Perioperative Complications and Oncologic Outcomes after Radical Cystectomy in End-Stage Renal Disease Patients with Bladder Cancer Obtained Using a Standardized Reporting System
by
, and
Yu-Liang Liu
1, 
Chun-Te Wu
2,3,
Yu-Chao Hsu
2,3,
Miao-Fen Chen
2,4,
Chih-Shou Chen
1,2,
Chung-Sheng Shi
5 and
Yun-Ching Huang
1,2,* 1
Division of Urology, Department of Surgery, Chang Gung Memorial Hospital at Chiayi, Chiayi 613016, Taiwan
2
Department of Medicine, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan
3
Department of Urology, Chang Gung Memorial Hospital at Linkou, Taoyuan 333423, Taiwan
4
Department of Radiation Oncology, Chang Gung Memorial Hospital at Chiayi, Chiayi 613016, Taiwan
5
Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan
*
Author to whom correspondence should be addressed.
Cancers 2022, 14(14), 3512; https://doi.org/10.3390/cancers14143512
Submission received: 14 June 2022
/
Revised: 12 July 2022
/
Accepted: 18 July 2022
/
Published: 19 July 2022
(This article belongs to the Special Issue Advances and Perspectives in Diagnosis and Treatment Strategies for Bladder Cancer)
Abstract
:Simple Summary
Urothelial carcinoma (UC) of the bladder is the most common malignancy in dialysis patients in Taiwan compared with renal cell carcinoma in Western countries. Radical cystectomy is the standard of care for localized muscle-invasive bladder cancer (MIBC), as well as for selected patients with high-risk non-MIBC. Despite improvements in anesthetic competency, surgical techniques, and postoperative care, dialysis patients undergoing radical cystectomy are at a higher risk of perioperative morbidity and mortality than non-dialysis patients. Due to the relative rarity of the condition, published data on predictors of outcome in ESRD patients undergoing radical cystectomy are scant. Our study revealed that accurate reporting of complications is necessary for preoperative counseling, identifying modifiable risk factors, and planning risk mitigation strategies. High comorbidity and low-volume surgeons were interrelated as notable risk factors for major complications. In addition to tumor-related factors, male sex, older age, and major complications significantly influence survival.
Abstract
Background: We investigated the use of a standardized reporting system to study perioperative complications and oncologic outcomes after radical cystectomy in end-stage renal disease (ESRD) patients with bladder cancer. Methods: We reviewed retrospective outcomes in 141 ESRD patients with bladder cancer who underwent radical cystectomy between 2004 and 2015. Complications were graded using the Clavien–Dindo classification system with 0–2 classified as “No Major Complications” and Clavien 3–5 as “Major Complications”. Low-volume surgeons were classified as those performing fewer than nine cases during the study. Fisher’s exact test along with the chi-squared test, two-tailed t tests, logistic regression, and the Cox proportional hazard model were used to evaluate all clinically meaningful covariates. Results: Ninety-nine (99, 70.2%) patients had no major complications, and forty-two (29.8%) patients had major complications. Patients in the major complications group were older, had a higher Charlson comorbidity index (CCI), and had a longer hospitalization duration than those in the no major complications group (all, p < 0.05). Major complications were also more common when the procedure was performed by low-volume surgeons (p = 0.003). In multivariate logistic regression models, CCI ≥ 5 (p = 0.006) and low-volume surgeon (p = 0.004) were independent predictors of major complications. According to multivariate analysis with the Cox hazards regression, male sex, age > 70 years, CCI ≥ 5, bladder cancer stage ≥ 3, lymphovascular invasion, and experiencing major complications were significant poor prognostic factors for overall survival (all, p < 0.05). Conclusions: Accurate reporting of complications is necessary for preoperative counseling, identifying modifiable risk factors, and planning risk mitigation strategies. High comorbidity and low-volume surgeons were interrelated as notable risk factors for major complications. In addition to tumor-related factors, male sex, older age, and major complications significantly influence overall survival.
Keywords:
complication; cystectomy; bladder; cancer; urothelial carcinoma; end-stage renal disease; dialysis1. Introduction
Chronic kidney disease (CKD) is a substantial public health concern worldwide, with CKD stage 3–5 estimated to affect 11–13% of the general population [1]. Taiwan has the highest prevalence (3679 per million population in 2019) and the second-highest incidence (529 new cases per million population in 2019) of treated end-stage renal disease (ESRD) in the world [2]. ESRD patients on dialysis have an elevated incidence of certain cancers and death compared with the general population [3]. In Taiwan, urothelial carcinoma (UC) of the bladder is the most common malignancy in patients receiving dialysis [4].
Dialysis patients with bladder UC are more likely to have synchronous or metachronous cancer foci throughout the urinary tract and often present with more adverse pathologic features than non-dialysis patients. Radical cystectomy is the standard of care for localized muscle-invasive bladder cancer (MIBC), as well as for selected patients with high-risk non-MIBC (NMIBC), regardless of ESRD status [5]. Despite improvements in anesthetic competency, surgical techniques, and postoperative care that have reduced procedure-related complication rates, dialysis patients undergoing radical cystectomy are at a higher risk of perioperative morbidity and mortality than non-dialysis patients [6]. Sato et al. reported that the major complication rate (Clavien grades 3–5) after radical cystectomy in dialysis patients was 30%, with a mortality rate of 20% [7]. These rates are significantly higher than the 13% major complication rate and 1.5% mortality rate reported by Shabsigh et al. for the general population undergoing radical cystectomy [8]. Increased morbidity and mortality in dialysis patients may relate to a high prevalence of heart disease [9], perioperative fluid and electrolyte disturbances [10], bleeding diathesis [11], and hemodynamic instability. Although these entities are plausible explanations for the increased risk of complications, published data on predictors of outcome in ESRD patients undergoing radical cystectomy are scant.
In this study, we identify the incidence, type, and severity of perioperative complications in dialysis patients undergoing radical cystectomy for UC using a standardized complication reporting system. Our intention is to provide information to guide perioperative management and prognostication for ESRD patients contemplating radical cystectomy. Secondary endpoints include survival analysis for ESRD patients undergoing radical cystectomy. We hypothesized that known risk factors for major perioperative complications from radical cystectomy would be applicable to the ESRD population.
2. Methods
2.1. Study Population
Institutional review board (IRB) approval was obtained (IRB No. 202100779B0), and the requirement for informed consent was waived. In total, 141 patients with ESRD and comorbid bladder cancer who underwent radical cystectomy with a curative intent between January 2004 and December 2015 were identified from the medical record systems of two major cancer centers. At our institutions, radical cystectomy is recommended for dialysis patients with localized MIBC or for selected dialysis patients with recurrence or incomplete transurethral resection of NMIBC. Abdominopelvic computed tomography (CT) or magnetic resonance urography (MRU) and transurethral resection were used for preoperative staging, whereas cytology, chest CT, and bone scan were performed as indicated in select patients.
2.2. Pathological Evaluation
The final pathological features collected at the time of radical cystectomy were as follows: tumor stage, tumor grade, lymphovascular invasion (LVI, yes/no), tumor margin status (positive/negative), and presence of carcinoma in situ (CIS, yes/no). The tumor stage was determined according to the 8th edition of the American Joint Committee on Cancer TNM Staging System. For urothelial histologies, low and high grades were used to match the current World Health Organization/International Society of Urological Pathology’s recommended grading system. All specimens were evaluated by urological pathologists at our institutions.
