Next Article in Journal
The Diagnostic Yield and Implications of Targeted Founder Pathogenic Variant Testing in an Israeli Cohort
Next Article in Special Issue
Non-Metastatic Clear Cell Renal Cell Carcinoma Immune Cell Infiltration Heterogeneity and Prognostic Ability in Patients Following Surgery
Previous Article in Journal
COVID-19 in Patients with Melanoma: A Single-Institution Study
Previous Article in Special Issue
Disturbances in Nitric Oxide Cycle and Related Molecular Pathways in Clear Cell Renal Cell Carcinoma
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Surgical Trends and Complications in Partial and Radical Nephrectomy: Results from the GRAND Study

Department of Urology, LMU University Hospital, LMU Munich, 81377 Munich, Germany
*
Author to whom correspondence should be addressed.
Cancers 2024, 16(1), 97; https://doi.org/10.3390/cancers16010097
Submission received: 7 December 2023 / Revised: 20 December 2023 / Accepted: 22 December 2023 / Published: 24 December 2023
(This article belongs to the Collection Clear Cell Renal Cell Carcinoma 2022–2023)

Abstract

:

Simple Summary

Studies about the current trends in renal cancer surgery and its perioperative outcomes are lacking. Using the nationwide data of Germany from 2005 to 2021, we found that the utilization of partial nephrectomy substantially increased, while the utilization of radical nephrectomy substantially decreased in the last years. Patients selected for radical nephrectomy had more comorbidities and risk factors compared to patients selected for partial nephrectomy. Our analyses suggest that patients undergoing radical nephrectomy present worse perioperative morbidity and mortality, as well as prolonged hospitalization, compared to patients undergoing partial nephrectomy.

Abstract

Background: We aimed to evaluate the current trends in renal cancer surgery, as well as to compare the perioperative outcomes of partial versus radical nephrectomy. Methods: We used the GeRmAn Nationwide inpatient Data (GRAND), provided by the Research Data Center of the Federal Bureau of Statistics (2005–2021). We report the largest study in the field, with 317,843 patients and multiple patient-level analyses. Results: Overall, 123,924 (39%) patients underwent partial and 193,919 (61%) underwent radical nephrectomy in Germany from 2005 to 2021. Of them, 57,308 (18%) were operated on in low-, 142,702 (45%) in intermediate-, and 117,833 (37%) in high-volume centers. A total of 249,333 (78%) patients underwent open, 44,994 (14%) laparoscopic, and 23,516 (8%) robotic nephrectomy. The number of patients undergoing renal surgery remained relatively stable from 2005 to 2021. Over the study period, the utilization of partial nephrectomy increased threefold, while radical nephrectomy decreased by about 40%. After adjusting for major risk factors in the multivariate regression analysis, radical nephrectomy was associated with 3.2-fold higher odds (95% CI: 3.2 to 3.9, p < 0.001) of 30-day mortality, longer hospitalization by 1.9 days (95% CI: 1.9 to 2, p < 0.001), and higher inpatient costs by EUR 1778 (95% CI: 1694 to 1862, p < 0.001) compared to partial nephrectomy. Furthermore, radical nephrectomy had a higher risk of in-hospital transfusion (p < 0.001), sepsis (p < 0.001), acute respiratory failure (p < 0.001), acute kidney disease (p < 0.001), acute thromboembolism (p < 0.001), surgical wound infection (p < 0.001), ileus (p < 0.001), intensive care unit admission (p < 0.001), and pancreatitis (p < 0.001). Conclusions: More patients are offered partial nephrectomy in Germany. Patients undergoing radical nephrectomy present with a higher rate of concomitant risk factors and have increased perioperative morbidity and mortality, prolonged hospitalization, and increased in-hospital costs.

1. Introduction

Renal cancer accounts for over 3% of all new cancer cases worldwide, affecting more than 430,000 individuals every year [1]. The increasing prevalence of risk factors for renal cancer, such as obesity, hypertension, and chronic renal disease, has contributed to a rising incidence of renal cancer globally [2]. Accordingly, the recent technological improvements, in combination with the wide implementation of cross-sectional imaging, have led to earlier diagnosis of renal cancer in many patients [3]. Therefore, 75% of all newly diagnosed renal masses are asymptomatic, incidental findings and smaller than 7 cm in diameter. About 80% of all surgically resected renal tumors are malignant in the final histology [4].
Despite the recent advancements in other local or systemic therapies, partial nephrectomy is considered the standard treatment for patients with suspected renal cancer, if technically feasible [5,6]. Partial nephrectomy has supplanted radical nephrectomy as the preferred treatment modality, given that it is associated with superior functional and equivalent oncological outcomes [7]. Radical nephrectomy remains the treatment of choice for tumors in which partial nephrectomy is not possible [8]. Both partial and radical nephrectomy can be performed with either an open or a minimally invasive approach [9]. Nevertheless, nephrectomy is associated with perioperative mortality and morbidity, as well as with prolonged hospital stay, intensive care unit admission, and significant treatment-related costs [10,11].
Currently, there is a global trend toward the centralization of complex urological operations in healthcare systems [12]. This shift is supported by the accumulating evidence indicating that increased annual hospital volume leads to improved perioperative outcomes for major urological operations. [13]. Therefore, the EAU Guideline Panel on Renal Cell Carcinoma recommends that hospitals should annually perform at least forty partial nephrectomies [14]. Nevertheless, this recommendation is based on a low level of evidence derived from retrospective studies with relatively low numbers of included patients. Indeed, there is a paucity of existing studies attempting to identify a hospital volume threshold for annual kidney cancer surgery cases that may improve perioperative outcomes. Similarly, studies assessing the perioperative complications in patients undergoing kidney cancer surgery are lacking. In this scope, we aimed to evaluate the current trends in partial and radical nephrectomy, and to compare the perioperative outcomes of partial versus radical nephrectomy through the largest study in the field.

