KIdney aNd blooD prESsure ouTcomes in Childhood Cancer Survivors: Description of Clinical Research Protocol of the KINDEST-CCS Study.

cancer survivors children chronic kidney disease hypertension protocol

Journal

Canadian journal of kidney health and disease
ISSN: 2054-3581
Titre abrégé: Can J Kidney Health Dis
Pays: England
ID NLM: 101640242

Informations de publication

Date de publication:
2022
Historique:
received: 09 09 2022
accepted: 13 09 2022
entrez: 3 11 2022
pubmed: 4 11 2022
medline: 4 11 2022
Statut: epublish

Résumé

Approximately 30% of childhood cancer survivors (CCSs) will develop chronic kidney disease (CKD) or hypertension 15 to 20 years after treatment ends. The incidence of CKD and hypertension in the 5-year window after cancer therapy is unknown. Moreover, extent of monitoring of CCS with CKD and associated complications in current practice is underexplored. To inform the development of new and existing care guidelines for CCS, the epidemiology and monitoring of CKD and hypertension in the early period following cancer therapy warrants further investigation. To describe the design and methods of the KIdney aNd blooD prESsure ouTcomes in Childhood Cancer Survivors study, which aims to evaluate the burden of late kidney and blood pressure outcomes in the first ~10 years after cancer therapy, the extent of appropriate screening and complications monitoring for CKD and hypertension, and whether patient, disease/treatment, or system factors are associated with these outcomes. Two distinct, but related studies; a prospective cohort study and a retrospective cohort study. Five Ontario pediatric oncology centers. The prospective study will involve 500 CCS at high risk for these late effects due to cancer therapy, and the retrospective study involves 5,000 CCS ≤ 18 years old treated for cancer between January 2008 and December 2020. Chronic kidney disease is defined as Estimated glomerular filtration rate <90 mL/min/1.73 m Prospective study: we aim to investigate CKD and hypertension prevalence and the extent to which they persist at 3- and 5-year follow-up in CCS after cancer therapy. We will collect detailed biologic and clinical data, calculate CKD and hypertension prevalence, and progression at 3- and 5-years post-therapy. Retrospective study: we aim to investigate CKD and hypertension monitoring using administrative and health record data. We will also investigate the validity of CKD and hypertension administrative definitions in this population and the incidence of CKD and hypertension in the first ~10 years post-cancer therapy. We will investigate whether patient-, disease/treatment-, or system-specific factors modify these associations in both studies. Results from the prospective study may not be generalizable to non-high-risk CCS. The retrospective study is susceptible to surveillance bias. Our team and knowledge translation plan is engaging patient partners, researchers, knowledge users, and policy group representatives. Our work will address international priorities to improve CCS health, provide the evidence of new disease burden and practice gaps to improve CCS guidelines, implement and test revised guidelines, plan trials to reduce CKD and hypertension, and improve long-term CCS health.

Sections du résumé

Background UNASSIGNED
Approximately 30% of childhood cancer survivors (CCSs) will develop chronic kidney disease (CKD) or hypertension 15 to 20 years after treatment ends. The incidence of CKD and hypertension in the 5-year window after cancer therapy is unknown. Moreover, extent of monitoring of CCS with CKD and associated complications in current practice is underexplored. To inform the development of new and existing care guidelines for CCS, the epidemiology and monitoring of CKD and hypertension in the early period following cancer therapy warrants further investigation.
Objective UNASSIGNED
To describe the design and methods of the KIdney aNd blooD prESsure ouTcomes in Childhood Cancer Survivors study, which aims to evaluate the burden of late kidney and blood pressure outcomes in the first ~10 years after cancer therapy, the extent of appropriate screening and complications monitoring for CKD and hypertension, and whether patient, disease/treatment, or system factors are associated with these outcomes.
Design UNASSIGNED
Two distinct, but related studies; a prospective cohort study and a retrospective cohort study.
Setting UNASSIGNED
Five Ontario pediatric oncology centers.
Patients UNASSIGNED
The prospective study will involve 500 CCS at high risk for these late effects due to cancer therapy, and the retrospective study involves 5,000 CCS ≤ 18 years old treated for cancer between January 2008 and December 2020.
Measurements UNASSIGNED
Chronic kidney disease is defined as Estimated glomerular filtration rate <90 mL/min/1.73 m
Methods UNASSIGNED
Prospective study: we aim to investigate CKD and hypertension prevalence and the extent to which they persist at 3- and 5-year follow-up in CCS after cancer therapy. We will collect detailed biologic and clinical data, calculate CKD and hypertension prevalence, and progression at 3- and 5-years post-therapy. Retrospective study: we aim to investigate CKD and hypertension monitoring using administrative and health record data. We will also investigate the validity of CKD and hypertension administrative definitions in this population and the incidence of CKD and hypertension in the first ~10 years post-cancer therapy. We will investigate whether patient-, disease/treatment-, or system-specific factors modify these associations in both studies.
Limitations UNASSIGNED
Results from the prospective study may not be generalizable to non-high-risk CCS. The retrospective study is susceptible to surveillance bias.
Conclusions UNASSIGNED
Our team and knowledge translation plan is engaging patient partners, researchers, knowledge users, and policy group representatives. Our work will address international priorities to improve CCS health, provide the evidence of new disease burden and practice gaps to improve CCS guidelines, implement and test revised guidelines, plan trials to reduce CKD and hypertension, and improve long-term CCS health.

