Long-term renal function after treatment for unilateral, nonsyndromic Wilms tumor. A report from the St. Jude Lifetime Cohort Study.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
10 2020
Historique:
received: 16 10 2019
revised: 02 03 2020
accepted: 03 03 2020
pubmed: 25 7 2020
medline: 1 1 2021
entrez: 25 7 2020
Statut: ppublish

Résumé

The impact of specific treatment modalities on long-term renal function and blood pressure among adult survivors of Wilms tumor (WT) has not been well documented. Among 40 WT survivors and 35 noncancer controls, we estimated the glomerular filtration rate (eGFR) using the Chronic Kidney Disease-Epidemiology (CKD-EPI) equations with and without cystatin C, obtained 24-hour ambulatory blood pressure readings, and, among survivors only, measured Twenty-six (65%) WT survivors were female, and 33 (83%) were non-Hispanic white. GFR estimated with creatinine or creatinine + cystatin C was decreased among irradiated survivors compared with controls. No irradiated or unirradiated participant had an eGFR (creatinine + cystatin C) < 60 mL/min/1.73 m Chronic kidney disease was infrequent in long-term survivors of unilateral nonsyndromic WT, whether treated with WART or no radiation. The prevalence of hypertension was increased in both groups compared with controls, emphasizing the need for ongoing monitoring of renal and cardiovascular health.

Sections du résumé

BACKGROUND
The impact of specific treatment modalities on long-term renal function and blood pressure among adult survivors of Wilms tumor (WT) has not been well documented.
METHODS
Among 40 WT survivors and 35 noncancer controls, we estimated the glomerular filtration rate (eGFR) using the Chronic Kidney Disease-Epidemiology (CKD-EPI) equations with and without cystatin C, obtained 24-hour ambulatory blood pressure readings, and, among survivors only, measured
RESULTS
Twenty-six (65%) WT survivors were female, and 33 (83%) were non-Hispanic white. GFR estimated with creatinine or creatinine + cystatin C was decreased among irradiated survivors compared with controls. No irradiated or unirradiated participant had an eGFR (creatinine + cystatin C) < 60 mL/min/1.73 m
CONCLUSIONS
Chronic kidney disease was infrequent in long-term survivors of unilateral nonsyndromic WT, whether treated with WART or no radiation. The prevalence of hypertension was increased in both groups compared with controls, emphasizing the need for ongoing monitoring of renal and cardiovascular health.

Identifiants

pubmed: 32706494
doi: 10.1002/pbc.28271
pmc: PMC7735383
mid: NIHMS1639993
doi:

Substances chimiques

Biomarkers 0
Creatinine AYI8EX34EU

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e28271

Subventions

Organisme : NCI NIH HHS
ID : CA21765
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA021765
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA195547
Pays : United States
Organisme : NCI NIH HHS
ID : CA195547
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 Wiley Periodicals, Inc.

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Auteurs

Daniel M Green (DM)

Department of Epidemiology and Cancer Control, and Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Mingjuan Wang (M)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.

Matthew J Krasin (MJ)

Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Andrew M Davidoff (AM)

Department of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee.

DeoKumar Srivastava (D)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.

Dennis W Jay (DW)

Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Kirsten K Ness (KK)

Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

Barry L Shulkin (BL)

Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee.

Sheri L Spunt (SL)

Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Deborah P Jones (DP)

Department of Pediatrics, University of Tennessee College of Medicine, Memphis, Tennessee.

Jennifer Q Lanctot (JQ)

Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

Kyla C Shelton (KC)

Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

Rachel C Brennan (RC)

Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, and Department of Ophthalmology, University of Tennessee College of Medicine, Memphis, Tennessee.

Daniel A Mulrooney (DA)

Department of Epidemiology and Cancer Control, and Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, and the Department of Pediatrics, University of Tennessee College of Medicine, Memphis, Tennessee.

Matthew J Ehrhardt (MJ)

Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

Todd M Gibson (TM)

Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

Beth A Kurt (BA)

Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Leslie L Robison (LL)

Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee.

Melissa M Hudson (MM)

Department of Epidemiology and Cancer Control, and Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, and the Department of Pediatrics, University of Tennessee College of Medicine, Memphis, Tennessee.

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