2. Methods

2.1. GeRmAn Nationwide Inpatient Data (GRAND)

For the present analysis, we used the GeRmAn Nationwide inpatient Data (GRAND). The GRAND study contains all German inpatient data from 2005 to 2021 apart from military, psychiatric, and forensic cases. These data are stored in an anonymized format at the Research Data Center of the German Bureau of Statistics, and they were retrieved for further analysis upon agreement (LMU—4710-2022). To ensure anonymity, the Research Data Center excludes patient groups with fewer than three baseline characteristics or inpatient complications and does not allow hospital-level comparisons for any outcome. After the 2004 implementation of a diagnosis- and procedure-related remuneration system in Germany (German diagnosis-related groups (DRGs)), all hospitals need to transfer the in-hospital patient data (e.g., coexisting conditions, surgical procedures, perioperative outcomes) to the Institute for the Hospital Remuneration System to receive their remuneration. These patient data are coded based on the International Statistical Classification of Diseases and Related Health Problems, 10th revision, German modification (ICD-10-GM) and the German Procedure Classification (OPS).

2.2. Selection Criteria

We included all patients undergoing radical (OPS code: 5-554.4, 5-554.a) and partial nephrectomy (OPS code: 5-553) for suspected renal tumors. To obtain patient data on procedures, concurrent conditions, and inpatient complications, we used the available diagnostic and procedural codes (ICD-10-GM and OPS). The primary outcome of the present analysis was to assess surgical trends in patients undergoing radical or partial nephrectomy. Secondary outcomes included the effects of radical versus partial nephrectomy on 30-day mortality and perioperative complications (i.e., transfusion, sepsis, acute respiratory failure, acute kidney disease, acute thromboembolism, surgical wound infection, ileus, intensive care unit admission, and pancreatitis). We also analyzed hospital revenues and length of hospital stay. Moreover, we compared 30-day mortality and perioperative complications in patients undergoing radical versus partial nephrectomy separately in high-, intermediate-, and low-volume centers. Given that there is no consensus on the definition of high-volume centers, we defined high-volume centers as those that perform at least 100 nephrectomies (partial and radical) per year. Similarly, intermediate-volume centers were defined as those that perform between 40 and 99 nephrectomies per year, and low-volume centers were defined as those that perform less than 40 nephrectomies per year.

2.3. Data Synthesis and Statistical Analysis

Our research team did not have direct access to patient-level data. Thus, all statistical analyses were performed on our behalf by the Research Data Center of the German Bureau of Statistics, based on R codes developed by our research team (source: Research Data Center of the Federal Bureau of Statistics, DRG Statistics 2005–2021; own calculations). Subsequently, the summary results were provided to our research group for further evaluation. Approval by an ethics committee or informed patient consent was not required based on the German legislation.
All hospitals performing renal surgeries were identified through their postal codes and were further subclassified based on their annual caseload as low-volume centers (<40 cases/year), intermediate-volume centers fulfilling the EAU recommendation (40–99 cases/year), and high-volume centers (≥100 cases/year). The corresponding comparisons among low- (<40 cases/year), intermediate- (40–99 cases/year), and high-volume centers (≥100 cases/year) were performed with the chi-squared test and the Kruskal–Wallis test. Accordingly, all comparisons between patients undergoing partial versus radical nephrectomy were performed with the chi-squared test and the Mann–Whitney U test. All continuous variables were calculated as medians with interquartile ranges (IQRs), and all categorical variables were calculated as frequencies with proportions.
We conducted multiple multivariable logistic and linear regression analyses to evaluate the effect of the type of surgery and the effect of the annual hospital caseload on inpatient outcomes (i.e., 30-day mortality, perioperative complications, length of hospital stay, and hospital revenues). All regression models were adjusted for sex, age, obesity, history of chronic obstructive pulmonary disease, chronic heart failure, chronic kidney disease, cerebrovascular accident, hypertension, and diabetes, as well as for the surgical approach and the year of operation. Odds ratios (ORs) with 95% confidence intervals (CIs) were estimated for all logistic models, and two-sided p-values lower than 0.05 were considered statistically significant. The log-rank test with Kaplan–Meier analyses was used to assess the effects of radical versus partial nephrectomy on 30-day mortality.

3. Results

3.1. Baseline Characteristics

A total of 317,843 patients with a median age of 66 years (IQR: 56–74) underwent kidney cancer surgery, with 188,123 (59%) being male; 179,386 (56%) had hypertension, 65,605 (21%) has chronic kidney disease, and 57,155 (18%) had diabetes. Overall, 123,924 (39%) patients underwent partial and 193,919 (61%) underwent radical nephrectomy. A total of 249,333 (78%) patients underwent open, 44,994 (14%) laparoscopic, and 23,516 (7.4%) robotic nephrectomy. Based on the annual hospital caseload volume for kidney cancer surgery, 57,308 (18%) operations (17,108 (30%) partial and 40,200 (70%) radical nephrectomies) were performed in low-volume centers, 142,702 (45%) operations (52,966 (37%) partial and 89,736 (63%) radical nephrectomies) in intermediate-volume centers, and 117,833 (37%) operations (53,850 (46%) partial and 63,983 (54%) radical nephrectomies) in high-volume centers.
Patients undergoing radical nephrectomy were older (p < 0.001) and had higher proportions of diabetes (p < 0.001), chronic heart failure (p < 0.001), chronic obstructive pulmonary disease (p < 0.001), chronic kidney disease (p < 0.001), cerebrovascular disease (p < 0.001), and dementia (p < 0.001) compared to patients undergoing partial nephrectomy. Laparoscopic or robotic surgical approaches were preferred more often in patients undergoing partial nephrectomy (p < 0.001). The latter was also observed in the separate analyses for low-, intermediate-, and high-volume centers. The baseline characteristics of all patients undergoing renal surgery are presented in Table 1, and the corresponding baseline characteristics of patients operated on in low-, intermediate-, and high-volume centers are presented in the Supplementary Materials (Table S1).
The number of patients undergoing renal surgery increased moderately from 17,360 cases in 2005 to 18,686 in 2021. Interestingly, the number of patients undergoing partial nephrectomy substantially increased throughout these years, from 3358 cases in 2005 to 10,153 in 2021, while the number of patients undergoing radical nephrectomy substantially decreased throughout the same period, from 14,002 cases in 2005 to 8533 in 2021. The latter was also observed in low-, intermediate-, and high-volume centers. Nevertheless, the increase in partial nephrectomies and the decrease in radical nephrectomies were steeper in high-volume centers. In particular, in high-volume centers, 1427 (2.6%) partial nephrectomies and 4634 (7.2%) radical nephrectomies were performed in 2005, compared to 4485 (8.3%) partial nephrectomies and 2857 (4.5%) radical nephrectomies in 2021. The number of patients undergoing renal surgery was not affected during the COVID-19 pandemic. The annual trends for radical and partial nephrectomy are depicted in Figure 1, whereas the corresponding annual trends for radical and partial nephrectomy in low-, intermediate-, and high-volume centers are depicted in the Supplementary Materials (Figure S1).

