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Research Papers:

Patients with urothelial carcinoma have poor renal outcome regardless of whether they receive nephrouretectomy

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Oncotarget. 2016; 7:61679-61689. https://doi.org/10.18632/oncotarget.11223

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Peir-Haur Hung, Hung-Bin Tsai, Kuan-Yu Hung, Chih-Hsin Muo, Mu-Chi Chung, Chao-Hsiang Chang and Chi-Jung Chung _

Abstract

Peir-Haur Hung1,2, Hung-Bin Tsai3, Kuan-Yu Hung4, Chih-Hsin Muo5, Mu-Chi Chung6, Chao-Hsiang Chang7, Chi-Jung Chung8,9

1Department of Internal Medicine, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan

2Department of Applied Life Science and Health, Chia-Nan University of Pharmacy and Science, Tainan, Taiwan

3Department of Tramatology, National Taiwan University Hospital, Taipei, Taiwan

4Department of Internal Medicine, National Taiwan University Hospital, Hsin-Chu Branch, Hsin-Chu City, Taiwan

5Management Office for Health Data, China Medical University and Hospital, Taichung, Taiwan

6Division of Nephrology, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

7Department of Urology, China Medical University and Hospital, Taichung, Taiwan

8Department of Health Risk Management, College of Public Health, China Medical University, Taichung, Taiwan

9Department of Medical Research, China Medical University Hospital, Taichung, Taiwan

Correspondence to:

Chi-Jung Chung, email: [email protected]

Keywords: chronic kidney disease, end stage renal disease, nephrouretectomy, urothelial carcinoma

Received: March 04, 2016    Accepted: July 27, 2016    Published: August 11, 2016

ABSTRACT

The association between urothelial carcinoma (UC) and subsequent ESRD incidence has not been confirmed. This was a population-based study using claims data from the Taiwan National Health Institutes from 1998 to 2010. The study cohort consisted of 26,017 patients with newly diagnosed UC and no history of ESRD, and the comparison cohort consisted of 208,136 matched enrollees without UC. The incidence of ESRD was ascertained through cross-referencing with a registry for catastrophic illnesses. Cox proportional hazard regression analysis was used to estimate the risk of ESRD associated with UC and UC subtype. A total of 979 patients (3.76%) from the UC group and 1,829 (0.88%) from the comparison group developed ESRD. Multivariable analysis indicated that compared with the comparison group, the hazard ratios (HRs) for ESRD were 7.75 (95% confidence interval [CI]: 6.84 to 8.78) and 3.12 (95% CI: 6.84 to 8.78) in the cohort with upper urinary tract UC (UT-UC) and bladder UC (B-UC), respectively. In addition, there were significantly increased risks for ESRD in UC patients receiving and not receiving nephrouretectomies or aristolochic acids (AA). Moreover, the UC patients receiving segmental ureterectomy and ureteral reimplantation had approximately 1.3-fold and 2.4-fold increased risk for ESRD after control for confounders, respectively. Thus, our data indicate that UT-UC and B-UC independently increased the risk for ESRD in patients after considering about nephrouretectomies or aristolochic acids (AA). In addition, UC patients receiving segmental ureterectomy and ureteral reimplantation had increased risk for ESRD.


INTRODUCTION

End-stage renal disease (ESRD) is a significant public health issue in Taiwan and internationally because patients require significant healthcare services and suffer from reduced quality of life. Taiwan has had the greatest incidence and the second greatest prevalence of ESRD since 2000 in an international comparison based on data from the United States Renal Data System Annual Data Report [1]. Moreover, during the past 10 years, Taiwan has also confronted a serious challenge because the incidence and prevalence of ESRD have increased 2.6 and 3.7 times, respectively [2]. Substantial epidemiological and clinical evidence indicates links between hypertension, diabetes, obesity, and metabolic syndrome with the onset and/or progression of chronic kidney disease (CKD) [3], although the effect of urinary tract malignancy on CKD is uncertain.