2.3. Outcome Measures
Recommended follow-up for all patients included annual and “for cause” cross-sectional imaging (abdominopelvic CT or MRU) and chest radiography. Chest CT and bone scan were performed as indicated in select patients with advanced stage or bone pain.
The following patient, surgical, and postoperative data were collected: sex, age at surgery, body mass index (BMI), Charlson comorbidity index (CCI), prior abdominal surgery, renal replacement therapy method(s) and duration, preoperative hemoglobin, preoperative plasma potassium, year of cystectomy, American Society of Anesthesiologists (ASA) score, operative surgeon volume, operative method, operative time, intraoperative blood loss, hospitalization duration, and final pathological findings. Surgeon volume was assessed as a binary with low-volume surgeons classified as those performing < 9 cases during the study and high-volume surgeons being those with ≥ 9 cases during that interval [12].
The Clavien–Dindo classification system was used to grade surgical complications [13]. Clavien–Dindo is a standardized complication reporting system recommended by the International Consultation on Urological Diseases-European Association of Urology International Consultation on Bladder Cancer 2012 [14]. Complications were censored within the first 90 days after cystectomy or during hospitalization, whichever was longer. Major complications were classified as Clavien grades 3–5 [15]. The impact of clinical characteristics on perioperative complications was evaluated by stratifying the patients into the no major complications group (Clavien grade 0–2 complications only) and the major complications group (any Clavien grade 3–5 complications).
Survival time was calculated from the date of radical cystectomy to the time of the last follow-up or death (cancer-specific or any cause). Recurrence time was estimated from the date of radical cystectomy to the time of first recurrence (if any). Metachronous upper tract UC was not included in the recurrence-free survival analysis.
2.4. Statistical Analysis
All statistical comparisons were performed using SPSS version 20 (IBM Corporation, Armonk, NY, USA) or Prism version 9 (GraphPad Software, San Diego, CA, USA). In descriptive analyses, continuous and categorical variables were reported as median values with ranges and proportions, respectively. The two-tailed t test was used to compare the difference in continuous variables between patients who did or did not have major complications, whereas categorical variables were analyzed using Fisher’s exact test along with the chi-squared test. Univariable and multivariable logistic regressions were used to evaluate the odds ratio (OR) with a 95% confidence interval (CI) and identify factors independently associated with experiencing major complications. We used the Kaplan–Meier method with the log-rank test to analyze overall survival, cancer-specific survival, and recurrence-free survival rates after radical cystectomy. Univariate and multivariate analyses with Cox hazards regression were used to analyze the value of prognostic factors for overall, cancer-specific, and recurrence-free survival [16,17]. p < 0.05 was set as the threshold for statistical significance for all analyses. Because of sample size considerations, only those factors identified with p < 0.05 in univariable analysis were further evaluated in multivariable analysis.
3. Results
3.1. Study Population
In total, 141 patients with ESRD who received radical cystectomy during the time interval of the study were identified (Table 1). The median patient age was 64 years (range, 24–86 years).
From the study cohort, 99 (70.2%) and 42 (29.8%) patients had Clavien grade 0–2 complications (no major complications) and Clavien grade 3–5 complications (major complications), respectively. Female patients (59.6%) were slightly predominant in both groups. Patients in the major complications group were older (70 vs. 63 years, p = 0.010), had a higher CCI (5 vs. 4, p = 0.003), and had a longer hospitalization duration (14 vs. 9 days, p < 0.001) than patients in the no major complications group. The procedure was performed by 27 surgeons, and the median surgeon volume was 3 cases (range, 1–27 cases) during the time interval of the study. Major complication rates were higher when the procedure was performed by low-volume surgeons (<9 cases; p = 0.003). None of the other variables analyzed showed a statistically significant difference between groups (all, p > 0.05).
3.2. Pathological Features
In the study population, one (0.7%) patient had small cell neuroendocrine carcinoma, and two (1.4%) patients had adenocarcinoma, with the remainder having UC. A substantial minority of patients (52, 36.9%) had no residual tumor at radical cystectomy; all of these had a history of bladder cancer previously treated by transurethral resection (median, two procedures; range, one to nine procedures, Table 2). The pathological stage of the radical cystectomy specimen was MIBC in 26 (18.4%) patients, suggesting that most patients underwent the procedure for recurrent disease or incomplete transurethral resection of NMIBC. Among the 57 male patients, prostate cancer was diagnosed in 12 (21.1%) patients at radical cystoprostatectomy.
No statistically significant difference in tumor stage, tumor grade, LVI, positive surgical margin, and CIS was noted between patients who did or did not have major complications (all, p > 0.05).
3.3. Postoperative Complications
Overall, 116 (82.3%) patients experienced one or more complications. Of them, 42 (29.8%) patients had major complications (Table 3). Arteriovenous shunt dysfunction requiring surgical intervention was the most common major complication, affecting 10 (7.1%) patients. No intraoperative death was noted. Seven (7, 5.0%) patients died in the postoperative recovery period. The causes of death were intra-abdominal abscess (n = 3), cardiac arrest (n = 2), acute respiratory distress syndrome (n = 1), and pancreatic injury (n = 1). Median time to death for the seven patients was 8 days after surgery (range, 2–145 days).
3.4. Predictive Probability of Major Complications
Categorically coded age > 70 years (OR, 2.77, 95% CI, 1.17–6.56; p = 0.020), CCI ≥ 5 (OR, 3.54, 95% CI, 1.57–7.98; p = 0.002), surgeon volume < 9 cases (OR, 3.29, 95% CI, 1.55–6.99; p = 0.002), and LVI (OR, 3.96, 95% CI, 1.06–14.8; p = 0.041) were independent predictors of postoperative major complications in univariate logistic regression analyses (Table 4). According to the results of multivariate analyses, only CCI ≥ 5 (OR, 3.43, 95% CI, 1.43–8.23; p = 0.006) and low-volume surgeon (OR, 3.29, 95% CI, 1.46–7.40; p = 0.004) were independently associated with major complications. No variable was significantly predictive of perioperative mortality after multivariable adjustment (data not shown).
3.5. Recurrence and Survival
The median follow-up period after radical cystectomy was 50.7 months (range, 2 days to 179.6 months, Table 5). At the end of follow-up, 7 (5.0%) patients died of perioperative complications, 7 (5.0%) died of bladder cancer-associated causes, and 24 (17.0%) died of other causes. Bladder cancer recurrence was detected in 15 (10.6%) patients. The 5-year overall, cancer-specific, and recurrence-free survival rates were 76.0%, 93.0%, and 86.8%, respectively.
Categorically coded male sex (HR 2.36, 95% CI, 1.15–4.83; p = 0.019), age > 70 years (HR 2.91, 95% CI, 1.29–6.60; p = 0.010), CCI ≥ 5 (HR 4.03, 95% CI, 1.54–10.5; p = 0.004), bladder cancer stage ≥ 3 (HR 37.2, 95% CI, 6.44–215; p < 0.001), LVI (HR 0.1, 95% CI, 0.01–0.76; p = 0.026), and Clavien grade 3–5 complications (HR 3.58, 95% CI, 1.61–7.95; p = 0.002) were significant negative prognostic factors for overall survival in the multivariable Cox regression models. In addition, bladder cancer stage ≥ 3 (HR 6.61, 95% CI, 1.04–42.1; p = 0.046) and kidney transplantation (HR 6.75, 95% CI 1.09–41.7; p = 0.040) in multivariable analysis were the only significant unfavorable prognostic factors for cancer-specific and recurrence-free survival, respectively.