3.2. Effects of Renal Surgery on Perioperative Morbidity, Mortality, Hospital Stay, and Costs

Overall, radical nephrectomy, compared to partial nephrectomy, was significantly associated with higher odds of transfusion (25% versus 12%; OR: 2, 95% CI: 1.9 to 2, p < 0.001), sepsis (3.1% versus 1%; OR: 2.6, 95% CI: 2.4 to 2.8, p < 0.001), acute respiratory failure (5.4% versus 3.6%; OR: 1.6, 95% CI: 1.5 to 1.7, p < 0.001), acute kidney disease (5.9% versus 4%; OR: 1.6, 95% CI: 1.5 to 1.7), acute thromboembolism (0.9% versus 0.5%; OR: 1.9, 95% CI: 1.7 to 2, p < 0.001), surgical wound infection (0.7% versus 0.3%; OR: 2, 95% CI: 1.8 to 2.2, p < 0.001), ileus (2% versus 1.3%; OR: 1.4, 95% CI: 1.3 to 1.5, p < 0.001), intensive care unit admission (21% versus 16%; OR: 1.2, 95% CI: 1.2 to 1.2, p < 0.001), and pancreatitis (0.3% versus 0.1%; OR: 2.1, 95% CI: 1.8 to 2.5, p < 0.001). Similarly, radical nephrectomy was associated with longer hospital stay by 1.9 days (95% CI: 1.9 to 2, p < 0.001) and higher inpatient costs by EUR 1778 (95% CI: 1694 to 1862, p < 0.001). The multivariable analysis is presented in Table 2 and Table 3. In the separate multivariable analyses of patients undergoing renal surgery in low-, intermediate-, and high-volume centers, radical nephrectomy was associated with worse perioperative outcomes compared to partial nephrectomy. The corresponding findings are presented in the Supplementary Materials (Table S2).
A total of 4202 (1.3%) in-hospital deaths were observed within 30 days of surgery. Of these, 540 (0.4%) deaths occurred among patients undergoing partial nephrectomy and 3662 (1.9%) among patients undergoing radical nephrectomy. The numbers of 30-day in-hospital deaths after partial nephrectomy were 116 (0.7%) in low-volume centers, 234 (0.4%) in intermediate-volume centers, and 190 (0.4%) in high-volume centers. Meanwhile, the numbers of 30-day in-hospital deaths after radical nephrectomy were 917 (2.3%) in low-volume centers, 1704 (1.9%) in intermediate-volume centers, and 1041 (1.6%) in high-volume centers.
Radical nephrectomy was associated with 3.5-fold higher odds (95% CI: 3.2 to 3.9, p < 0.001) of 30-day mortality compared to partial nephrectomy in the whole study population. In low-volume centers, radical nephrectomy was associated with 2.8-fold higher odds (95% CI: 2.3 to 3.5, p < 0.001) of 30-day mortality compared to partial nephrectomy. In intermediate-volume centers, radical nephrectomy was associated with 3.6-fold higher odds (95% CI: 3.1 to 4.1, p < 0.001) of 30-day mortality compared to partial nephrectomy. In high-volume centers, radical nephrectomy was associated with 3.7-fold higher odds (95% CI: 3.2 to 4.4, p < 0.001) of 30-day mortality compared to partial nephrectomy. The latter was also observed in the time-to-death analysis for the whole study population, as well as for low-, intermediate-, and high-volume centers (log-rank test for all comparisons: p < 0.001). The corresponding Kaplan–Meier analyses are presented in Figure 2 and Figure S2.