In Taiwan, urothelial carcinoma (UC) is common among patients with CKD and ESRD [4]. Some research suggests that patients with CKD or ESRD have a greater risk for cancer [5, 6]. In particular, the standardized incidence ratio of UC for patients receiving maintenance dialysis was 48.2 compared with the general population [7]. Furthermore, different dialysis modalities and gender may modify the risk for cancer in patients with ESRD [8]. Meanwhile, UC itself may promote the development of ESRD, especially in patients with upper urinary tract-UC (UT-UC) [9]. However, to date, only limited studies have analyzed the effect of UC on the morbidity and mortality of patients with ESRD [4, 9-11].

Thus, we need more evidence to determine the relationship between UC and development and progression of ESRD. In addition, limited research has evaluated the correlation between the location (or subtype) of UC and the incidence of subsequent ESRD. We propose that patients with UC may face greater risk of ESRD and that different UC subtypes are associated with different risks. We used the nationally representative database of the universal insurance program of Taiwan to determine the association between UC and ESRD.

RESULTS

Baseline characteristics of study subjects

Table 1 shows the sociodemographic characteristics and comorbidities of the comparison cohort, UC cohort, and cohorts with different UC subtypes. The age and sex of comparison and UC cohort were similar because of matching. There were significant differences in the duration from UC to ESRD between comparison and UC cohort, with the UT-UC cohort having the shortest duration (2.9 years) and the comparison cohort having the longest duration (4.8 years). Comparison of comorbidities in the UC and comparison cohorts indicated that the UC cohort had greater prevalences of hypertension, diabetes, coronary heart disease, atrial fibrillation, heart failure, CKD, and hyperlipidemia (p < 0.01 for all comparisons). Comparison of the B-UC and UT-UC cohorts indicated that the UT-UC cohort had higher prevalences of nephrouretectomy and solitary kidney.

Table 1: Demographic characteristics and comorbidities of the control, UC, UT-UC, and B-UC cohorts. Except for follow-up years, numbers indicate N (percent)

Comparison Group

UC

p a

UT-UC

B-UC

Total number

208136

26017

4263

21537

Follow-up years (mean ± SD)

4.79 ± 3.43

3.80 ± 3.27

<0.0001

2.94 ± 2.81

3.98 ± 3.33

Age, years

1.0000

 25–44

9496 (4.56)

1187 (4.56)

130 (3.05)

1036 (4.81)

 45–54

23688 (11.4)

2961 (11.4)

396 (9.29)

2537 (11.8)

 55–64

40504 (19.5)

5063 (19.5)

878 (20.6)

4151 (19.3)

 65–74

66096 (31.8)

8262 (31.8)

1596 (37.4)

6591 (30.6)

 ≥ 75

68352 (32.8)

8544 (32.8)

1263 (29.6)

7222 (33.5)

 Mean (SD)

67.5 ± 12.6

68.2 ± 12.4

68.4 ± 11.0

68.2 ± 12.6

Sex

1.0000

 Male

145176 (69.7)

18147 (69.7)

1857 (43.6)

16176 (75.1)

 Female

62960 (30.3)

7870 (30.3)

2406 (56.4)

5361 (24.9)

Geographic region

<0.0001

 Northern

86554 (41.6)

8970 (34.5)

861 (20.2)

8047 (37.4)

 Central

42928 (20.6)

4888 (18.8)

819 (19.2)

4039 (18.8)

 Southern

57490 (27.6)

9601 (36.9)

2139 (50.2)

7360 (34.2)

 Eastern

21159 (10.2)

2558 (9.83)

444 (10.4)

2091 (9.71)

Occupation

<0.0001

 White collar

88544 (42.6)

11240 (43.2)

1757 (41.2)

9396 (43.6)

 Blue collar

86942 (41.9)

11563 (44.5)

2224 (52.2)

9232 (42.9)

 Others

32237 (15.5)

3208 (12.3)

281 (6.59)

2904 (13.5)

Monthly income, NTD

<0.0001

 ≤ 15840

118082 (56.7)

14832 (57.0)

2149 (50.4)

12569 (58.4)

 15841–20100

9569 (4.60)

2116 (8.13)

387 (9.08)

1700 (7.89)

 > 20100

80485 (38.7)

9069 (34.9)

1727 (40.5)

7268 (33.8)

Comorbidities

 Diabetes

18522 (8.90)

4493 (17.3)

<0.0001

900 (21.1)