4. Discussion
Although many risk factors have been described and validated to help predict radical cystectomy-associated complications in the general population, information regarding perioperative complications and survival in dialysis patients with UC undergoing radical cystectomy is less and limited to small case series [7,18,19]. In the largest study using administrative data from the United States Renal Data System database, Johnson et al. identified 985 hemodialysis patients receiving radical cystectomy from different centers [20]. In these patients, surgical morbidity and mortality were significant, and 5-year overall survival was low. Notably, in that study, staging information and specific operative details were unavailable, and the complication was not reported using a standardized reporting methodology. Although our current study is not a multi-institutional collaborative study, patient care, including surgery and postoperative care, was uniform at our institutions. Furthermore, surgical complications were strictly reported according to the standardized reporting system, and survival rates were accurately recorded.
The ASA score, introduced in 1941 and originally designed to standardize patients’ physical status categories for statistical studies and for hospital records, is most frequently reported as a general surgical risk score [21]. The ASA score is a useful classification system but is limited by interobserver variability; a cohort of anesthesiologists may ascribe different ASA scores to the same patient [22]. In contrast to the ASA score, the CCI stratifies comorbidity into different risk groups by more precisely assigning scores to various illnesses, which consists of 19 clinically critical conditions with each given 1–6 points based on a low or high morbidity grade [23]. Although both CCI and ASA scores are common indicators of the methodology used to assess patient risk stratification, in our cohort, only CCI was significantly beneficial in predicting perioperative major complications after radical cystectomy rather than ASA score. Very similar results were reported by Yuh et al.; CCI (OR, 1.39, 95% CI, 1.10–1.76; p = 0.007), preoperative hematocrit (OR, 2.62, 95% CI, 1.19–5.78; p = 0.02), and neobladder diversion (OR, 3.01, 95% CI, 1.21–7.52; p = 0.02) in multivariable analysis were the only significant predictors of major complications [24]. Many studies have reported a correlation between major complications and the ASA score [25,26,27]. We acknowledge that an association between ASA and morbidity may not have been apparent in our data since 92.2% patients in our study had an ASA score of 3.
Existing studies have documented the effects of hospital volume on cystectomy outcomes in the general population; however, limited and conflicting data are available regarding surgeon volume [5,28]. To the best of our knowledge, the impact of surgeon volume on the prediction of complications in dialysis patients undergoing radical cystectomy has not been corroborated. In our multivariate logistic regression model, in-hospital major complications were less frequent when the procedure was performed by a high-volume surgeon (≥9 cases during the study) than by a low-volume surgeon (<9 cases during the study). This finding adds further credence to the notion that radical cystectomy candidates are best served by referrals to high-volume surgeons working in specialized centers.
The 5-year cancer-specific survival rate in our series was 93.0%, slightly higher than that in other contemporary studies (29.5–80.3%) [20,29]. The reasons for enhanced cancer-specific survival in these patients are unclear, but several potential explanations are available. First, the single-payer national health insurance system in Taiwan provides universal health coverage to >99% of Taiwan’s population and covers 92.6% of all hospitals, clinics, and other healthcare facilities [30]. Patients in Taiwan are not restricted in terms of their healthcare access. Second, due to the high incidence of upper or lower urinary tract UC in dialysis patients in Taiwan [31], these patients are under the strict medical surveillance of healthcare facilities and have frequent contact with their clinicians, especially when they develop signs concerning recurrent disease. In addition, dialysis patients tend to have pathologically more advanced bladder cancers, often necessitating radical cystectomy and exhibiting a poor prognosis, as reported in other collaborative reports [7,19]. However, in our current study, most patients receiving radical cystectomy had NMIBC (81.6%), implying a less aggressive variant.
Patients with ESRD have an elevated risk of site-specific cancer incidence and cancer death compared with people without ESRD, but over half of the known deaths were related to cardiovascular diseases [32]. In patients with ESRD receiving hemodialysis, the percentage of deaths attributable to cancer appears to be relatively low, accounting for 2.9% of deaths among patients with a known cause from the United States Renal Data System 2021 Annual Data Report [2]. Similarly, in this study, only 7 (5.0%) patients died of bladder cancer-associated causes compared with 24 (17.0%) patients who died of all other causes. Many risk factors unrelated to the dialysis procedure are associated with decreased survival among dialysis patients, including age, race, country, smoking, comorbidities, nutritional status, laboratory test, underlying cause of ESRD, performance status, psychosocial factors, salt intake, residual renal function, pre-dialysis care, and compliance [33]. Our multivariate model showed that age > 70 years and CCI ≥ 5 are significant unfavorable prognostic factors for decreased overall survival. Similarly, in Noh et al.’s study, age ≥ 70.5 years and modified CCI > 4 were the best predictors of mortality in dialysis patients, and survival HR was predicted as 4.61 compared with the overall study population [34].
Unlike other predictive factors, the effects of sex on all-cause mortality in dialysis patients have rarely been discussed. Although the reasons for the higher death rates in male patients undergoing dialysis are incompletely understood, life expectancy at birth in Taiwan was generally lower for men (76.7 years, 95% uncertainty intervals 75.0–78.5) than for women (82.8 years, 95% uncertainty intervals 81.4–84.4) in 2016 [35]. The findings are similar to those of the reports of the National Health Insurance Research Database, according to which the mortality rate of ESRD patients in Taiwan is slightly higher in men than in women at 11.1 and 10.2 deaths per hundred patient-years, respectively [36,37]. Nevertheless, the relationships between mortality and sex in dialysis patients require further investigation.
Although kidney transplantation is considered the treatment of choice in dialysis patients with UC who are cancer-free for more than 2 years after surgery, kidney transplantation recipients are known to have a higher cancer recurrence rate than the general population [38]. In our multivariate analysis, kidney transplantation was an independent predictor of subsequent cancer recurrence. Multiple factors, including genetic background, environmental factors, underlying cause of ESRD, and immunosuppressive status, may contribute to the recurrence of malignancy. Moreover, 13 of 141 (9.2%) patients had bladder cancer stage 3 or 4 compared with 2 of 4 (50%) patients receiving kidney transplantation in the current study. These data suggest that renal transplant recipients had a higher rate of being diagnosed with more advanced bladder cancer. Therefore, we recommend using the lowest possible dose of immunosuppressive agents and more rigorous medical surveillance in kidney transplant recipients developing cancers.
This is a relatively large study focusing on complications and outcomes classified according to a standardized system in a clinically challenging patient population. We acknowledge several limitations. First, this is a retrospective, nonrandomized controlled study. Selection bias is inevitable, as radical cystectomy in patients with NMIBC was chosen depending on patient preference after discussion with the treating urologist and anesthesiologist. Second, a control group is lacking. To determine the predictors of major complications and potential prognostic factors for survival, categorization of variables may result in overfitting of predictive and prognostic models. Additionally, the number of patients is too small to draw definite conclusions, especially in the major complications group. Prospective, large-scale trials are required to best determine how to optimize care for ESRD patients with UC.