4. Discussion

The present high-volume study suggests that the annual cases of partial nephrectomy have undergone a threefold increase, while the annual cases of radical nephrectomy have undergone an important decrease of 40% in the last few years. Interestingly, the number of patients undergoing renal surgery has remained largely unchanged from 2005 to 2021. In high-volume centers, the proportion of partial to radical nephrectomies is higher compared to in intermediate- and low-volume centers. Furthermore, it seems that minimally invasive renal surgery is preferred in only a small proportion of patients requiring nephrectomy in Germany. It should be noted that patients undergoing radical nephrectomy displayed worse baseline characteristics compared to those undergoing partial nephrectomy. Nevertheless, after adjusting for these characteristics, we found that radical nephrectomy was associated with 195% higher odds of surgical wound infection, 160% higher odds of sepsis, 110% higher odds of pancreatitis, 100% higher odds of transfusion, 90% higher odds of acute thromboembolism, 60% higher odds of acute respiratory failure and acute kidney disease, 40% higher odds of ileus, and 20% higher odds of intensive care unit admission. Similarly, radical nephrectomy, compared to partial nephrectomy, was associated with 250% higher odds of 30-day in-hospital mortality, as well as with longer hospital stay and higher inpatient costs. The latter was also observed in the separate analysis between partial and radical nephrectomy in low-, intermediate-, and high-volume centers.
Our findings demonstrate that the utilization of partial nephrectomy has considerably increased in recent years. The latter might be predominantly attributed to the fact that current major guidelines recommend partial nephrectomy over radical nephrectomy whenever possible [14,15,16]. Studies from the US and the UK are in line with our findings demonstrating that the use of partial nephrectomy has increased significantly over time for both small and larger renal masses [17,18,19]. A large prospective study from Singapore suggested a shift towards nephron-sparing surgery for clinically localized tumors [20]. Accordingly, a nationwide study from the Netherlands demonstrated a clear increase in nephron-sparing management either with active surveillance, partial nephrectomy, or focal therapy over time for cT1a tumors. Conversely, for cT1b tumors, radical nephrectomy remained the most common treatment modality, although patients in high-volume centers more often underwent partial nephrectomy [21].
Still, despite the advancements in surgical techniques for nephrectomy, it seems that, in Germany, minimally invasive radical or partial nephrectomy is performed in a relatively small amount of patients compared to the US [22,23]. Even though the number of suspicious renal masses diagnosed every year in Germany has increased [24], the overall number of nephrectomy cases that are performed every year has remained stable in recent years [25,26]. The latter might be explained by the fact that an increasing number of patients with diagnosed renal masses undergo active surveillance or other ablative techniques [27,28,29,30]. Moreover, the fact that partial nephrectomy cases have increased by 300% while radical nephrectomy cases have decreased by 40% over the years might indicate that renal cancer is often diagnosed at less-advanced tumor stages. Indeed, large epidemiological studies suggest that the incidence of renal cancer continues to rise, mainly for early-stage tumors, whereas that of advanced stages has declined [31,32].
It should be highlighted that renal cancer surgery is associated with low in-hospital mortality and morbidity, which are higher in patients undergoing radical nephrectomy. Large prospective comparative studies indicate that in patients with similar renal masses in terms of diameter and location, partial and radical nephrectomy present comparable perioperative outcomes [8,33,34]. Still, in the present analysis, we could not perform an adjustment between the two groups in terms of their tumor characteristics. Based on the previous notion, patients undergoing radical nephrectomy presented worse baseline parameters and worse tumor characteristics, which might be the cause of the observed higher morbidity and mortality, as well as of the prolonged hospital stay and the increased costs compared to partial nephrectomy. It should be noted that patients with larger or more advanced tumors are more likely to require radical nephrectomy. The latter introduces a selection bias in the present analysis, since the inherent differences in tumor characteristics, the stage of the tumor, and patients’ general condition may impact the estimated differences in terms of outcomes when comparing partial nephrectomy and radical nephrectomy.
In the absence of detailed tumor characteristics, it is difficult to determine how an advanced tumor stage might affect outcomes. In an attempt to overcome this selection bias, we adjusted for multiple important risk factors in the multivariate regression analysis. However, without specific tumor characteristics, there may be major residual confounding due to unmeasured variables related to tumor stage and extension. Nevertheless, it should be stressed that radical nephrectomy was associated with worse perioperative outcomes for all estimates in low-, intermediate-, and high-volume centers compared to partial nephrectomy.
As this report, to the best of our knowledge, is the largest study on trends and perioperative outcomes in renal cancer surgery, our data have limitations that need to be considered. First of all, our analyses were derived from retrospective administrative data and are prone to coding errors and misclassifications. Although these administrative data present a high degree of accuracy and are regularly evaluated by independent physician task forces from healthcare insurance companies, important information on renal cancer surgery is not collected. In particular, the tumor size and location, the patient’s laboratory findings, the performance of a prior renal biopsy, the operative time, and the oncological status (i.e., histology findings, TNM classification, and surgical margins) are not available in the GRAND study. Similarly, data on mortality and morbidity after hospital discharge, readmission rates and causes of reoperation, functional outcomes, and follow-up data were not collected in the GRAND study. Moreover, the GRAND study does not provide information on the decision-making process between partial and radical nephrectomy, including patient preferences. Furthermore, the degree of baseline characteristics or perioperative complications such as chronic kidney disease, sepsis, or other perioperative complications cannot be retrieved. It was also beyond the scope of the present study to assess the number of operations performed in urological versus non-urological surgical departments (e.g., general surgery, pediatric surgery). Similarly, we did not consider exploring differences in the perioperative outcomes across different patient groups (such as younger patients, patients with obesity, or those with different levels of chronic kidney disease). Finally, our analyses are restricted to data for Germany and, thus, cannot be extrapolated to other healthcare systems. Accordingly, our findings may have limited generalizability, especially if the patient population undergoing radical nephrectomy differs systematically from those undergoing partial nephrectomy in terms of tumor characteristics and patients’ general condition. Nevertheless, in an attempt to overcome these limitations, our holistic and critical approach, combined with the size and nature of the GRAND study, leads to solid conclusions.