3557 (16.5)

 Hypertension

36179 (17.4)

8635 (33.2)

<0.0001

1753 (41.1)

6808 (31.6)

 Coronary heart disease

18544 (8.91)

2988 (11.5)

<0.0001

546 (12.8)

2416 (11.2)

 Atrial fibrillation

3796 (1.82)

537 (2.06)

0.0067

83 (1.95)

452 (2.10)

 Heart failure

5854 (2.81)

880 (3.38)

<0.0001

168 (3.94)

702 (3.26)

 Chronic kidney disease

1266 (0.61)

560 (2.16)

<0.0001

157 (3.68)

400 (1.86)

 Hyperlipidemia

8119 (3.90)

1371 (5.27)

<0.0001

280 (6.57)

1077 (5.00)

 Nephrouretectomy

405 (0.19)

4854 (18.7)

<0.0001

3306 (77.6)

1508 (7.00)

 Solitary kidney

15 (0.01)

58 (0.22)

<0.0001

23 (0.54)

35 (0.16)

B-UC: bladder-urothelial carcinoma, NTD: New Taiwan dollar, SD: standard deviation, UC: urothelial carcinoma, UT-UC: upper urinary tract-urothelial carcinoma.

a P values were evaluated by chi-square test between UC patients and comparison group.

Incidence and hazard ratios of ESRD in the different cohorts

The UC, UT-UC, and B-UC groups had significantly higher ESRD cumulative incidence rates than the comparison group, and these patterns were similar for men and women (Figure 1, p < 0.0001 for all comparisons). In addition, women and men in the UC and B-UC cohorts had similar 3- to 6-fold increased risk for ESRD after adjusting for possible confounding factors (data not shown). Men and women in the UT-UC cohort had the greatest risk for ESRD. Overall, women had a greater risk of ESRD than men, whether in the UC, UT-UC, or B-UC cohort. Moreover, UC patients who received and did not receive nephrouretectomies had increased risks for ESRD, although the hazard ratios (HRs) were greater for those who received nephrouretectomies (Table 2). Except the analysis of stratification, we further added the factor of nephrouretectomies in the models. The significant results for increased risk of ESRD still observed. In addition, we explore the medicine use of aristolochic acids (AA) by above analyzed methods, and found the similar results for increased risk of ESRD.

Cumulative incidence of ESRD in the control cohort and the UC cohort (A. men, B. women), the UT-UC cohort (C. men, D. women), and the B-UC cohort (E. men, F. women).

Figure 1: Cumulative incidence of ESRD in the control cohort and the UC cohort (A. men, B. women), the UT-UC cohort (C. men, D. women), and the B-UC cohort (E. men, F. women).

Table 2: Multivariate Cox proportional hazard models for prediction of ESRD in different cohorts of patients who received and did not receive nephrouretectomies or AA

N of subjects

N of ESRD

Person-years

Rate1

Age, sex-adjusted HR (95% CI)

Model 1a

Model 2

All

Comparison Group

208136

1829

997339

1.83

1.00

1.00

1.00

UC (Total)

