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RecruitingNCT06153147KINDEST-CCSUpdated Apr 17, 2024

KIdney aNd blooD prESsure ouTcomes in Childhood Cancer Survivors (CCS)

An observational study in Childhood Cancer, Chronic Kidney Diseases and Hypertension, sponsored by The Hospital for Sick Children. Recruiting at 1 site in Canada. Open to participants aged Up to 19 Years. Per ClinicalTrials.gov, last updated 2024-04-17.

Sponsored by The Hospital for Sick Children · Observational

From the registry’s dates

  • Started Jan 2024; still recruiting 2 years 9 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
Up to 19 Years
Sex
All
01

Study summary

Background: Childhood cancer survivors (CCS) are at elevated risk of chronic health conditions. Chemotherapies can cause recurrent acute kidney injury which may progress to kidney fibrosis, chronic kidney disease (CKD) or hypertension (HTN). CCS surviving to adulthood are at ≥3 times the risk (vs. non-CCS) for CKD, HTN and lower quality of life. However, the timing of CKD and HTN onset in CCS completing cancer therapy in childhood remains unclear.

Guidelines provide recommendations on managing post-cancer therapy effects in CCS, but they lack specificity on kidney testing content, frequency and complications. This discord is largely due to knowledge gaps on which CCS develop CKD or HTN after cancer therapy, when outcomes occur and their severity. Existing work has shown in select patients, CKD and HTN in CCS likely begins in the first 5 years post-cancer therapy and that the burden is significant. With robust data on CKD and HTN, international CCS follow-up guidelines can be optimized to include detailed and actionable recommendations on kidney and blood pressure monitoring and treatment.

Read the detailed description

Significant improvements in childhood cancer survival rates have come at the cost of an increase in chronic health conditions. Childhood cancer survivors (CCS) often experience chronic kidney disease (CKD) and hypertension (HTN), yet data on the onset and severity of these diseases in the primary years after childhood cancer therapy is unclear. Both CKD and HTN are major treatable cardiovascular risk factors, and the knowledge gap in the first 5 years after therapy impedes the creation of evidence-based guidelines and early intervention plans.

Currently, the Children's Oncology Group international guidelines, which are used to identify and manage therapy effects in CCS, lack information on CKD testing and appropriate measures. With appropriate treatment, CKD and HTN complications are treatable.

In 500 CCS at high risk for blood pressure (BP) and late kidney effects due to cancer therapy, we will determine the prevalence of HTN and CKD at 3 and 5 years after cancer therapy, and the extent to which eGFR, albuminuria and BP worsen from 3 to 5 years after therapy. In addition, we will assess whether acute kidney injury during cancer therapy and cardiometabolic risk factors are associated with these outcomes.

Based on the evidence from the study, we hope to improve current CCS kidney and BP guidelines to advise on appropriate treatments and measures for HTN and CKD. As CCS are vulnerable to cardiovascular disease, addressing CKD and HTN complications will improve their overall quality of life.

02

Conditions studied

  • Childhood Cancer
  • Chronic Kidney Diseases
  • Hypertension
  • Acute Kidney Injury
  • Nephrotoxicity
03

In context

Neoplasms

9,610 studies on the registry are indexed under Neoplasms; 2,508 are open to participants now.

This study's planned enrollment of 500 is above the median of 202 across 1,742 observational studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

The Hospital for Sick Children is the lead sponsor of 577 studies on the registry; 83 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Up to 19 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Observational cohort study of CCS at 5 Ontario child cancer centres

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 3 years ± 6 months after therapy for first cancer
  • Received high-risk therapy for first cancer, as defined by the Canadian Oncology Group (COG) as alkylating agents; platinums; abdominal or total body radiation; high dose methotrexate; stem cell transplant; nephrectomy; or other therapy which may be known to possibly cause late kidney and/or BP effects.

Exclusion criteria

Exclusion Criteria:

  • Pre-cancer severe CKD and/or previous kidney transplant
  • >19 years old at 3 years after cancer therapy completion
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Late effects after nephrotoxic chemotherapies.

    3 and 5 year kidney and blood pressure effects after cancer therapy.

06

What researchers measure

Primary outcomes

  1. Prevalence of Chronic Kidney Disease (CKD) based on eGFR (using an equation) at 3 years post cancer therapy

    CKD: Per Kidney Disease Improving Global Outcomes (KDIGO) guidelines

    Time frame: 3 years +/- 6 months after cancer therapy end

  2. Prevalence of Chronic Kidney Disease (CKD) based on eGFR (using an equation) at 5 years post cancer therapy

    CKD: Per Kidney Disease Improving Global Outcomes (KDIGO) guidelines

    Time frame: 5 years +/- 6 months after cancer therapy end

  3. Prevalence of Hypertension (HTN) from office blood pressure (vis blood pressure machine) at 3 years post cancer therapy

    Defined by 2017 American Academy of Pediatrics (AAP) guidelines

    Time frame: 3 years +/- 6 months after cancer therapy end

  4. Prevalence of Hypertension (HTN) using Ambulatory Blood Pressure Measurement (ABPM) at 5 years post cancer therapy

    The presence of either ambulatory hypertension or masked hypertension

    Time frame: 5 years +/- 6 months after cancer therapy end

  5. Change in markers of kidney health (eGFR)(using an equation) between 3 and 5 years post cancer therapy

    Change in eGFR in milliliter (mL) /min/1.73m2

    Time frame: Change from 3 to 5 years in eGFR

  6. Change in markers of kidney health (Albuminuria) (using lab values) between 3 and 5 years post cancer therapy

    Change in albuminuria in mg/g

    Time frame: Change from 3 to 5 years in Albuminuria

  7. Change in markers of kidney health (Proteinuria) (using Lab values) between 3 and 5 years post cancer therapy

    Change in proteinuria in mg/mmol

    Time frame: Change from 3 to 5 years in Proteinuria

  8. Change in markers of cardiovascular health (using blood tests) between 3 and 5 years post cancer therapy

    Change in BP percentile as per 2017 American Academy of Pediatrics (AAP) guidelines

    Time frame: Change from 3 to 5 years

Secondary outcomes

  1. Impact of Acute Kidney Injury (AKI) and Cardiometabolic risk factors (using blood work) at baseline on CKD outcomes

    CKD: Per Kidney Disease Improving Global Outcomes (KDIGO) guidelines

    Time frame: At baseline for independent factors on CKD outcomes at 3 and 5 years

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06153147
Responsible party
Michael Zappitelli (Staff Nephrologist and Senior Scientist, The Hospital for Sick Children) — Principal investigator
First posted
Dec 1, 2023
Start date
Jan 5, 2024
Primary completion
Oct 25, 2029 (estimated)
Completion
Dec 31, 2039 (estimated)
Last update
Apr 17, 2024

Study contacts

Michael Zappitelli, MD
Contact
michael.zappitelli@sickkids.ca
4168137605 ext. 304077
Yasmine Hejri-Rad, BA
Contact
yasmine.hejri-rad@sickkids.ca
416-813-7605 ext. 309031

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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