5. Conclusions

The present high-volume, nationwide, real-world data from Germany demonstrate an increased utilization of partial nephrectomy in renal cancer surgery. In recent years, the annual cases of partial nephrectomy have exceeded those of radical nephrectomy. Only one-fourth of all patients undergoing renal surgery are treated with a minimally invasive surgical approach. Based on our findings, patients undergoing radical nephrectomy present with worse baseline characteristics and experience higher perioperative morbidity and mortality, prolonged length of hospital stay, and increased in-hospital costs compared to patients undergoing partial nephrectomy. Still, this study’s conclusions about the superiority of partial nephrectomy in terms of perioperative outcomes should be interpreted with caution, as the decision to perform radical nephrectomy might be driven by clinical factors related to an advanced tumor stage or tumor location and/or anatomical complexity.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cancers16010097/s1, Supplementary Material Table S1: Baseline characteristics in low-, intermediate- and high-volume centers performing renal surgeries; Supplementary Material Figure S1: Annual trends in low-, intermediate- and high-volume centers performing renal surgeries, Supplementary Material Table S2: Regression analysis in low-, intermediate- and high-volume centers performing renal surgeries; Supplementary Material Figure S2: 30-day survival in low-, intermediate- and high-volume centers performing renal surgeries.

Author Contributions

Conceptualization, N.P. and G.B.S.; Methodology, I.B.; Validation, T.I.; Formal Analysis, N.P. and M.S.; Resources, C.S. and M.S.; Data Curation, G.B.S.; Writing—Original Draft, N.P. and M.S.; Writing—Review and Editing, G.B.S., C.S., I.B., T.I. and A.G.; Supervision, A.G. and M.S.; Project Administration, C.S.; Funding Acquisition, C.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Institutional Review Board Statement

Ethical approval, was not required for the present study, in accordance with the national legislation and institutional requirements.

Informed Consent Statement

Written informed consent from the participants was not required for the present study, in accordance with the national legislation and institutional requirements.

