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

Author:

Khondker Adree12,Groff Michael13,Nunes Sophia1,Sun Carolyn1,Jawa Natasha4,Lee Jasmine1,Cockovski Vedran1,Hejri-Rad Yasmine1,Chanchlani Rahul5,Fleming Adam6,Garg Amit7ORCID,Jeyakumar Nivethika8,Kitchlu Abhijat9,Lebel Asaf4,McArthur Eric10,Mertens Luc11,Nathan Paul12,Parekh Rulan14,Patel Serina13,Pole Jason14,Ramphal Raveena15,Schechter Tal12,Silva Mariana16,Silver Samuel17ORCID,Sung Lillian12,Wald Ron18,Gibson Paul14,Pearl Rachel19,Wheaton Laura16,Wong Peter19,Kim Kirby20,Zappitelli Michael14ORCID

Affiliation:

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

2. Temerty Faculty of Medicine, University of Toronto, ON, Canada

3. Department of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Canada

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

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

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

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

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

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

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

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

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

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

14. Pediatric Oncology Group of Ontario, Toronto, Canada

15. Department of Pediatrics, Children’s Hospital of Eastern Ontario–Ottawa Children’s Treatment Centre, Canada

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

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

18. Unity Health Toronto, ON, Canada

19. William Osler Health System, Brampton, ON, Canada

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

Abstract

Background: 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: 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: Two distinct, but related studies; a prospective cohort study and a retrospective cohort study. Setting: Five Ontario pediatric oncology centers. Patients: 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: Chronic kidney disease is defined as Estimated glomerular filtration rate <90 mL/min/1.73 m2 or albumin-to-creatinine ratio ≥ 3mg/mmol. Hypertension is defined by 2017 American Academy of Pediatrics guidelines. Methods: 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: Results from the prospective study may not be generalizable to non-high-risk CCS. The retrospective study is susceptible to surveillance bias. Conclusions: 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.

Funder

Institute of Human Development, Child and Youth Health

Publisher

SAGE Publications

Subject

Nephrology

Reference72 articles.

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