2.46 (P<0.001), respectively. Besides, for patients who only underwent PN, pT3a upstaging was significant associated with poor RFS (HR=1.89, 95% CI: 1.30-2.75, P=0.001), and for those undergoing PN and RN (mixed therapies), the combined HR was 2.37 (P<0.001), which indicated that different surgical types did not affect the results. Similar findings could be found in subgroup analysis by analysis style (P<0.001).
There were six studies (seven cohorts) have reported the impact of pT3a upstaging on the OS of cT1 RCC. No evident inter-study heterogeneity was observed in these studies that focused on OS (I2=8.2%, P=0.366). A fixed model was applied to pool the results and the combined HR for OS was 1.36 (95% CI, 1.24-1.50, P<0.001), indicating that pT3a upstaging was associated with worse OS in patients with cT1 RCC (Figure 3). Further subgroup analysis demonstrated that pT3a upstaging was also associated with worse OS in Caucasian and Asian patients and in patients received PN or mixed therapies.
There were three studies (four cohorts) have reported the impact of pT3a upstaging on the CSS of cT1 RCC. As shown in Figure 4, a fixed effect model was selected because there was no evident heterogeneity among the four studies (I2=0.0%, P=0.624). The pooled results showed that pT3a upstaging had a negative impact on the CSS of cT1 RCC patients who received surgical treatment (HR=2.11, 95% CI: 1.58-2.83, P<0.001).
Sensitivity analysis was conducted by sequential omission of each single study. As shown in Figure 5, the results showed that the merged HRs of RFS, OS, and CSS did not significantly changed, which confirmed the credibility of our outcomes.
Begg's test and Egger's test, as well as visual inspection of funnel plot were performed to estimate the publication bias in our meta-analysis. Figure 6 indicated that these included studies had no evident asymmetry in the funnel plots (RFS, OS, and CSS). Besides, the results by begg's test and Egger's test for the enrolled studies assessing the survival outcomes were Pbegg=0.386, Pegger=0.152 (RFS); Pbegg=0.230, Pegger=0.230 (OS); Pbegg=0.089, Pegger=0.078 (CSS), respectively. Therefore, the abovementioned evidences revealed a low probability of publication bias in the present meta-analysis.
Forest plot of studies evaluating the association between pT3a upstaging and recurrence-free survival of cT1 renal cell carcinoma
Forest plot of studies evaluating the association between pT3a upstaging and overall survival of cT1 renal cell carcinoma
Forest plot of studies evaluating the association between pT3a upstaging and cancer-specific survival of cT1 renal cell carcinoma
Sensitive analysis of included studies. A: recurrence-free survival; B: overall survival; C: cancer-specific survival
Funnel plots for the evaluation of potential publication bias. A: recurrence-free survival; B: overall survival; C: cancer-specific survival
Epidemiological data suggested that the incidence of RCC has steadily increased in recent years. The increase might be partially attributed to the widespread use of non-invasive imaging techniques, thereby resulting in the early detection of small renal tumors. Currently, The TNM staging system remains the most widely accepted system for treatment determination . However, renal sinus fat or perirenal fat invasion or renal vein thrombosis may be missed by perioperative CT [10, 11], and thus RCC may upstage from cT1 to pT3a after surgery. This interesting clinical issue has attracted extensive attention and has been widely debated. Previous reports regarding the prognostic significance of incidental pT3 upstaging in cT1 RCC remain conflicting and controversial. Thus, we systemically review the relevant published studies and conducted a standard meta-analysis to clarify the prognostic value of postoperative pT3 upstaging in patients with cT1 RCC.
In the present research, nine studies (ten cohorts) were eligible based on the inclusion criteria. HRs of cumulative survival (RFS, OS and CSS) were summarized quantitatively by standard meta-analysis techniques. The combined results demonstrated that postoperative pT3a upstaging was significantly associated with poor RFS in patients with cT1 RCC. Similar results were found in analyses on OS and CSS. Notably, in the subgroup analysis, for patients receiving PN or mixed nephrectomy (PN and RN), pT3a upstaging from cT1 still had a negative impact on the survival, thereby indicating that different surgical types did not influence the negative prognostic significance of pT3a upstaging.
Currently, PN has been the standard treatment for T1 RCC, because it preserves renal function that relates to reduced renal and cardiovascular complications and provides better overall survival than RN. However, whether cT1 RCCs with postoperative pT3a upstaging treated by PN have equivalent clinical survival outcomes compared with those treated by RN or not is not clear, and this interesting issue deserves to be discussed. Shah et al.  retrospectively reviewed the records of 1,250 patients who underwent PN or RN for cT1 RCC and T3a upstaging was noted in 140 patients (11%). Further subgroup analysis among upstaged T3a cases demonstrated that the risk of relapse in PN is higher than that in RN. A similar study by Jeong et al.  contradicted Shah's findings and revealed no difference in RFS between PN and RN in RCC patients with incidental pT3a upstaging. Besides, Weight et al.  analyzed the OS and CSS among patients who underwent RN or PN with cT1 and pT3 upstaging and found equivalent survivals in PN and RN groups. Moreover, Hansen et al. suggested results similar to those of Weight's study regarding the CSS among RCC patients with pT3a disease. Previous relevant studies provided inconsistent findings but the majority agreed that PN could provide at least equivocal oncological outcomes in patients with cT1/pT3a RCC. Our results showed that the incidence of upstaging was relatively unusual (5.5%). Thus, the majority of patients will still benefit from PN. Therefore, clinicians should not avoid PN because of concerns regarding upstaging, although cautious follow-up is warranted in cases with upstaging.