Identifiants

pubmed: 36325265
doi: 10.1177/20543581221130156
pii: 10.1177_20543581221130156
pmc: PMC9618744
doi:

Types de publication

Journal Article

Langues

eng

Pagination

20543581221130156

Informations de copyright

© The Author(s) 2022.

Déclaration de conflit d'intérêts

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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Auteurs

Adree Khondker (A)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Temerty Faculty of Medicine, University of Toronto, ON, Canada.

Michael Groff (M)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Department of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Canada.

Sophia Nunes (S)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Carolyn Sun (C)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Natasha Jawa (N)

Division of Nephrology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Jasmine Lee (J)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Vedran Cockovski (V)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Yasmine Hejri-Rad (Y)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Rahul Chanchlani (R)

Department of Pediatrics, McMaster Children's Hospital, Hamilton, ON, Canada.

Adam Fleming (A)

Department of Pediatric Hematology/Oncology, McMaster Children's Hospital, Hamilton, ON, Canada.

Amit Garg (A)

Department of Medicine, London Health Sciences Centre Research Inc., London, ON, Canada.

Nivethika Jeyakumar (N)

Institute of Clinical Evaluative Sciences Western, London, ON, Canada.

Abhijat Kitchlu (A)

Division of Nephrology, Department of Medicine, University of Toronto, ON, Canada.

Asaf Lebel (A)

Division of Nephrology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Eric McArthur (E)

Institute for Clinical Evaluative Sciences, Toronto, ON, Canada.

Luc Mertens (L)

Division of Cardiology, The Labatt Family Heart Center, The Hospital for Sick Children, Toronto, ON, Canada.

Paul Nathan (P)

Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Rulan Parekh (R)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Division of Nephrology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Serina Patel (S)

Department of Pediatric Hematology/Oncology, Children's Hospital of Western Ontario, London, Canada.

Jason Pole (J)

Pediatric Oncology Group of Ontario, Toronto, Canada.

Raveena Ramphal (R)

Department of Pediatrics, Children's Hospital of Eastern Ontario-Ottawa Children's Treatment Centre, Canada.

Tal Schechter (T)

Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Mariana Silva (M)

Department of Pediatrics, Kingston Health Sciences Centre, ON, Canada.

Samuel Silver (S)

Division of Nephrology, Department of Medicine, Queen's University, Kingston, ON, Canada.

Lillian Sung (L)

Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Ron Wald (R)

Unity Health Toronto, ON, Canada.

Paul Gibson (P)

Pediatric Oncology Group of Ontario, Toronto, Canada.

Rachel Pearl (R)

William Osler Health System, Brampton, ON, Canada.

Laura Wheaton (L)

Department of Pediatrics, Kingston Health Sciences Centre, ON, Canada.

Peter Wong (P)

William Osler Health System, Brampton, ON, Canada.

Kirby Kim (K)

Patient Partner, The Hospital for Sick Children, Toronto, ON, Canada.

Michael Zappitelli (M)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Division of Nephrology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

Classifications MeSH