5. Conclusions
Accurate reporting of complications is essential for preoperative counseling, identifying modifiable risk factors to reduce complication rates, and planning risk mitigation strategies. A high comorbidity index is associated with an increased risk of postoperative complications and reduces overall survival. Perioperative major complications may be minimized by directing patients to surgeons who frequently perform radical cystectomy. In addition to tumor-related factors, male sex, older age, and perioperative major complications have an impact on overall survival after radical cystectomy in dialysis patients with bladder cancer.
Author Contributions
Conceptualization, Y.-C.H. (Yun-Ching Huang); methodology, M.-F.C.; software, Y.-L.L. and Y.-C.H. (Yu-Chao Hsu); validation, Y.-L.L., C.-T.W., Y.-C.H. (Yu-Chao Hsu), M.-F.C., C.-S.C., and C.-S.S.; formal analysis, Y.-C.H. (Yun-Ching Huang); investigation, Y.-L.L.; resources, Y.-C.H. (Yun-Ching Huang); data curation, Y.-L.L. and Y.-C.H. (Yun-Ching Huang); writing—original draft preparation, Y.-L.L.; writing—review and editing, Y.-C.H. (Yun-Ching Huang); supervision, C.-T.W. and C.-S.C.; project administration, Y.-C.H. (Yun-Ching Huang); funding acquisition, Y.-C.H. (Yun-Ching Huang). All authors have read and agreed to the published version of the manuscript.
Funding
The APC was funded by Chang Gung Medical Foundation, Taiwan (BMRPB51).
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board of Chang Gung Memorial Hospital (IRB No. 202100779B0).
Informed Consent Statement
Patient consent was waived due to the retrospective nature of this study.
Data Availability Statement
Data availability is limited due to institutional data protection law and confidentiality of patient data.
Acknowledgments
We would like to thank Chia-Hao Chang for supervision of the statistical analysis and Alan W. Shindel for assistance in manuscript preparation.
Conflicts of Interest
The authors have no conflict of interest to declare.
References
- Lees, J.S.; Elyan, B.M.P.; Herrmann, S.M.; Lang, N.N.; Jones, R.J.; Mark, P.B. The ‘other’ big complication: How chronic kidney disease impacts on cancer risks and outcomes. Nephrol. Dial. Transplant. 2022, 0, 1–9. [Google Scholar] [CrossRef] [PubMed]
- Johansen, K.L.; Chertow, G.M.; Gilbertson, D.T.; Herzog, C.A.; Ishani, A.; Israni, A.K.; Ku, E.; Li, S.; Li, S.; Liu, J.; et al. US Renal Data System 2021 Annual Data Report: Epidemiology of Kidney Disease in the United States. Am. J. Kidney Dis. 2022, 79, A8–A12. [Google Scholar] [CrossRef] [PubMed]
- Wong, G.; Staplin, N.; Emberson, J.; Baigent, C.; Turner, R.; Chalmers, J.; Zoungas, S.; Pollock, C.; Cooper, B.; Harris, D.; et al. Chronic kidney disease and the risk of cancer: An individual patient data meta-analysis of 32,057 participants from six prospective studies. BMC Cancer 2016, 16, 488. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Chang, C.H.; Yang, C.M.; Yang, A.H. Renal diagnosis of chronic hemodialysis patients with urinary tract transitional cell carcinoma in Taiwan. Cancer 2007, 109, 1487–1492. [Google Scholar] [CrossRef] [PubMed]
- Witjes, J.A.; Bruins, H.M.; Cathomas, R.; Comperat, E.M.; Cowan, N.C.; Gakis, G.; Hernandez, V.; Linares Espinos, E.; Lorch, A.; Neuzillet, Y.; et al. European Association of Urology Guidelines on Muscle-invasive and Metastatic Bladder Cancer: Summary of the 2020 Guidelines. Eur. Urol. 2021, 79, 82–104. [Google Scholar] [CrossRef]
- Kellerman, P.S. Perioperative care of the renal patient. Arch. Intern. Med. 1994, 154, 1674–1688. [Google Scholar] [CrossRef]
- Sato, Y.; Kondo, T.; Takagi, T.; Junpei, I.; Tanabe, K. Treatment strategy for bladder cancer in patients on hemodialysis: A clinical review of 28 cases. Int. Urol. Nephrol. 2016, 48, 503–509. [Google Scholar] [CrossRef]
- Shabsigh, A.; Korets, R.; Vora, K.C.; Brooks, C.M.; Cronin, A.M.; Savage, C.; Raj, G.; Bochner, B.H.; Dalbagni, G.; Herr, H.W.; et al. Defining early morbidity of radical cystectomy for patients with bladder cancer using a standardized reporting methodology. Eur. Urol. 2009, 55, 164–174. [Google Scholar] [CrossRef]
- Lee, T.H.; Marcantonio, E.R.; Mangione, C.M.; Thomas, E.J.; Polanczyk, C.A.; Cook, E.F.; Sugarbaker, D.J.; Donaldson, M.C.; Poss, R.; Ho, K.K.; et al. Derivation and prospective validation of a simple index for prediction of cardiac risk of major noncardiac surgery. Circulation 1999, 100, 1043–1049. [Google Scholar] [CrossRef] [Green Version]
- Pinson, C.W.; Schuman, E.S.; Gross, G.F.; Schuman, T.A.; Hayes, J.F. Surgery in long-term dialysis patients. Experience with more than 300 cases. Am. J. Surg. 1986, 151, 567–571. [Google Scholar] [CrossRef]
- Sohal, A.S.; Gangji, A.S.; Crowther, M.A.; Treleaven, D. Uremic bleeding: Pathophysiology and clinical risk factors. Thromb. Res. 2006, 118, 417–422. [Google Scholar] [CrossRef] [PubMed]
- Birkmeyer, J.D.; Stukel, T.A.; Siewers, A.E.; Goodney, P.P.; Wennberg, D.E.; Lucas, F.L. Surgeon volume and operative mortality in the United States. N. Engl. J. Med. 2003, 349, 2117–2127. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Dindo, D.; Demartines, N.; Clavien, P.A. Classification of surgical complications: A new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann. Surg. 2004, 240, 205–213. [Google Scholar] [CrossRef] [PubMed]
- Gakis, G.; Efstathiou, J.; Lerner, S.P.; Cookson, M.S.; Keegan, K.A.; Guru, K.A.; Shipley, W.U.; Heidenreich, A.; Schoenberg, M.P.; Sagaloswky, A.I.; et al. ICUD-EAU International Consultation on Bladder Cancer 2012: Radical cystectomy and bladder preservation for muscle-invasive urothelial carcinoma of the bladder. Eur. Urol. 2013, 63, 45–57. [Google Scholar] [CrossRef] [PubMed]