26017

979

98929

9.90

5.46 (5.05–5.91)***

3.87 (3.57–4.19)***

 Without Nephrouretectomy

21163

553

82887

6.67

3.72 (3.38-4.09)***

2.74 (2.48-3.01)***

2.76b (2.51-3.04)***

 With Nephrouretectomy

4854

426

16042

26.56

13.8 (12.4-15.4)***

8.88 (7.95-9.93)***

 Without AA

21694

771

82188

9.38

5.19 (4.77-5.64)***

3.69 (3.38-4.02)***

3.18c (2.92-3.46)***

 With AA

4323

208

16740

12.43

6.78 (5.87-7.82)***

4.73 (4.09-5.46)***

UT-UC

4263

330

12515

16.37

13.5 (11.9–15.2)***

7.75 (6.84–8.78)***

 Without Nephrouretectomy

957

73

2221

32.87

16.6 (13.1-21.0)***

7.07 (5.55-9.01)***

3.20b (2.65-3.86)***

 With Nephrouretectomy

3306

257

10294

24.97

13.0 (11.4-14.8)***

8.25 (7.20-9.45)***

 Without AA

3326

250

9741

25.66

13.1 (11.5-15.0)***

7.75 (6.75-8.89)***

6.06c (5.32-6.91)***

With AA

937

80

2774

28.84

14.6 (11.7-18.4)***

7.80 (6.20-9.82)***

B-UC

21537

642

85750

7.49

4.18 (3.82–4.57)***

3.12 (2.84–3.42)***

 Without Nephrouretectomy

20029

475

80137

5.93

3.31 (2.99-3.66)***

2.50 (2.26-2.77)***

2.72b (2.47-3.00)***

 With Nephrouretectomy

1508

167

5613

29.75

15.9 (13.6-18.6)***

10.6 (8.99-12.4)***

 Without AA

18184

516

71919

7.17

4.00 (3.62-4.41)***

2.97 (2.69-3.28)***

2.63c (2.39-2.90)***

 With AA

3353

126

13831

9.11

5.11 (4.26-6.12)***

3.89 (3.24-4.66)***

1Rate per 1000 person-years

ESRD: end-stage renal disease, HR: hazard ratio.

a Multivariate model adjusted for age, sex, geographic region, occupation, monthly income, and comorbidities (diabetes, hypertension, coronary heart disease, atrial fibrillation, heart failure, chronic kidney disease, and hyperlipidemia).

b Add adjusted for nephrouretectomy in model 1.

c Add adjusted for AA in model 1.

Association between clinical management of UC and ESRD

Among all UC patients, 8.2% received segmental ureterectomy and 26% received ureteral reimplantation (Table 3). These groups had approximately 1.3-fold (segmental ureterectomy) and 2.4-fold (ureteral reimplantation) greater risk for ESRD after control for confounding. Among UC patients, 13.7% used cisplatin and 6.1% used carboplatin, and these patients had reduced risk for ESRD; cisplatin (but not carboplatin) also had a protective effect in patients with B-UC. For UT-UC patients, those who received radical cystectomies had a 5.5-fold increased risk for ESRD compared to those who did not receive this surgery.

Table 3: Multivariate Cox proportional hazards model for the prediction of ESRD in all UC patients who received different clinical treatments (Yes vs. No)

UC N (%)

Multivariate-HRs (95% CI)a

UT-UC N (%)

Multivariate-HRs (95% CI)a

B-UC N (%)

Multivariate-HRs (95% CI)a

Endoscopic treatment of bladder

20393 (73.4)

0.94 (0.81-1.10)

1238 (29.0)

1.00 (0.79-1.27)

19105 (88.7)

0.87 (0.67-1.13)

Radical Cystectomy

2528 (9.72)

1.17 (0.77-1.77)

69 (1.62)

4.86 (2.30-10.3)***

2442 (11.3)

0.86 (0.53-1.39)

Segmental ureterectomy

2139 (8.22)

1.29 (1.08-1.55)**

1385 (32.5)

1.06 (0.83-1.36)

742 (3.45)

1.58 (1.19-2.09)**

Endoscopic treatment of ureter

337 (1.30)

1.23 (0.81-1.86)

161 (3.78)

1.23 (0.70-2.17)

176 (0.82)

0.93 (0.50-1.76)

Ureteral reimplantation

6753 (26.0)

2.32 (2.01-2.67)***

2331 (54.7)

1.99 (1.52-2.59)***

4380 (20.3)

2.32 (1.96-2.74)***

Diversion

 Conduits

96 (0.37)

1.22 (0.45-3.29)

9 (0.21)

NA

87 (0.40)

1.93 (0.70-5.31)

 Continent Cutaneous Diversions

676 (2.60)

0.90 (0.50-1.59)

27 (0.63)

0.28 (0.06-1.34)

645 (2.99)

1.07 (0.58-1.99)

 Orthotopic Neobladders

1370 (5.27)

0.84 (0.52-1.38)

21 (0.49)

NA

1340 (6.22)

1.12 (0.65-1.93)

 Nephrouretectomy

4854 (18.7)

1.91 (1.59-2.28)***

3306 (77.6)

0.97 (0.72-1.29)

1508 (7.00)

2.26 (1.76-2.90)***

a Multivariate model adjusted for age, sex, geographic region, occupation, monthly income, and comorbidities (diabetes, hypertension, coronary heart disease, atrial fibrillation, heart failure, chronic kidney disease, and hyperlipidemia).