Data Availability Statement

All data used in this work are stored in an anonymized fashion at the German Federal Statistical Office.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bukavina, L.; Bensalah, K.; Bray, F.; Carlo, M.; Challacombe, B.; Karam, J.A.; Kassouf, W.; Mitchell, T.; Montironi, R.; O’Brien, T.; et al. Epidemiology of Renal Cell Carcinoma: 2022 Update. Eur. Urol. 2022, 82, 529–542. [Google Scholar] [CrossRef] [PubMed]
  2. Huang, J.; Leung, D.K.-W.; Chan, E.O.-T.; Lok, V.; Leung, S.; Wong, I.; Lao, X.-Q.; Zheng, Z.-J.; Chiu, P.K.-F.; Ng, C.-F.; et al. A Global Trend Analysis of Kidney Cancer Incidence and Mortality and Their Associations with Smoking, Alcohol Consumption, and Metabolic Syndrome. Eur. Urol. Focus 2022, 8, 200–209. [Google Scholar] [CrossRef] [PubMed]
  3. Diana, P.; Klatte, T.; Amparore, D.; Bertolo, R.; Carbonara, U.; Erdem, S.; Ingels, A.; Kara, O.; Marandino, L.; Marchioni, M.; et al. Screening programs for renal cell carcinoma: A systematic review by the EAU young academic urologists renal cancer working group. World J. Urol. 2023, 41, 929–940. [Google Scholar] [CrossRef] [PubMed]
  4. Kutikov, A.; Fossett, L.K.; Ramchandani, P.; Tomaszewski, J.E.; Siegelman, E.S.; Banner, M.P.; Van Arsdalen, K.N.; Wein, A.J.; Malkowicz, S.B. Incidence of benign pathologic findings at partial nephrectomy for solitary renal mass presumed to be renal cell carcinoma on preoperative imaging. Urology 2006, 68, 737–740. [Google Scholar] [CrossRef] [PubMed]
  5. Siva, S.; Ali, M.; Correa, R.J.M.; Muacevic, A.; Ponsky, L.; Ellis, R.J.; Lo, S.S.; Onishi, H.; Swaminath, A.; McLaughlin, M.; et al. 5-year outcomes after stereotactic ablative body radiotherapy for primary renal cell carcinoma: An individual patient data meta-analysis from IROCK (the International Radiosurgery Consortium of the Kidney). Lancet Oncol. 2022, 23, 1508–1516. [Google Scholar] [CrossRef] [PubMed]
  6. Van Poppel, H.; Da Pozzo, L.; Albrecht, W.; Matveev, V.; Bono, A.; Borkowski, A.; Marechal, J.-M.; Klotz, L.; Skinner, E.; Keane, T.; et al. A Prospective randomized EORTC intergroup phase 3 study comparing the complications of elective nephron-sparing surgery and radical nephrectomy for low-stage renal cell carcinoma. Eur. Urol. 2007, 51, 1606–1615. [Google Scholar] [CrossRef]
  7. Kim, S.P.; Thompson, R.H.; Boorjian, S.A.; Weight, C.J.; Han, L.C.; Murad, M.H.; Shippee, N.D.; Erwin, P.J.; Costello, B.A.; Chow, G.K.; et al. Comparative effectiveness for survival and renal function of partial and radical nephrectomy for localized renal tumors: A systematic review and meta-analysis. J. Urol. 2012, 188, 51–57. [Google Scholar] [CrossRef]
  8. Mir, M.C.; Derweesh, I.; Porpiglia, F.; Zargar, H.; Mottrie, A.; Autorino, R. Partial Nephrectomy Versus Radical Nephrectomy for Clinical T1b and T2 Renal Tumors: A Systematic Review and Meta-analysis of Comparative Studies. Eur. Urol. 2017, 71, 606–6177. [Google Scholar] [CrossRef]
  9. Crocerossa, F.; Carbonara, U.; Cantiello, F.; Marchioni, M.; Ditonno, P.; Mir, M.C.; Porpiglia, F.; Derweesh, I.; Hampton, L.J.; Damiano, R.; et al. Robot-assisted Radical Nephrectomy: A Systematic Review and Meta-analysis of Comparative Studies. Eur. Urol. 2021, 80, 428–439. [Google Scholar] [CrossRef]
  10. Sun, M.; Bianchi, M.; Trinh, Q.-D.; Abdollah, F.; Schmitges, J.; Jeldres, C.; Shariat, S.F.; Graefen, M.; Montorsi, F.; Perrotte, P.; et al. Hospital volume is a determinant of postoperative complications, blood transfusion and length of stay after radical or partial nephrectomy. J. Urol. 2012, 187, 405–410. [Google Scholar] [CrossRef]
  11. Hsu, R.C.J.; Salika, T.; Maw, J.; Lyratzopoulos, G.; Gnanapragasam, V.J.; Armitage, J.N. Influence of hospital volume on nephrectomy mortality and complications: A systematic review and meta-analysis stratified by surgical type. BMJ Open 2017, 7, e016833. [Google Scholar] [CrossRef] [PubMed]
  12. Xia, L.; Pulido, J.E.; Chelluri, R.R.; Strother, M.C.; Taylor, B.L.; Raman, J.D.; Guzzo, T.J. Hospital volume and outcomes of robot-assisted partial nephrectomy. BJU Int. 2018, 121, 900–907. [Google Scholar] [CrossRef] [PubMed]
  13. Bruins, H.M.; Veskimäe, E.; Hernández, V.; Neuzillet, Y.; Cathomas, R.; Compérat, E.M.; Cowan, N.C.; Gakis, G.; Espinós, E.L.; Lorch, A.; et al. The Importance of Hospital and Surgeon Volume as Major Determinants of Morbidity and Mortality after Radical Cystectomy for Bladder Cancer: A Systematic Review and Recommendations by the European Association of Urology Muscle-invasive and Metastatic Bladder Cancer Guideline Panel. Eur. Urol. Oncol. 2020, 3, 131–144. [Google Scholar] [PubMed]
  14. Ljungberg, B.; Albiges, L.; Abu-Ghanem, Y.; Bedke, J.; Capitanio, U.; Dabestani, S.; Fernández-Pello, S.; Giles, R.H.; Hofmann, F.; Hora, M.; et al. European Association of Urology Guidelines on Renal Cell Carcinoma: The 2022 Update. Eur. Urol. 2022, 82, 399–410. [Google Scholar] [CrossRef] [PubMed]
  15. Bjurlin, M.A.; Walter, D.; Taksler, G.B.; Huang, W.C.; Wysock, J.S.; Sivarajan, G.; Loeb, S.; Taneja, S.S.; Makarov, D.V. National trends in the utilization of partial nephrectomy before and after the establishment of AUA guidelines for the management of renal masses. Urology 2013, 82, 1283–1290. [Google Scholar] [CrossRef]
  16. Campbell, S.C.; Uzzo, R.G.; Karam, J.A.; Chang, S.S.; Clark, P.E.; Souter, L. Renal Mass and Localized Renal Cancer: Evaluation, Management, and Follow-up: AUA Guideline: Part II. J. Urol. 2021, 206, 209–218. [Google Scholar] [CrossRef]
  17. Fero, K.; Hamilton, Z.A.; Bindayi, A.; Murphy, J.D.; Derweesh, I.H. Utilization and quality outcomes of cT1a, cT1b and cT2a partial nephrectomy: Analysis of the national cancer database. BJU Int. 2018, 121, 565–574. [Google Scholar] [CrossRef]