- Huang, Y.C.; Chang, Y.H.; Shindel, A.W.; Chang, Y.L.; Lin, J.H.; Ho, D.R.; Chen, C.S. Perioperative Complications and Mortality in Patients with Urothelial Carcinoma and End-Stage Renal Disease Undergoing One-Stage Complete Urinary Tract Extirpation. Ann. Surg. Oncol. 2018, 25, 573–581. [Google Scholar] [CrossRef]
- Huang, Y.C.; Chang, Y.H.; Chiu, K.H.; Shindel, A.W.; Lai, C.H. Adjuvant radiotherapy for locally advanced upper tract urothelial carcinoma. Sci. Rep. 2016, 6, 38175. [Google Scholar] [CrossRef] [Green Version]
- Huang, Y.C.; Chen, M.F.; Shi, C.S.; Shindel, A.W.; Huang, C.E.; Pang, S.T.; Chuang, C.K.; Chen, C.S.; Chang, Y.H.; Lin, W.Y.; et al. The Efficacy of Postoperative Adjuvant Chemotherapy for Patients with pT3N0M0 Upper Tract Urothelial Carcinoma. J. Urol. 2015, 194, 323–329. [Google Scholar] [CrossRef]
- Tseng, S.F.; Chuang, Y.C.; Yang, W.C. Long-term outcome of radical cystectomy in ESDR patients with bladder urothelial carcinoma. Int. Urol. Nephrol. 2011, 43, 1067–1071. [Google Scholar] [CrossRef]
- Yossepowitch, O.; Sagy, I.; Margel, D.; Baniel, J. Urothelial carcinoma of the bladder in patients on hemodialysis: Clinical characteristics and oncological outcomes. J. Urol. 2012, 187, 1215–1219. [Google Scholar] [CrossRef]
- Johnson, S.C.; Smith, Z.L.; Golan, S.; Rodriguez, J.F., 3rd; Pearce, S.M.; Smith, N.D.; Steinberg, G.D. Perioperative and long-term outcomes after radical cystectomy in hemodialysis patients. Urol. Oncol. 2018, 36, 237.e19–237.e24. [Google Scholar] [CrossRef]
- Fitz-Henry, J. The ASA classification and peri-operative risk. Ann. R. Coll. Surg. Engl. 2011, 93, 185–187. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Owens, W.D.; Felts, J.A.; Spitznagel, E.L., Jr. ASA physical status classifications: A study of consistency of ratings. Anesthesiology 1978, 49, 239–243. [Google Scholar] [CrossRef] [PubMed]
- Charlson, M.E.; Pompei, P.; Ales, K.L.; MacKenzie, C.R. A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation. J. Chronic. Dis. 1987, 40, 373–383. [Google Scholar] [CrossRef]
- Yuh, B.E.; Nazmy, M.; Ruel, N.H.; Jankowski, J.T.; Menchaca, A.R.; Torrey, R.R.; Linehan, J.A.; Lau, C.S.; Chan, K.G.; Wilson, T.G. Standardized analysis of frequency and severity of complications after robot-assisted radical cystectomy. Eur. Urol. 2012, 62, 806–813. [Google Scholar] [CrossRef]
- Chang, S.S.; Cookson, M.S.; Baumgartner, R.G.; Wells, N.; Smith, J.A., Jr. Analysis of early complications after radical cystectomy: Results of a collaborative care pathway. J. Urol. 2002, 167, 2012–2016. [Google Scholar] [CrossRef]
- Novara, G.; De Marco, V.; Aragona, M.; Boscolo-Berto, R.; Cavalleri, S.; Artibani, W.; Ficarra, V. Complications and mortality after radical cystectomy for bladder transitional cell cancer. J. Urol. 2009, 182, 914–921. [Google Scholar] [CrossRef]
- Hollenbeck, B.K.; Miller, D.C.; Taub, D.; Dunn, R.L.; Khuri, S.F.; Henderson, W.G.; Montie, J.E.; Underwood, W., 3rd; Wei, J.T. Identifying risk factors for potentially avoidable complications following radical cystectomy. J. Urol. 2005, 174, 1231–1237, discussion 1237. [Google Scholar] [CrossRef]
- Bruins, H.M.; Veskimae, E.; Hernandez, V.; Neuzillet, Y.; Cathomas, R.; Comperat, E.M.; Cowan, N.C.; Gakis, G.; Espinos, 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] [CrossRef]
- Satoh, S.; Tsuchiya, N.; Habuchi, T.; Ishiyama, T.; Seimo, K.; Kato, T. Renal cell and transitional cell carcinoma in a Japanese population undergoing maintenance dialysis. J. Urol. 2005, 174, 1749–1753. [Google Scholar] [CrossRef]
- Cheng, T.M. Reflections on the 20th anniversary of Taiwan’s single-payer National Health Insurance System. Health Aff. (Millwood) 2015, 34, 502–510. [Google Scholar] [CrossRef]
- Huang, Y.C.; Liu, Y.L.; Chen, M.F.; Chen, C.S.; Wu, C.T. Treatment Strategy for Dialysis Patient with Urothelial Carcinoma. Diagnostics 2021, 11, 1966. [Google Scholar] [CrossRef] [PubMed]
- Yasin, S.; Holley, J.L. When ESKD complicates cancer screening and cancer treatment. Semin. Dial. 2020, 33, 236–244. [Google Scholar] [CrossRef]
- Anderson, R.T.; Cleek, H.; Pajouhi, A.S.; Bellolio, M.F.; Mayukha, A.; Hart, A.; Hickson, L.J.; Feely, M.A.; Wilson, M.E.; Giddings Connolly, R.M.; et al. Prediction of Risk of Death for Patients Starting Dialysis: A Systematic Review and Meta-Analysis. Clin. J. Am. Soc. Nephrol. 2019, 14, 1213–1227. [Google Scholar] [CrossRef] [PubMed]
- Noh, J.; Yoo, K.D.; Bae, W.; Lee, J.S.; Kim, K.; Cho, J.H.; Lee, H.; Kim, D.K.; Lim, C.S.; Kang, S.W.; et al. Prediction of the Mortality Risk in Peritoneal Dialysis Patients using Machine Learning Models: A Nation-wide Prospective Cohort in Korea. Sci. Rep. 2020, 10, 7470. [Google Scholar] [CrossRef] [PubMed]
- Collaborators, G.B.D.M. Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970-2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet 2017, 390, 1084–1150. [Google Scholar] [CrossRef] [Green Version]
- Lin, Y.C.; Liao, C.T.; Zheng, C.M.; Lin, M.H.; Hsu, C.C.; Hsu, Y.H.; Wu, M.S. Clinical characteristics and outcomes of patients requiring incident dialysis in Taiwan. J. Formos. Med. Assoc. 2022, 121, S56–S63. [Google Scholar] [CrossRef] [PubMed]
- Wu, B.S.; Wei, C.H.; Yang, C.Y.; Lin, M.H.; Hsu, C.C.; Hsu, Y.J.; Lin, S.H.; Tarng, D.C. Mortality rate of end-stage kidney disease patients in Taiwan. J. Formos. Med. Assoc. 2022, 121 (Suppl. 1), S12–S19. [Google Scholar] [CrossRef]
- Chiu, H.F.; Chung, M.C.; Chung, C.J.; Yu, T.M.; Shu, K.H.; Wu, M.J. Prognosis of Kidney Transplant Recipients With Pretransplantation Malignancy: A Nationwide Population-Based Cohort Study in Taiwan. Transplant. Proc. 2016, 48, 918–920. [Google Scholar] [CrossRef]
Table 1.
