Literature DB >> 21683387

Risk factors for end stage renal disease in non-WT1-syndromic Wilms tumor.

Jane Lange1, Susan M Peterson, Janice R Takashima, Yevgeny Grigoriev, Michael L Ritchey, Robert C Shamberger, J Bruce Beckwith, Elizabeth Perlman, Daniel M Green, Norman E Breslow.   

Abstract

PURPOSE: We assessed risk factors for end stage renal disease in patients with Wilms tumor without known WT1 related syndromes. We hypothesized that patients with characteristics suggestive of a WT1 etiology (early onset, stromal predominant histology, intralobar nephrogenic rests) would have a higher risk of end stage renal disease due to chronic renal failure. We predicted a high risk of end stage renal disease due to progressive bilateral Wilms tumor in patients with metachronous bilateral disease.
MATERIALS AND METHODS: End stage renal disease was ascertained in 100 of 7,950 nonsyndromic patients enrolled in a National Wilms Tumor Study during 1969 to 2002. Risk factors were evaluated with cumulative incidence curves and proportional hazard regressions.
RESULTS: The cumulative incidence of end stage renal disease due to chronic renal failure 20 years after Wilms tumor diagnosis was 0.7%. For end stage renal disease due to progressive bilateral Wilms tumor the incidence was 4.0% at 3 years after diagnosis in patients with synchronous bilateral Wilms tumor and 19.3% in those with metachronous bilateral Wilms tumor. For end stage renal disease due to chronic renal failure stromal predominant histology had a HR of 6.4 relative to mixed (95% CI 3.4, 11.9; p<0.001), intralobar rests had a HR of 5.9 relative to no rests (95% CI 2.0, 17.3; p=0.001), and Wilms tumor diagnosis at less than 24 months had a HR of 1.7 relative to 24 to 48 months and 2.8 relative to greater than 48 months (p=0.003 for trend).
CONCLUSIONS: Metachronous bilateral Wilms tumor is associated with high rates of end stage renal disease due to surgery for progressive Wilms tumor. Characteristics associated with a WT1 etiology markedly increased the risk of end stage renal disease due to chronic renal failure despite the low risk in non-WT1 syndromic cases overall.
Copyright © 2011 American Urological Association Education and Research, Inc. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21683387      PMCID: PMC3133859          DOI: 10.1016/j.juro.2011.03.110

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  35 in total

Review 1.  Wilms tumor genetics.

Authors:  V Huff
Journal:  Am J Med Genet       Date:  1998-10-02

2.  Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.

Authors:  V Schumacher; K Schärer; E Wühl; H Altrogge; K E Bonzel; M Guschmann; T J Neuhaus; R M Pollastro; E Kuwertz-Bröking; M Bulla; A M Tondera; P Mundel; U Helmchen; R Waldherr; A Weirich; B Royer-Pokora
Journal:  Kidney Int       Date:  1998-06       Impact factor: 10.612

3.  Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

Authors:  B Klamt; A Koziell; F Poulat; P Wieacker; P Scambler; P Berta; M Gessler
Journal:  Hum Mol Genet       Date:  1998-04       Impact factor: 6.150

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Authors:  K Pritchard-Jones
Journal:  Crit Rev Oncog       Date:  1997

5.  Renal salvage procedures in patients with synchronous bilateral Wilms' tumors: a report from the National Wilms' Tumor Study Group.

Authors:  J R Horwitz; M L Ritchey; J Moksness; N E Breslow; G R Smith; P R Thomas; G Haase; R C Shamberger; J B Beckwith
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Review 6.  Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.

Authors:  R H Scott; C A Stiller; L Walker; N Rahman
Journal:  J Med Genet       Date:  2006-05-11       Impact factor: 6.318

7.  Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.

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Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

8.  Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study.

Authors:  Suzanne E Little; Sandra P Hanks; Linda King-Underwood; Chris Jones; Elizabeth A Rapley; Nazneen Rahman; Kathy Pritchard-Jones
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Review 9.  Histological analysis of aggressiveness and responsiveness in Wilms' tumor.

Authors:  J B Beckwith; C E Zuppan; N G Browning; J Moksness; N E Breslow
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10.  International variations in the incidence of childhood renal tumours.

Authors:  C A Stiller; D M Parkin
Journal:  Br J Cancer       Date:  1990-12       Impact factor: 7.640

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2.  Renal function in survivors of nonsyndromic Wilms tumor treated with unilateral radical nephrectomy.

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3.  Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.

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Review 4.  Nephron-sparing surgery for bilateral Wilms tumor.

Authors:  Kathleen Kieran; Andrew M Davidoff
Journal:  Pediatr Surg Int       Date:  2015-01-30       Impact factor: 1.827

5.  Treatments and outcomes for end-stage renal disease following Wilms tumor.

Authors:  Yevgeny Grigoriev; Jane Lange; Susan M Peterson; Janice R Takashima; Michael L Ritchey; Dicken Ko; James H Feusner; Robert C Shamberger; Daniel M Green; Norman E Breslow
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6.  Long-term renal function after treatment for unilateral, nonsyndromic Wilms tumor. A report from the St. Jude Lifetime Cohort Study.

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Journal:  Cancer       Date:  2020-05-27       Impact factor: 6.860

Review 9.  Oncology: the role of partial nephrectomy in Wilms tumor.

Authors:  Miriam Harel; John H Makari; Fernando A Ferrer
Journal:  Curr Urol Rep       Date:  2013-08       Impact factor: 3.092

Review 10.  Innovations in the management of Wilms' tumor.

Authors:  Joseph M Gleason; Armando J Lorenzo; Paul R Bowlin; Martin A Koyle
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