  18. Plante, K.; Stewart, T.M.; Wang, D.; Bratslavsky, G.; Formica, M. Treatment trends, determinants, and survival of partial and radical nephrectomy for stage I renal cell carcinoma: Results from the National Cancer Data Base, 2004–2013. Int. Urol. Nephrol. 2017, 49, 1375–1381. [Google Scholar] [CrossRef]
  19. Hsu, R.C.J.; Barclay, M.; Loughran, M.A.; Lyratzopoulos, G.; Gnanapragasam, V.J.; Armitage, J.N. Time trends in service provision and survival outcomes for patients with renal cancer treated by nephrectomy in England 2000–2010. BJU Int. 2018, 122, 599–609. [Google Scholar] [CrossRef]
  20. Chen, K.; Lee, A.; Huang, H.H.; Tay, K.J.; Sim, A.; Lee, L.S.; Cheng, C.W.S.; Ng, L.G.; Ho, H.S.S.; Yuen, J.S.P. Evolving trends in the surgical management of renal masses over the past two decades: A contemporary picture from a large prospectively-maintained database. Int. J. Urol. 2019, 26, 465–474. [Google Scholar] [CrossRef]
  21. Yildirim, H.; Schuurman, M.S.; Widdershoven, C.V.; Lagerveld, B.W.; Brink, L.v.D.; Ruiter, A.E.C.; Beerlage, H.P.; van Moorselaar, R.J.A.; Graafland, N.M.; Bex, A.; et al. Variation in the management of cT1 renal cancer by surgical hospital volume: A nationwide study. BJUI Compass 2023, 4, 455–463. [Google Scholar] [CrossRef] [PubMed]
  22. Alameddine, M.; Koru-Sengul, T.; Moore, K.J.; Miao, F.; Sávio, L.F.; Nahar, B.; Prakash, N.S.; Venkatramani, V.; Jue, J.S.; Punnen, S.; et al. Trends in Utilization of Robotic and Open Partial Nephrectomy for Management of cT1 Renal Masses. Eur. Urol. Focus 2019, 5, 482–487. [Google Scholar] [CrossRef] [PubMed]
  23. Xia, L.; Talwar, R.; Taylor, B.L.; Shin, M.H.; Berger, I.B.; Sperling, C.D.; Chelluri, R.R.; Zambrano, I.A.; Raman, J.D.; Guzzo, T.J. National trends and disparities of minimally invasive surgery for localized renal cancer, 2010 to 2015. Urol. Oncol. Semin. Orig. Investig. 2019, 37, 182.e17–182.e27. [Google Scholar] [CrossRef] [PubMed]
  24. Volpe, A.; Cadeddu, J.A.; Cestari, A.; Gill, I.S.; Jewett, M.A.; Joniau, S.; Kirkali, Z.; Marberger, M.; Patard, J.J.; Staehler, M.; et al. Contemporary management of small renal masses. Eur. Urol. 2011, 60, 501–515. [Google Scholar] [CrossRef] [PubMed]
  25. Ferlay, J.; Colombet, M.; Soerjomataram, I.; Parkin, D.M.; Piñeros, M.; Znaor, A.; Bray, F. Cancer statistics for the year 2020: An overview. Int. J. Cancer 2021, 149, 778–789. [Google Scholar] [CrossRef] [PubMed]
  26. Ferlay, J.; Steliarova-Foucher, E.; Lortet-Tieulent, J.; Rosso, S.; Coebergh, J.W.W.; Comber, H.; Forman, D.; Bray, F. Cancer incidence and mortality patterns in Europe: Estimates for 40 countries in 2012. Eur. J. Cancer 2013, 49, 1374–1403. [Google Scholar] [CrossRef] [PubMed]
  27. Palumbo, C.; A Mistretta, F.; Knipper, S.; Mazzone, E.; Pecoraro, A.; Tian, Z.; Perrotte, P.; Antonelli, A.; Montorsi, F.; Shariat, S.F.; et al. Assessment of local tumor ablation and non-interventional management versus partial nephrectomy in T1a renal cell carcinoma. Minerva Urol. Nefrol. 2020, 72, 350–359. [Google Scholar] [CrossRef]
  28. Su, Z.T.; Patel, H.D.; Huang, M.M.; Alam, R.; Cheaib, J.G.; Pavlovich, C.P.; Allaf, M.E.; Pierorazio, P.M. Active Surveillance versus Immediate Intervention for Small Renal Masses: A Cost-Effectiveness and Clinical Decision Analysis. J. Urol. 2022, 208, 794–803. [Google Scholar] [CrossRef]
  29. Correa, R.J.; Louie, A.V.; Zaorsky, N.G.; Lehrer, E.J.; Ellis, R.; Ponsky, L.; Kaplan, I.; Mahadevan, A.; Chu, W.; Swaminath, A.; et al. The Emerging Role of Stereotactic Ablative Radiotherapy for Primary Renal Cell Carcinoma: A Systematic Review and Meta-Analysis. Eur. Urol. Focus 2019, 5, 958–969. [Google Scholar] [CrossRef]
  30. Flegar, L.; Thoduka, S.G.; Mahnken, A.H.; Figiel, J.; Heers, H.; Aksoy, C.; Eisenmenger, N.; Groeben, C.; Huber, J.; Zacharis, A. Focal Therapy for Renal Cancer: Comparative Trends in the USA and Germany from 2006 to 2020 and Analysis of the German Health Care Landscape. Urol. Int. 2023, 107, 396–405. [Google Scholar] [CrossRef]
  31. Znaor, A.; Lortet-Tieulent, J.; Laversanne, M.; Jemal, A.; Bray, F. International variations and trends in renal cell carcinoma incidence and mortality. Eur. Urol. 2015, 67, 519–530. [Google Scholar] [CrossRef] [PubMed]
  32. Chow, W.-H.; Dong, L.M.; Devesa, S.S. Epidemiology and risk factors for kidney cancer. Nat. Rev. Urol. 2010, 7, 245–257. [Google Scholar] [CrossRef] [PubMed]
  33. Li, J.; Zhang, Y.; Teng, Z.; Han, Z. Partial nephrectomy versus radical nephrectomy for cT2 or greater renal tumors: A systematic review and meta-analysis. Minerva Urol. Nefrol. 2019, 71, 435–444. [Google Scholar] [CrossRef] [PubMed]
  34. Pierorazio, P.M.; Johnson, M.H.; Patel, H.D.; Sozio, S.M.; Sharma, R.; Iyoha, E.; Bass, E.B.; Allaf, M.E. Management of Renal Masses and Localized Renal Cancer: Systematic Review and Meta-Analysis. J. Urol. 2016, 196, 989–999. [Google Scholar] [CrossRef]
Figure 1. The annual trends for radical and partial nephrectomy.
Figure 1. The annual trends for radical and partial nephrectomy.
Cancers 16 00097 g001
Figure 2. Kaplan–Maier curve for the 30-day survival in patients undergoing radical versus partial nephrectomy.
Figure 2. Kaplan–Maier curve for the 30-day survival in patients undergoing radical versus partial nephrectomy.
Cancers 16 00097 g002
Table 1. Baseline characteristics of the included patients based on the type of renal cancer surgery: Variables are presented as medians with interquartile ranges or as frequencies with proportions. The Mann–Whitney test was performed for comparisons between continuous variables, and the chi-squared test was used for categorical variables. The bold cells indicate statistically significant p-values.