Clinical characteristics of dialysis patients undergoing radical cystectomy.
| Total (n = 141) | No Major Complication (Clavien 0–2, n = 99) | Major Complication (Clavien 3–5, n = 42) | p Value | |
|---|---|---|---|---|
| Gender | 0.348 | |||
| Female | 84 (59.6) | 56 (56.6) | 28 (66.7) | |
| Male | 57 (40.4) | 43 (43.4) | 14 (33.3) | |
| Age, years, median (range) | 64 (24–86) | 63 (24–86) | 70 (50–83) | 0.010 0.062 |
| <60 | 56 (39.7) | 45 (45.5) | 11 (26.2) | |
| 60–70 | 33 (23.4) | 23 (23.2) | 10 (23.8) | |
| >70 | 52 (36.9) | 31 (31.3) | 21 (50.0) | |
| BMI, kg/m2, median (range) | 23.0 (16.2–38.1) | 22.9 (17.5–38.1) | 23.3 (16.2–32.7) | 0.799 0.684 |
| <25.0 | 98 (69.5) | 70 (70.7) | 28 (66.7) | |
| ≥25.0 | 40 (28.4) | 27 (27.3) | 13 (31.0) | |
| Unknown | 3 (2.1) | 2 (2.0) | 1 (2.4) | |
| CCI, median (range) a | 5 (3–9) | 4 (3–9) | 5 (4–9) | 0.003 0.002 |
| ≤4 | 62 (44.0) | 52 (52.5) | 10 (23.8) | |
| ≥5 | 79 (56.0) | 47 (47.5) | 32 (76.2) | |
| Previous abdominal surgery | 73 (51.8) | 52 (52.5) | 21 (50.0) | 0.855 |
| Renal replacement therapy | 0.984 | |||
| Hemodialysis | 119 (84.4) | 84 (84.8) | 35 (83.3) | |
| Peritoneal dialysis | 15 (10.6) | 10 (10.1) | 5 (11.9) | |
| Kidney transplantation | 4 (2.8) | 3 (3.0) | 1 (2.4) | |
| None | 3 (2.1) | 2 (2.0) | 1 (2.4) | |
| Dialysis duration, years | 0.646 | |||
| <5 | 67 (47.5) | 45 (45.5) | 22 (52.4) | |
| 5–10 | 41 (29.1) | 31 (31.3) | 10 (23.8) | |
| >10 | 33 (23.4) | 23 (23.2) | 10 (23.8) | |
| Hemoglobin, g/dL, median (range) a | 10.1 (6.0–15.7) | 10.1 (6.8–15.7) | 10.2 (6.0–12.7) | 0.540 1.000 |
| ≤10.1 | 72 (51.1) | 51 (51.5) | 21 (50.0) | |
| >10.1 | 69 (48.9) | 48 (48.5) | 21 (50.0) | |
| Potassium, mEq/L, median (range) b | 4.2 (2.7–6.8) | 4.2 (2.7–6.8) | 4.3 (3.3–5.7) | 0.815 0.090 |
| <3.6 | 13 (9.2) | 12 (12.1) | 1 (2.4) | |
| 3.6–5.0 | 86 (61.0) | 56 (56.6) | 30 (71.4) | |
| >5.0 | 19 (13.5) | 15 (15.2) | 4 (9.5) | |
| Unknown | 23 (16.3) | 16 (16.2) | 7 (16.7) | |
| Cystectomy year | 0.547 | |||
| 2004–2007 | 47 (33.3) | 34 (34.3) | 13 (31.0) | |
| 2008–2011 | 43 (30.5) | 32 (32.3) | 11 (26.2) | |
| 2012–2015 | 51 (36.2) | 33 (33.3) | 18 (42.9) | |
| ASA score, median (range) | 3 (1–4) | 3 (1–3) | 3 (2–4) | 0.235 0.387 |
| 1 | 1 (0.7) | 1 (1.0) | 0 (0) | |
| 2 | 9 (6.4) | 7 (7.1) | 2 (4.8) | |
| 3 | 130 (92.2) | 91 (91.9) | 39 (92.9) | |
| 4 | 1 (0.7) | 0 (0) | 1 (2.4) | |
| Surgeon volume, median (range) | 3 (1–27) | 0.003 | ||
| Low, <9 cases | 62 (44.0) | 35 (35.4) | 27 (64.3) | |
| High, ≥9 cases | 79 (56.0) | 64 (64.6) | 15 (35.7) | |
| Operative methods | 0.839 | |||
| Open | 101 (71.6) | 70 (70.7) | 31 (73.8) | |
| Laparoscopic | 40 (28.4) | 29 (29.3) | 11 (26.2) | |
| Operative time, min, median (range) a | 343 (68–676) | 337 (68–660) | 351 (213–676) | 0.280 0.715 |
| ≤343 | 71 (50.4) | 51 (51.5) | 20 (47.6) | |
| >343 | 70 (49.6) | 48 (48.5) | 22 (52.4) | |
| Blood loss, mL, median (range) a | 600 (50–8600) | 600 (50–6000) | 600 (100–8600) | 0.237 1.000 |
| <600 | 68 (48.2) | 48 (48.5) | 20 (47.6) | |
| ≥600 | 72 (51.1) | 50 (50.5) | 22 (52.4) | |
| Unknown | 1 (0.7) | 1 (1.0) | 0 (0) | |
| Hospitalization, day, median (range) | 9 (2–145) | 9 (4–52) | 14 (2–145) | <0.001 |
Data are expressed as n (%) unless otherwise specified. Significant p-values are shown in bold. a The cutoff values of the variables were determined according to median values in the study cohort. b Reference range of plasma potassium was 3.6–5.0 mEq/L. BMI: body mass index; CCI: Charlson comorbidity index; ASA: American Society of Anesthesiologists.
Table 2.
Pathological features of dialysis patients undergoing radical cystectomy.
| Total (n = 141) | No Major Complication (Clavien 0–2, n = 99) | Major Complication (Clavien 3–5, n = 42) | p Value | |
|---|---|---|---|---|
| Pathological tumor stage | 0.372 | |||
| 0a/0is | 26 (18.4) | 18 (18.2) | 8 (19.0) | |
| I | 37 (26.2) | 27 (27.3) | 10 (23.8) | |
| II | 13 (9.2) | 8 (8.1) | 5 (11.9) | |
| III | 9 (6.4) | 4 (4.0) | 5 (11.9) | |
| IV | 4 (2.8) | 2 (2.0) | 2 (4.8) | |
| No residual tumor | 52 (36.9) | 40 (40.4) | 12 (28.6) | |
| Tumor grade a | 1.000 | |||
| Low | 5 (5.6) | 3 (5.1) | 2 (6.7) | |
| High | 84 (94.4) | 56 (94.9) | 28 (93.3) | |
| Lymphovascular invasion | 0.065 | |||
| Absent | 131 (92.9) | 95 (96.0) | 36 (85.7) | |
| Present | 10 (7.1) | 4 (4.0) | 6 (14.3) | |
| Surgical margin | 1.000 | |||
| Negative | 136 (96.5) | 95 (96.0) | 41 (97.6) | |
| Positive | 5 (3.5) | 4 (4.0) | 1 (2.4) | |
| Concomitant carcinoma in situ | 0.755 | |||
| Absent | 128 (90.8) | 89 (89.9) | 39 (92.9) | |
| Present | 13 (9.2) | 10 (10.1) | 3 (7.1) |
Data are expressed as n (%). The pathologic features were determined according to the time of radical cystectomy. a Fifty-two patients with no residual tumor in the radical cystectomy procedure were excluded.
Table 3.