Our meta-analysis with large samples confirmed that patients with pathological T3a-upstaged cT1 RCC had worse clinical oncological outcomes than patients with non-upstaged cT1 RCC. Therefore, the predictors of upstaging, which might greatly aid in the preoperative counseling of patients regarding the risk of pT3a, must be considered before RCC treatment. Thus far, a series of studies has focused on this topic. Lee et al.  found that patient age, tumor diameter, and hilar location were significantly associated with a risk of pathological upstaging. Nayak et al.  showed that increasing age and tumor size were independent predictors and found that Fuhrman grade, when assessed preoperatively by a biopsy, is another predictor and might be helpful in determining the probability of upstaging. This finding is consistent with consistent with the findings of Jeongs'  and Ghanie's . Furthermore, a high R.E.N.A.L. nephrometry score has been recognized by several studies to be an important factor associated with tumor up-staging [25, 32, 33]. These factors might predict upstaging preoperatively and provide valuable adjunct information about risk stratification. Furthermore, aggressive management strategies, such as removing fat with the tumor and avoiding take an enucleation approach, can be offered to patients who are most likely to be upstaged.
Postoperative T3a upstaging has a significantly negative impact on survival outcomes, especially the RFS, of patients with cT1 RCC. Thus, these high-risk patients should be closely monitored by clinicians and should receive close follow-up. Moreover, the utility of adjuvant systemic therapies in patients with increased risk of recurrence has attracted some attention and has been discussed in recent years [34-37]. A randomized, double-blind, Phase III trial (S-TRAC)  was performed to determine the efficacy of sunitinib in patients with loco-regional RCC at high risk for tumor recurrence after nephrectomy. The results showed that the median duration of disease-free survival was significantly longer in the sunitinib group than in the placebo group. Another Phase III Trial (PROTECT)  demonstrated increased disease-free survival outcome in locally advanced renal cell carcinoma patients receiving adjuvant pazopanib. These studies emphasize the potential benefit of target therapy in select patients, and further studies specifically designed to evaluate patients with cT1 and pT3a upstaging are required to confirm the efficacy.
To the best of our knowledge, our study is the first standard meta-analysis that assessed the association between pT3a upstaging and survivals of cT1 RCC. Our systematic review of nine published studies (ten cohorts) including more than 10,000 samples indicated that the postoperative pT3a upstaging of cT1 RCC was unusual (5.5%). However, its prognostic value should not be ignored because the accurate evaluation of prognosis, especially after surgery, is highly important for the planning of surveillance program and the following relevant adjuvant therapy. Our results quantified the impact of pT3a upstaging to be a negative prognostic factor. However, several limitations of this study must also be acknowledged. First, most of these eligible studies in this systematic review were retrospective studies. Second, among the enrolled studies, some studies did not provide HRs directly and were calculated using the methods reported by Tierney et al.  These calculated HRs might not be as dependable as those retrieved directly from reported results. Third, the influence of different subtypes of T3a upstaging (renal sinus fat or perirenal fat invasion or renal vein thrombosis) on survival outcomes was not discussed owing to insufficient data. Besides, only four cohorts investigated the CSS of cT1 RCC by a comprehensive literature search, thereby probably increasing the risk of random error. Therefore, additional well-designed studies are still required to further confirm our finding. Finally, the unavoidable limitations exist. The results of all meta-analysis were affected by the quality of component studies. The situation wherein studies with insignificant results are more difficult to publish in journals than those with statistically significant results may compromise the validity of the meta-analysis .
In summary, our meta-analysis of current available evidences strongly indicates that postoperative pT3a upstaging is significantly associated with poor RFS, OS, and CSS in patients with cT1 RCC. For patients with pT3a upstaging, close monitoring and follow ups are required. Several promising upstaging predictors can provide valuable information to clinicians, and adjuvant target therapy might benefit these high-risk patients but still require further evaluation.
This work was supported by Science and Technology Research Project of Education Department of Jiangxi Province (GJJ170011).
LC and BF designed the research; LC, WD and XL performed the literature search; LC and GW analyzed the data and interpreted the results; LC and BF wrote the paper; all authors approved the final manuscript.
The authors have declared that no competing interest exists.
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Corresponding author: Prof. Bin Fu, Department of Urology, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China. Tel: +86-0791-88698102; Fax: +86-0791-88698102; E-mail: urofbinncu.edu.cn