Table 1. Baseline characteristics of the included patients based on the type of renal cancer surgery: Variables are presented as medians with interquartile ranges or as frequencies with proportions. The Mann–Whitney test was performed for comparisons between continuous variables, and the chi-squared test was used for categorical variables. The bold cells indicate statistically significant p-values.
CharacteristicOverall, n = 317,843Partial Nephrectomy, n = 123,924Radical Nephrectomy, n = 193,919p-Value
Age (years)66 (56–74)65 (56–73)67 (56–75)<0.001
Males188,123 (59%)77,117 (62%)111,006 (57%)<0.001
Diabetes57,155 (18%)21,319 (17%)35,836 (18%)<0.001
Chronic heart failure20,140 (6.3%)5722 (4.6%)14,418 (7.4%)<0.001
Chronic obstructive pulmonary disease23,142 (7.3%)8694 (7%)14,448 (7.5%)<0.001
Chronic kidney disease65,605 (21%)16,380 (13%)49,225 (25%)<0.001
Cerebrovascular disease7607 (2.4%)2126 (1.7%)5481 (2.8%)<0.001
Dementia3689 (1.2%)693 (0.6%)2996 (1.5%)<0.001
Hypertension179,386 (56%)70,382 (57%)109,004 (56%)0.001
Obesity32,008 (10%)12,384 (10%)19,624 (10%)0.25
Operative technique <0.001
Open249,333 (78%)89,227 (72%)160,106 (83%)
Laparoscopic44,994 (14%)15,528 (13%)29,466 (15%)
Robotic23,516 (7.4%)19,169 (15%)4347 (2.2%)
Table 2. Multivariable logistic regression analysis for the effects of the type of surgery on transfusion, sepsis, acute respiratory failure, acute kidney disease, acute thromboembolism, and surgical wound infection. All models are adjusted for sex, age, obesity, history of chronic obstructive pulmonary disease, chronic heart failure, chronic kidney disease, cerebrovascular accident, hypertension, diabetes, surgical approach, and year of operation. The bold cells indicate statistically significant p-values. CI: confidence interval, OR: odds ratio.
Table 2. Multivariable logistic regression analysis for the effects of the type of surgery on transfusion, sepsis, acute respiratory failure, acute kidney disease, acute thromboembolism, and surgical wound infection. All models are adjusted for sex, age, obesity, history of chronic obstructive pulmonary disease, chronic heart failure, chronic kidney disease, cerebrovascular accident, hypertension, diabetes, surgical approach, and year of operation. The bold cells indicate statistically significant p-values. CI: confidence interval, OR: odds ratio.
Complications Partial NephrectomyRadical Nephrectomy
TransfusionEvents15,315 (12%)49,169 (25%)
OR (95% CI)-2 (1.9, 2)
p-Value-<0.001
SepsisEvents1260 (1%)6018 (3.1%)
OR (95% CI)-2.6 (2.4, 2.8)
p-Value-<0.001
Acute respiratory failureEvents4448 (3.6%)10,438 (5.4%)
OR (95% CI)-1.6 (1.5, 1.7)
p-Value-<0.001
Acute kidney diseaseEvents4985 (4%)11,408 (5.9%)
OR (95% CI)-1.6 (1.5, 1.7)
p-Value-<0.001
Acute thromboembolismEvents630 (0.5%)1802 (0.9%)
OR (95% CI)-1.9 (1.7, 2)
p-Value-<0.001
Surgical wound infectionEvents391 (0.3%)1369 (0.7%)
OR (95% CI)-2 (1.8, 2.2)
p-Value-<0.001
Table 3. Multivariable linear and logistic regression analysis for the effects of the type of surgery on ileus, 30-day mortality, ICU admission, length of hospital stay, costs, and pancreatitis. All models are adjusted for sex, age, obesity, history of chronic obstructive pulmonary disease, chronic heart failure, chronic kidney disease, cerebrovascular accident, hypertension, diabetes, surgical approach, and year of operation. The bold cells indicate statistically significant p-values. CI: confidence interval, ICU: intensive care unit, OR: odds ratio.
Table 3. Multivariable linear and logistic regression analysis for the effects of the type of surgery on ileus, 30-day mortality, ICU admission, length of hospital stay, costs, and pancreatitis. All models are adjusted for sex, age, obesity, history of chronic obstructive pulmonary disease, chronic heart failure, chronic kidney disease, cerebrovascular accident, hypertension, diabetes, surgical approach, and year of operation. The bold cells indicate statistically significant p-values. CI: confidence interval, ICU: intensive care unit, OR: odds ratio.
Complications Partial NephrectomyRadical Nephrectomy
IleusEvents1623 (1.3%)3903 (2%)
OR (95% CI)-1.4 (1.3, 1.5)
p-Value-<0.001
30-Day mortalityEvents540 (0.4%)3662 (1.9%)
OR (95% CI)-3.5 (3.2, 3.9)
p-Value-<0.001
ICU admissionEvents20,116 (16%)41,355 (21%)
OR (95% CI)-1.2 (1.2, 1.2)
p-Value-<0.001
Length of hospital stayDays9 (7–11)10 (8–15)
Beta (95% CI)-1.9 (1.9, 2)
p-Value-<0.001
CostsEUR7087 (6484–8122)7400 (6484–10,492)
Beta (95% CI)-1778 (1694, 1862)
p-Value-<0.001
PancreatitisEvents166 (0.1%)636 (0.3%)
OR (95% CI)-2 (1.8, 2.5)
p-Value-<0.001
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Pyrgidis, N.; Schulz, G.B.; Stief, C.; Blajan, I.; Ivanova, T.; Graser, A.; Staehler, M. Surgical Trends and Complications in Partial and Radical Nephrectomy: Results from the GRAND Study. Cancers 2024, 16, 97. https://doi.org/10.3390/cancers16010097

AMA Style

Pyrgidis N, Schulz GB, Stief C, Blajan I, Ivanova T, Graser A, Staehler M. Surgical Trends and Complications in Partial and Radical Nephrectomy: Results from the GRAND Study. Cancers. 2024; 16(1):97. https://doi.org/10.3390/cancers16010097

Chicago/Turabian Style

Pyrgidis, Nikolaos, Gerald Bastian Schulz, Christian Stief, Iulia Blajan, Troya Ivanova, Annabel Graser, and Michael Staehler. 2024. "Surgical Trends and Complications in Partial and Radical Nephrectomy: Results from the GRAND Study" Cancers 16, no. 1: 97. https://doi.org/10.3390/cancers16010097

APA Style

Pyrgidis, N., Schulz, G. B., Stief, C., Blajan, I., Ivanova, T., Graser, A., & Staehler, M. (2024). Surgical Trends and Complications in Partial and Radical Nephrectomy: Results from the GRAND Study. Cancers, 16(1), 97. https://doi.org/10.3390/cancers16010097

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