NA: UT-UCC patients receiving conduits or orthotopic neobladders had no ESRD incidence.

Joint effect of comorbidities and UC on ESRD risk

Comparisons of the UC and comparison cohorts and of the different UC subtypes with the control cohort indicated that patients with CKD, diabetes, and hypertension had significantly increased risk for ESRD (data not shown). Therefore, we calculated the multivariate-adjusted HRs for a combination of comorbidities with UC on the risk for ESRD (Table 4). The results show that UC patients with CKD had the greatest risk for ESRD in all comparisons (Table 4). There were significant joint effects of CKD with UT-UC (interaction p value = 0.0003). In addition, there were also significant joint effects of diabetes and hypertension with UC, with similar results for the UT-UC and B-UC cohorts (data not shown).

Table 4: Interaction between CKD, UC, and UC subtype type on the risk for ESRD

Number, CSS/CN

Multivariate HR (95% CI)a

Trend p values

CKD

UC

No

No

1644/206870

1.00

<0.0001

Yes

804/25457

3.93 (3.61–4.29)***

Yes

No

185/1266

16.5 (14.0–19.4)***

Yes

175/560

57.6 (48.9–67.8)***

CKD

UT-UC

No

No

1644/206870

1.00

<0.0001

Yes

272/4106

8.99 (7.84–10.3)***

Yes

No

185/1266

14.5 (12.3–17.1)***

Yes

58/157

71.5 (54.7–93.5)***

CKD

B-UC

No

No

1644/206870

1.00

<0.0001

Yes

526/21137

3.01 (2.73–3.33)***

Yes

No

185/1266

15.7 (13.3–18.4)***

Yes

116/400

50.6 (41.6–61.6)***

a Multivariate model adjusted for age, sex, geographic region, occupation, monthly income, and comorbidities (diabetes, hypertension, coronary heart disease, atrial fibrillation, heart failure, chronic kidney disease, and hyperlipidemia).

DISCUSSION

This 12-year follow-up study is the first large-scale investigation of the renal outcomes of UC patients in Taiwan, a region that has a high prevalence of UC. There were 3 major findings. First, UC is an independent risk factor for ESRD in male and female patients whether or not they receive nephrouretectomies. Second, women with UT-UC or B-UC have a greater risk for ESRD than men with either UC subtype. Third, patients with UT-UC are more likely to progress to ESRD than those with B-UC, particularly for those with CKD, diabetes, and hypertension.

Our findings confirm that UC patients have a greater risk for ESRD, and this greater risk occurred in those receiving and not receiving nephrouretectomies. Limited information is available on the prognostic impact of UC on renal survival. The total urinary arsenic level is related to CKD risk in a dose-dependent manner with adjustment for age and sex or for multiple risk factors in Taiwan, an area in which blackfoot disease is endemic [12]. The International Agency for Research on Cancer (IARC) classified arsenic as a group I carcinogen because exposure can lead to cancers of the skin, lung, and bladder [13]. Further research is necessary to determine the effect of arsenic exposure on renal survival of UC patients, and whether factors other than inorganic arsenic exposure contribute to the unusually high incidence of UT-UC and ESRD in areas of Taiwan where blackfoot disease is not endemic [14]. Cancer itself is often associated with abnormalities that affect the kidney, and cancer therapy often leads to acute and chronic kidney injury [15]. Furthermore, the marked improvements in cancer therapy have increased the number of cancer survivors, many of whom have residual kidney injury [16, 17].

