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. Author manuscript; available in PMC: 2013 Aug 1.
Published in final edited form as: Pediatr Nephrol. 2012 Mar 20;27(8):1325–1333. doi: 10.1007/s00467-012-2140-x

Table 2.

National Wilms Tumor Study (NWTS) patient characteristics by end stage renal disease (ESRD) type

Patient characteristic ESRD-PBWT ESRD-CRF All ESRD
No % No % No %
Gender
Male 28 50.9 54 45.8 82 47.4
Female 27 49.1 64 54.2 91 52.6
Ethnicity
White, non-Hispanic 37 67.3 80 67.8 117 67.6
African 11 20.0 16 13.6 27 15.6
Hispanic 6 10.9 16 13.6 22 12.7
Other 1 1.8 6 5.1 7 4.0
Age at ESRD (years)
0–4 33 50.0 32 27.1 65 37.6
5–9 16 29.1 11 9.3 27 15.6
10–14 3 5.5 16 13.6 19 11.0
15–19 2 3.6 17 14.4 19 11.0
20–24 1 1.8 26 22.0 27 15.6
25+ 0 0.0 16 13.6 16 9.2
Congenital syndrome
DDS 1 1.8 28 23.7 29 16.8
WAGR 1 1.8 14 11.9 15 8.8
GU 6 10.9 13 11.0 19 11.0
None 47 85.5 63 53.4 110 63.6
Onset of ESRD
Before WT diagnosis 0 0.0 8 6.8 8 4.6
During WT treatment 27 49.1 16 13.6 43 30.9
During remission 28 50.9 94 79.7 122 70.5
Laterality of WT
Unilateral 0 0.0 89 75.4 89 51.4
Synchronous bilateral 37 67.3 26 22.0 63 36.4
Metachronous bilateral 18 32.7 3 2.5 21 12.1
Initial ESRD treatment
Peritoneal dialysis 24 42.9 41 34.7 65 37.6
Hemodialysis 28 51.8 56 47.5 84 48.6
Dialysis (unspecified) 3 5.4 3 2.5 6 3.7
Preemptive Transplant 0 0.0 18 15.2 18 10.4
Cause of death
WT/Rx 23 41.8 7 5.9 30 17.3
ESRD 7 12.7 19 16.1 26 15.0
Other 3 5.5 4 3.4 7 4.0
Still living 22 40.0 88 74.5 110 63.6

PBWT progressive bilateral Wilms tumor; CRF chronic renal failure; DDS Denys-Drash syndrome; WAGR Wilms tumor, aniridia, genitourinary anomalies, retardation; WT Wilms tumor; GU genitourinary