Complication grade and type after radical cystectomy (n = 141).
| Grade 0 | 25 (17.7) |
| Grade 1 | 25 (17.7) |
| Grade 2 | 49 (34.8) |
| Pharmacological treatment other than grade 1 | 25 (17.7) |
| Blood transfusion | 18 (12.8) |
| Total parenteral nutrition | 6 (4.3) |
| Grade 3 | 29 (20.6) |
| Surgical intervention | 24 (17.0) |
| arteriovenous shunt dysfunction | 10 (7.1) |
| rectovaginal or vaginal fistula | 3 (2.1) |
| infection | 3 (2.1) |
| wound dehiscence | 2 (1.4) |
| spleen laceration or splenectomy | 2 (1.4) |
| bowel perforation | 2 (1.4) |
| vaginal bleeding | 1 (0.7) |
| ischemic leg | 1 (0.7) |
| Radiological intervention | 4 (2.8) |
| Endoscopic intervention | 1 (0.7) |
| Grade 4 | 6 (4.3) |
| Life-threatening single organ dysfunction | 5 (3.5) |
| Life-threatening multiorgan dysfunction | 1 (0.7) |
| Grade 5, death | 7 (5.0) |
Data are expressed as n (%). Complications were graded according to the Clavien classification of surgical complications.
Table 4.
Univariate and multivariate analysis for predictive factors of postoperative major complications.
Table 4.
Univariate and multivariate analysis for predictive factors of postoperative major complications.
| Univariate | Multivariate | |||
|---|---|---|---|---|
| OR (95% CI) | p Value | OR (95% CI) | p Value | |
| Male gender (referent: female) | 0.65 (0.31–1.39) | 0.265 | ||
| Age (referent: < 60 years) | 0.068 | 0.213 | ||
| 60–70 | 1.78 (0.66–4.80) | 0.256 | 1.72 (0.58–5.12) | 0.332 |
| >70 | 2.77 (1.17–6.56) | 0.020 | 2.31 (0.91–5.90) | 0.079 |
| BMI ≥ 25 kg/m2 (referent: <25 kg/m2) | 1.20 (0.54–2.66) | 0.647 | ||
| CCI ≥ 5 (referent: ≤4) a | 3.54 (1.57–7.98) | 0.002 | 3.43 (1.43–8.23) | 0.006 |
| Previous abdominal surgery (referent: absent) | 0.90 (0.44–1.86) | 0.784 | ||
| RRT (referent: hemodialysis) | 0.932 | |||
| Kidney transplantation | 0.80 (0.08–7.96) | 0.849 | ||
| Peritoneal dialysis | 1.20 (0.38–3.77) | 0.755 | ||
| Dialysis duration (referent: <5 years) | 0.648 | |||
| 5–10 years | 0.66 (0.28–1.59) | 0.352 | ||
| >10 years | 0.88 (0.36–2.19) | 0.799 | ||
| Hemoglobin ≤ 10.1 g/dL (referent: >10.1 g/dL) a | 0.94 (0.46–1.94) | 0.869 | ||
| Potassium (referent: 3.6–5.0 mEq/L) b | 0.130 | |||
| <3.6 | 0.16 (0.02–1.26) | 0.081 | ||
| >5.0 | 0.50 (0.15–1.63) | 0.250 | ||
| Cystectomy year (referent: 2004–2007) | 0.549 | |||
| 2008–2011 | 0.90 (0.35–2.29) | 0.824 | ||
| 2012–2015 | 1.43 (0.60–3.37) | 0.418 | ||
| ASA score ≥ 3 (referent: ASA ≤ 2) | 1.76 (0.36–8.65) | 0.488 | ||
| Low-volume surgeon (referent: ≥ 9 cases) c | 3.29 (1.55–6.99) | 0.002 | 3.29 (1.46–7.40) | 0.004 |
| Open method (referent: laparoscopy) | 1.17 (0.52–2.63) | 0.709 | ||
| Operative time > 343 min (referent: ≤ 343 min) a | 1.17 (0.57–2.41) | 0.672 | ||
| Blood loss ≥ 600 mL (referent: <600 mL) a | 1.06 (0.51–2.18) | 0.883 | ||
| Stage 3/4 (referent: stage ≤ 2) | 3.10 (0.97–9.87) | 0.055 | ||
| Tumor grade (referent: low grade) | 0.75 (0.12–4.75) | 0.760 | ||
| Lymphovascular invasion (referent: absent) | 3.96 (1.06–14.8) | 0.041 | 3.46 (0.81–14.8) | 0.094 |
| Surgical margin (referent: negative) | 0.58 (0.06–5.34) | 0.630 | ||
| CIS (referent: absent) | 0.69 (0.18–2.63) | 0.581 | ||
Significant p-values are shown in bold. a The cutoff values of the variables were determined according to median values in the study cohort. b Reference range of plasma potassium was 3.6–5.0 mEq/L. c Low-volume surgeons classified as those performing fewer than 9 cases during the study. OR: odds ratio; CI: confidence interval; BMI: body mass index; CCI: Charlson comorbidity index; RRT: renal replacement therapy; ASA: American Society of Anesthesiologists; CIS: concomitant carcinoma in situ.
Table 5.
Univariate and multivariate analysis of potential prognostic factors for overall, cancer-specific, and recurrence-free survival in dialysis patients undergoing radical cystectomy.
Table 5.
Univariate and multivariate analysis of potential prognostic factors for overall, cancer-specific, and recurrence-free survival in dialysis patients undergoing radical cystectomy.