UT-UC is an independent risk factor for ESRD. A few studies have also shown a significant influence of UT-UC on subsequent ESRD among UC patients [9], possibly because UT-UC may cause more severe obstructive uropathy than B-UC. Gupta et al. reported that B-UC patients with obstructive uropathy, radical cystectomy, and urinary diversion did not have increased risk of ESRD, provided they are adequately prepared before surgery by optimization of renal function [18]. After obstructive uropathy, renal tubular cell injury results from mechanical stretching, ischemia, hypoxia, or exposure to toxins such as oxygen-free radicals. In addition, renal tubular epithelial cells undergo cell death by apoptosis or necrosis, or undergo phenotypic transformation in which they acquire mesenchymal characteristics [19]. If the renal stimulus is transient, these changes can lead to remodeling or regeneration of the tubular epithelium; however, if the insult is severe or prolonged, it may activate a maladaptive response that leads to attraction to the interstitium of inflammatory cells, further damage the tubules, and renal interstitial fibrosis [19]. Our previous findings confirm that patients with CKD, but not necessarily ESRD, have a higher prevalence of UT-UC [4]. This observation is consistent with the close relationship observed here between UT-UC and obstructive uropathy. Moreover, our multivariate analysis indicated that ureteral reimplantation due to obstructive uropathy significantly increased the risk for ESRD (Table 3).

In our series, higher percent of UT-UC patients (22%) did not receive nephroureterectomy. Nephroureterectomy is the gold standard for managing UT-UC. Almost 40% of UT-UC patients receiving nephroureterectomy experienced a perioperative complications, and poor performance status conferred a four-fold greater risk of a perioperative complication [20]. However, many patients with UT-UC who require nephroureterectomy in our study are elderly, comorbid, and at risk for perioperative complications (Table 1). Thus, after survey by urologist, higher percent of UT-UC patients did not receive nephroureterectomy in Taiwan.

The results of the present study indicate that the risk for ESRD was greater in female than male patients with UC, although the reason for the greater risk in females remains unknown. Previous research indicated a greater percentage of females than males prefer alternative therapies, such as Chinese herbs that contain AA. In a Taiwan cohort of 6548 Chinese herbalists, female herbalists had a greater risk for urologic cancers than males (standardized mortality ratio: 3.10; 95% CI = 1.41–5.87) [21]. Recently, Chen et al. reported that patients with AA-induced UT-UC were more likely to be female and to have more advanced renal disease [22]. This may indicate a greater exposure to AA in Taiwanese women or that women are more sensitive to AA [23]. Our data are consistent with recent epidemiologic studies which reported that approximately one-third of the population of Taiwan consumed Chinese medicinal herbs that may contain AA [23-25]. In addition, there is a linear dose–response relationship between consumption of herbal remedies that contain AA with urinary tract cancer [24] and with ESRD [25]. Consistent with their findings, we further showed that UT-UC and B-UC independently increased the risk for ESRD in patients after consumption of AA (Table 2). These epidemiologic studies likely underestimate AA exposure because they only considered Aristolochia-based prescriptions written by physicians over a period of 7 years, and Aristolochia herbs have long been available in Taiwan from alternative sources.

In the study by Chang et al, the authors report that the use of Chinese herbs, especially if they contain AA, may contribute to the development of UC [7]. A population-based study also revealed that the use of AA-containing Chinese herbal products is associated with a dose-dependent increased risk of UC and ESRD [24, 25]. In addition, we found that even segmental ureterectomy, ureteral reimplantation and nephroureterectomy had an increased for ESRD. Therefore, the authors suggest that, in addition to AA induced UC, even segmental ureterectomy, ureteral reimplantation and nephroureterectomy, had an increased risk of ESRD.

Radical cystectomy remains the standard of care for patients with muscle invasive bladder UC. ESRD has traditionally been viewed as a potential long-term consequence of urinary diversion after radical cystectomy because it increases the risk of obstructive uropathy secondary to ureteral-enteric anastomotic stricture or disease recurrence, refiltration of previously excreted toxins that are reabsorbed by the urinary diversion, and upper tract disease recurrence resulting in surgical removal [26]. However, although there was a long-term risk of ESRD after urinary diversion, in our patients with preexisting CKD, there was no significant difference in the development of ESRD in pateints given different types of diversion. Our finding of no significant difference in ESRD risk between conduits, continent cutaneous diversions, and orthotopic neobladders is consistent with that of previous single institution retrospective studies [27]. Future prospective research and alternative measures of renal function would provide more insight into the true risk of renal deterioration after urinary diversion regardless of the type of diversion.

