Evidence mapPaperPMID 40388170Full record

ArticleJAMA network open2025

Chronic Kidney Disease or Hypertension After Childhood Cancer.

Asaf Lebel, Rahul Chanchlani, Vedran Cockovski, Allison Dart, Adam James Fleming, Amit X Garg, Nivethika Jeyakumar, Kirby Kim, Abhijat Kitchlu, Eric McArthur and 13 more

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Asaf LebelDivision of Nephrology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Rahul ChanchlaniDivision of Pediatric Nephrology, Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Vedran CockovskiDivision of Nephrology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Allison DartDepartment of Pediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba, Canada.
Adam James FlemingDepartment of Pediatric Hematology and Oncology, McMaster Children's Hospital, Hamilton, Ontario, Canada.
Amit X GargLondon Health Sciences Centre, Lawson Health Research Institute, London, Ontario, Canada.
Nivethika JeyakumarLondon Health Sciences Centre, Lawson Health Research Institute, London, Ontario, Canada.
Kirby KimPatient Partner, The Hospital for Sick Children, Toronto, Ontario, Canada.
Abhijat KitchluDivision of Nephrology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Eric McArthurLondon Health Sciences Centre, Lawson Health Research Institute, London, Ontario, Canada.
Danielle NashLondon Health Sciences Centre, Lawson Health Research Institute, London, Ontario, Canada.
Paul C NathanDivision of Haematology and Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Rulan S ParekhDivision of Nephrology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Rachel PearlDivision of Nephrology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Jason PolePediatric Oncology Group of Ontario, Toronto, Ontario, Canada.
Raveena RamphalDivision of Hematology and Oncology, Department of Pediatrics, Children's Hospital of Eastern Ontario-Ottawa Children's Treatment Centre, Ottawa, Ontario, Canada.
Jennifer ReidLondon Health Sciences Centre, Lawson Health Research Institute, London, Ontario, Canada.
Tal Schechter-FinkelsteinDivision of Haematology and Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Lillian SungDivision of Haematology and Oncology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Ron WaldDivision of Nephrology, St Michael's Hospital and University of Toronto, Toronto, Ontario, Canada.
Stella WangDivision of Nephrology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Peter WongWilliam Osler Health System, Brampton, Ontario, Canada.
Michael ZappitelliDivision of Nephrology, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.

Funding

CIHR
6 · The paper itself

Abstract

Importance: Post-cancer therapy kidney outcomes, including chronic kidney disease (CKD) and hypertension, are common in childhood cancer survivors (CCS). The incidence and timing of CKD and hypertension in CCS compared with other at-risk or general populations are unclear. Objective: To determine the association of childhood cancer treatment with post-cancer therapy CKD or hypertension. Design, Setting, and Participants: Population-based matched cohort study of children treated for cancer between April 1993 and March 2020 in Ontario, Canada, with follow-up until March 2021. The CCS (exposed) cohort included children (≤18 years) surviving cancer. Comparator cohorts were a hospitalization cohort (children who were hospitalized) and a general pediatric population (GP) cohort (all other Ontario children). Exclusion criteria were history of previous cancer, organ transplant, CKD, dialysis, or hypertension. Matching with each of the 2 comparator cohorts was performed separately and in a 1:4 ratio by age, sex, rural vs urban status, income quintile, index year, and presence of previous hospitalization. Data were analyzed from March 2021 to August 2024. Exposure: Treatment for cancer. Main Outcomes and Measures: The primary outcome was the composite of CKD or hypertension, defined by administrative health care diagnosis and procedure codes. Fine and Gray subdistribution hazard modeling, accounting for competing risks (death and new cancer diagnosis or relapse) and adjusting for cardiac disease, liver disease, and diabetes, was used to determine the association of cancer treatment with outcomes. Results: There were 10 182 CCS (median [IQR] age at diagnosis, 7 [3-13] years; 5529 male [54.3%]; median [IQR] follow-up time, 8 [2-15] years) matched to 40 728 hospitalization cohort patients (median [IQR] age at diagnosis, 7 [2-12] years; 5529 male [weighted percentage, 54.3%]; median [IQR] follow-up time, 11 [6-18] years) and 8849 CCS (median [IQR] age at diagnosis, 5 [2-11] years; 4825 male [54.5%]; median [IQR] follow-up time, 7 [2-14] years) matched to 35 307 GP cohort individuals (median [IQR] age at diagnosis, 6 [2-11] years; 4825 male [weighted percentage, 54.5%]; median [IQR] follow-up time, 10 [5-16] years). Most frequent cancer types were leukemia (2948 patients [29.0%]), central nervous system neoplasms (2123 patients [20.9%]), and lymphoma (1583 patients [15.5%]). During observation, cumulative incidence of CKD or hypertension was 20.85% (95% CI, 18.75%-23.02%) in the CCS cohort vs 16.47% (95% CI, 15.21%-17.77%) in the hospitalization cohort and 19.24% (95% CI, 15.99%-22.73%) in the CCS cohort vs 8.05% (95% CI, 6.76%-9.49%) in the GP cohort. CCS were at increased risk of CKD or hypertension compared with the hospitalization cohort (adjusted hazard ratio, 2.00; 95% CI, 1.86-2.14; P < .001) and the GP cohort (adjusted hazard ratio, 4.71; 95% CI, 4.27-5.19; P < .001). Conclusions and Relevance: In this population-based study, CCS were at increased risk for CKD and hypertension, which are associated with mortality, suggesting that early detection and treatment of these conditions in CCS may decrease late complications and mortality.

Indexed as

Cancer SurvivorsHypertensionNeoplasmsRenal Insufficiency, ChronicAdolescentChildChild, PreschoolCohort StudiesFemaleHumansIncidenceInfantMaleOntarioRisk Factors

Identifiers

PMID40388170
PMCPMC12090035

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.