| Overall Survival | Cancer-Specific Survival | Recurrence-Free Survival | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Univariate | Multivariate | Univariate | Multivariate | Univariate | Multivariate | |||||||
| HR (95% CI) | p Value | HR (95% CI) | p Value | HR (95% CI) | p Value | HR (95% CI) | p Value | HR (95% CI) | p Value | HR (95% CI) | p Value | |
| Male gender (referent: female) | 2.09 (1.10–3.95) | 0.024 | 2.36 (1.15–4.83) | 0.019 | 2.49 (0.56–11.1) | 0.233 | 1.95 (0.71–5.38) | 0.198 | ||||
| Age (referent: <60 years) | <0.001 | 0.023 | 0.965 | 0.299 | ||||||||
| 60–70 years | 1.60 (0.57–4.46) | 0.372 | 1.27 (0.44–3.65) | 0.659 | 0 (0–1000) | 0.971 | 0.26 (0.03–2.13) | 0.210 | ||||
| >70 years | 4.48 (2.06–9.74) | <0.001 | 2.91 (1.29–6.60) | 0.010 | 1.22 (0.27–5.50) | 0.792 | 1.36 (0.48–3.90) | 0.564 | ||||
| BMI ≥ 25 kg/m2 (referent: <25 kg/m2) | 0.68 (0.31–1.49) | 0.338 | 0.40 (0.05–3.32) | 0.396 | 0.83 (0.26–2.60) | 0.744 | ||||||
| CCI ≥ 5 (referent: ≤4) a | 4.30 (1.89–9.79) | 0.001 | 4.03 (1.54–10.5) | 0.004 | 2.26 (0.44–11.7) | 0.329 | 2.35 (0.75–7.39) | 0.143 | ||||
| Previous abdominal surgery (referent: absent) | 0.80 (0.42–1.51) | 0.484 | 2.23 (0.43–11.5) | 0.339 | 1.29 (0.46–3.62) | 0.633 | ||||||
| RRT (referent: hemodialysis) | 0.438 | 0.214 | 0.039 | 0.102 | ||||||||
| Kidney transplantation | 2.10 (0.50–8.79) | 0.311 | 6.80 (0.79–58.3) | 0.080 | 7.19 (1.57–32.8) | 0.011 | 6.75 (1.09–41.7) | 0.040 | ||||
| Peritoneal dialysis | 0.65 (0.20–2.12) | 0.473 | 1.64 (0.19–14.1) | 0.650 | 1.49 (0.33–6.80) | 0.609 | 0.97 (0.16–5.97) | 0.972 | ||||
| Dialysis duration (referent: <5 years) | 0.356 | 0.713 | 0.597 | |||||||||
| 5–10 years | 0.72 (0.34–1.52) | 0.385 | 1.39 (0.28–6.90) | 0.685 | 0.93 (0.31–2.85) | 0.902 | ||||||
| >10 years | 0.56 (0.24–1.31) | 0.179 | 0.55 (0.06–5.25) | 0.599 | 0.45 (0.10–2.13) | 0.316 | ||||||
| Hemoglobin ≤ 10.1 g/dL (referent: >10.1 g/dL) a | 0.86 (0.45–1.63) | 0.638 | 1.33 (0.30–5.94) | 0.709 | 1.49 (0.53–4.19) | 0.450 | ||||||
| Potassium (referent: 3.6–5.0 mEq/L) b | 0.906 | 0.684 | 0.978 | |||||||||
| <3.6 | 1.18 (0.41–3.45) | 0.758 | 0.989 | 0.981 | ||||||||
| >5.0 | 0.86 (0.30–2.52) | 0.789 | 2.13 (0.39–11.6) | 0.383 | 0.85 (0.19–3.84) | 0.834 | ||||||
| Cystectomy year (referent: 2004–2007) | 0.909 | 0.496 | 0.846 | |||||||||
| 2008–2011 | 1.12 (0.53–2.38) | 0.765 | 3.56 (0.37–34.2) | 0.272 | 0.89 (0.24–3.32) | 0.862 | ||||||
| 2012–2015 | 1.20 (0.51–2.81) | 0.676 | 3.64 (0.38–35.1) | 0.265 | 1.27 (0.39–4.21) | 0.693 | ||||||
| ASA score ≥ 3 (referent: ASA ≤ 2) | 0.68 (0.27–1.76) | 0.431 | 0.23 (0.04–1.18) | 0.077 | 0.54 (0.12–2.40) | 0.419 | ||||||
| Low surgeon volume (referent: ≥9 cases) c | 1.96 (1.03–3.75) | 0.042 | 1.26 (0.58–2.71) | 0.562 | 1.91 (0.43–8.55) | 0.397 | 2.22 (0.79–6.23) | 0.132 | ||||
| Open method (referent: laparoscopic) | 1.60 (0.73–3.49) | 0.237 | 2.66 (0.32–22.1) | 0.366 | 1.73 (0.49–6.12) | 0.399 | ||||||
| Operative time > 343 min (referent: ≤343 min) a | 0.79 (0.42–1.51) | 0.480 | 0.15 (0.02–1.25) | 0.080 | 1.13 (0.41–3.11) | 0.817 | ||||||
| Blood loss ≥ 600 mL (referent: <600 mL) a | 1.73 (0.90–3.35) | 0.103 | 2.44 (0.47–12.6) | 0.288 | 2.78 (0.88–8.72) | 0.080 | ||||||
| Stage 3/4 (referent: stage ≤ 2) | 5.54 (2.37–12.9) | <0.001 | 37.2 (6.44–215) | <0.001 | 9.12 (1.73–48.0) | 0.009 | 6.61 (1.04–42.1) | 0.046 | 20.0 (7.00–56.9) | <0.001 | 3.78 (0.51–28.2) | 0.196 |
| Tumor grade (referent: low grade) | 0.62 (0.34–1.13) | 0.117 | 0.37 (0.04–3.07) | 0.357 | 0.26 (0.06–1.16) | 0.077 | ||||||
| Lymphovascular invasion (referent: absent) | 4.17 (1.60–10.9) | 0.004 | 0.10 (0.01–0.76) | 0.026 | 4.18 (0.50–35.2) | 0.188 | 20.6 (7.12–59.6) | <0.001 | 4.42 (0.50–38.7) | 0.180 | ||
| Surgical margin (referent: negative) | 8.06 (2.30–28.2) | 0.001 | 1.97 (0.37–10.5) | 0.425 | 19.2 (1.85–200) | 0.013 | 8.90 (0.61–128) | 0.109 | 21.0 (6.20–71.4) | <0.001 | 4.59 (0.65–32.6) | 0.128 |
| CIS (referent: absent) | 0.73 (0.22–2.38) | 0.603 | 1.40 (0.17–11.6) | 0.758 | 0.66 (0.09–5.02) | 0.687 | ||||||
| Clavien grade 3–5 (referent: 0–2) | 3.43 (1.80–6.53) | <0.001 | 3.58 (1.61–7.95) | 0.002 | 0.44 (0.05–3.64) | 0.444 | 1.49 (0.51–4.36) | 0.469 | ||||
Significant p-values are shown in bold. a The cutoff values of the variables were determined according to median values in the study cohort. b Reference range of random plasma potassium was 3.6–5.0 mEq/L. c Low-volume surgeons classified as those performing fewer than 9 cases during the study. HR: hazard ratio; CI: confidence interval; BMI: body mass index; CCI: Charlson comorbidity index; RRT: renal replacement therapy; ASA: American Society of Anesthesiologists.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Liu, Y.-L.; Wu, C.-T.; Hsu, Y.-C.; Chen, M.-F.; Chen, C.-S.; Shi, C.-S.; Huang, Y.-C. Perioperative Complications and Oncologic Outcomes after Radical Cystectomy in End-Stage Renal Disease Patients with Bladder Cancer Obtained Using a Standardized Reporting System. Cancers 2022, 14, 3512. https://doi.org/10.3390/cancers14143512
AMA Style
Liu Y-L, Wu C-T, Hsu Y-C, Chen M-F, Chen C-S, Shi C-S, Huang Y-C. Perioperative Complications and Oncologic Outcomes after Radical Cystectomy in End-Stage Renal Disease Patients with Bladder Cancer Obtained Using a Standardized Reporting System. Cancers. 2022; 14(14):3512. https://doi.org/10.3390/cancers14143512
Chicago/Turabian StyleLiu, Yu-Liang, Chun-Te Wu, Yu-Chao Hsu, Miao-Fen Chen, Chih-Shou Chen, Chung-Sheng Shi, and Yun-Ching Huang. 2022. "Perioperative Complications and Oncologic Outcomes after Radical Cystectomy in End-Stage Renal Disease Patients with Bladder Cancer Obtained Using a Standardized Reporting System" Cancers 14, no. 14: 3512. https://doi.org/10.3390/cancers14143512
APA StyleLiu, Y.-L., Wu, C.-T., Hsu, Y.-C., Chen, M.-F., Chen, C.-S., Shi, C.-S., & Huang, Y.-C. (2022). Perioperative Complications and Oncologic Outcomes after Radical Cystectomy in End-Stage Renal Disease Patients with Bladder Cancer Obtained Using a Standardized Reporting System. Cancers, 14(14), 3512. https://doi.org/10.3390/cancers14143512
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