Satasivam et al. found that the patients who possess medical risk factors for CKD are at increased risk of developing progressive renal impairment, despite the use of kidney sparing surgery [28]. More recently, in Capitanio et al’s report, the patients with clinically localized T1abN0M0 renal mass, after accounting for individual baseline characteristics, such as age, diabetes, uncontrolled hypertension, or other comorbidities, showed kidney sparing surgery independently protects against ESRD and the consequent need for dialysis relative to radical nephrectomy [29]. Nevertheless, the authors suggest that, in addition to patients with pre-existing CKD, kidney sparing surgery should be strongly considered in those patients at risk for future renal impairment as predicted by age and medical comorbidities.

This study had the limitations due to the design of the RCIP dataset. First, UC and ESRD diagnoses rely on administrative claims data from physicians or hospitals, and these may be less accurate than those made from standardized criteria. However, the diagnosis of ICD-9 code 188, 189.1, 189.2, or 585 is a serious matter, so physicians generally avoid making such diagnoses unless there is supporting pathological and laboratory reports. Moreover, information on the aggressiveness of UC was not available in the database. Thus, we were unable to measure whether UC aggressiveness was associated with ESRD. Second, this is a retrospective cohort analysis that relied on billing codes to evaluate clinical outcomes, and billing codes can be inconsistent or inaccurate. Information on clinical tests, anthropometric and laboratory examinations, and health-related behaviors of patients (such as smoking and drinking) are not available in the claims data. Thus, we were unable to assess the relationships of laboratory markers, such as hemoglobin or albumin levels, with ESRD. However, the claims data enabled us to perform a natural history study of other comorbidities that may be associated with the renal outcome of patients with UC. Although evaluating CKD stage may be difficult due to inconsistent coding, diagnosis of ESRD that requires dialysis is more clearly associated with medical complications and Medicare reimbursement. In addition, episodes of acute kidney injury during the follow-up period might have increased the accumulated incidence of ESRD in the study and comparison cohorts. However, a major strength of this study is the use of a nationwide population-based sample, because this enabled us to collect representative patients with ESRD. Further long-term follow-up studies that consider other biological and clinical information are needed to elucidate the mechanism of ESRD development in patients with UC.

This large population-based retrospective cohort study suggests that patients with UC have an increased risk for ESRD within approximately 3 to 4 years following cancer diagnosis, and that this increased risk applies to patients receiving and not receiving nephrouretectomies. These relationships should be explored further to identify the possible pathological mechanisms of renal fibrosis and to identify more specific high-risk groups. Surveillance for CKD with renal function testing and ultrasonography may be appropriate for high-risk groups. Patients with UC who also have CKD, diabetes, or hypertension may therefore benefit from early referral to a nephrologist and for long-term follow-up visits.

MATERIALS AND METHODS

Data sources

This retrospective cohort study used the inpatient claims database and Registry for Catastrophic Illness Patients (RCIP), which are parts of the National Health Insurance Research Databases (NHIRD) released by the Taiwan National Health Insurance Administration. This health agency established a universal single-payer insurance program on March 1, 1995, and more than 96% of Taiwan residents had coverage as of 1996. A patient can apply for a claim for a catastrophic illness based on examination of medical records, laboratory studies, and imaging studies by at least two specialists. The databases contain all inpatient claims and insurance information from 1996 to 2010. The identification of insurants was recorded before release. This study was approved by the ethical review board of the China Medical University in Taiwan.

Study subjects

We selected 34,211 patients from the RCIP who had UC (International Classification of Diseases, 9th Revision, Clinical Modification [ICD-9-CM] 188, 189.1-189.0) from 1998 to 2010. The date of UC registry in the RCIP was considered the index date. We excluded patients younger than 25 years and those with a history of another malignancy (ICD-9-CM 140-174, 189.0, 191-208), a history of ESRD (ICD-9-CM 585), or a follow-up duration less than 3 months. Finally, all 26,017 patients with UC (UC cohort) were categorized as having UT-UC (ICD-9-CM 189.1 and 189.2, N = 4263) or bladder UC (B-UC, ICD-9-CM 188, N = 21537). The comparison cohort consisted of individuals with no history of UC before the index date; individuals in this group were randomly matched (8:1) with the UC cohort in terms of age (5 year intervals), sex, index year, and index month. The comparison cohort had the same exclusion criteria as the UC cohort.

Outcome measures

Observed outcome was the incidence of ESRD, those with receiving long-term dialysis (>3 months) and coded as ICD-9-CM 585 in the database. The study variables included sociodemographic characteristics and comorbidities. The sociodemographic variables were sex, age, geographic region of residence (northern, central, southern, and eastern), occupation (white collar, blue collar, and others), and monthly income (based on insurance premium) as less than US$528, US$528–640, and more than US$640 (corresponding to less than NTD15840, NTD15841-20100, and more than NTD20100). The comorbidities were diabetes (ICD-9-CM 250), hypertension (ICD-9-CM 401-405), coronary heart disease (ICD-9-CM 410-414), atrial fibrillation (ICD-9-CM 427.31), heart failure (ICD-9-CM 428), chronic kidney disease (ICD-9-CM 585), hyperlipidemia (ICD-9-CM 272), nephrouretectomy (ICD-9-CM operation code 55.51), and solitary kidney (ICD-9-CM 753.0). In Taiwan, CKD was diagnosed and staged according to the K/DOQI clinical practice guideline [30]. All Taiwanese patients who develop ESRD and require long-term dialysis can apply for catastrophic illness registration cards from the NHI Administration and have no co-payments for health care. The analysis also considered endoscopic treatment of the bladder (78008C, 78049C), radical cystectomy (78011B, 78039B, 78040B, 78012B, 78041B, 78043B, 78042B, 78013B, 78044B, 78014B, 78045B, 78046B), segmental ureterectomy (77003B, 77004B, 77005B, 77006B, 77007B), endoscopic treatment of the ureter (77034B), ureteral reimplantation (50010C, 50019C), conduit diversion (77013B, 77014B, 77015B, 77016B, 77017B), continent cutaneous diversion (77018B, 77019B, 77020B, 77022B), orthotopic neobladder (78012B, 78014B, 78041B, 78045B), and use of AA (A004143, A016919, A019285, A035747, A037982, A044152, A045727, A046081, A046918, A055627, A054560, A002821, A017465, A021356, A034838, A039470, A046913, A047113, A055457, A055646, A006926, A016115, A032033, A032659, A034698, A035728, A039840, A040474, A040904, A043424, A056512, A056413, A034629, A043131, A034629, A034417, A038536, A037415, A035138, A040480, A036897, A031705, A042567, A042787, A039869, A036566, A037455, A034500, A036121, A034497, A032078, A037818, A035116, A037647, A045841, A039113, A043054, A043556, A035907, A042689, A038343, A037459, A035120, A032546, A035725, A032241, A038715, A037113, A036124, A037820, A036989, A037102, A038232). All comorbidities were recorded at admission.

Statistical analysis

Person-years were defined as the interval from the index date to the date of ESRD diagnosis, loss to follow-up, death, or December 31, 2010. We estimated the overall cumulative incidence and incidence by sex, UC, and UC subtype from 1998 to 2010. A chi-square test was used to assess the significance of differences in sociodemographic factors and comorbidities in the comparison and UC cohorts. Kaplan–Meier analysis was employed to plot cumulative incidence curves, and the log-rank test was used to test the significance of differences in these curves between the two groups by sex. Cox proportional hazard regression analysis was used to estimate the risk of ESRD associated with UC and UC subtype. All data analyses were conducted using the SAS 9.3 statistical package for Microsoft Windows (SAS Institute, Cary, NC, USA), and the significance level was set at 0.05, using a two-sided test.

CONFLICTS OF INTEREST

The authors have no conflicts of interest to disclose.

FUNDING

This study is supported in part by Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence (MOHW105-TDU-B-212-133019), China Medical University Hospital (DMR-105-049, CMU102-BC-12), Academia Sinica Taiwan Biobank Stroke Biosignature Project (BM10501010037), NRPB Stroke Clinical Trial Consortium (MOST 104-2325-B-039 -005), Tseng-Lien Lin Foundation, Taichung, Taiwan, Taiwan Brain DiseaseFoundation, Taipei, Taiwan, and Katsuzo and Kiyo AoshimaMemorial Funds, Japan. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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