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

Sponsor
The Hospital for Sick Children (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06153147
Collaborator
(none)
500
191.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase

    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.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    KIdney aNd blooD prESsure ouTcomes in Childhood Cancer Survivors (CCS): Prospective Study
    Anticipated Study Start Date :
    Jan 5, 2024
    Anticipated Primary Completion Date :
    Oct 25, 2029
    Anticipated Study Completion Date :
    Dec 31, 2039

    Arms and Interventions

    Arm Intervention/Treatment
    Late effects after nephrotoxic chemotherapies.

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

    Outcome Measures

    Primary Outcome Measures

    1. Prevalence of Chronic Kidney Disease (CKD) based on eGFR (using an equation) at 3 years post cancer therapy [3 years +/- 6 months after cancer therapy end]

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

    2. Prevalence of Chronic Kidney Disease (CKD) based on eGFR (using an equation) at 5 years post cancer therapy [5 years +/- 6 months after cancer therapy end]

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

    3. Prevalence of Hypertension (HTN) from office blood pressure (vis blood pressure machine) at 3 years post cancer therapy [3 years +/- 6 months after cancer therapy end]

      Defined by 2017 American Academy of Pediatrics (AAP) guidelines

    4. Prevalence of Hypertension (HTN) using Ambulatory Blood Pressure Measurement (ABPM) at 5 years post cancer therapy [5 years +/- 6 months after cancer therapy end]

      The presence of either ambulatory hypertension or masked hypertension

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

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

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

      Change in albuminuria in mg/g

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

      Change in proteinuria in mg/mmol

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

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

    Secondary Outcome Measures

    1. Impact of Acute Kidney Injury (AKI) and Cardiometabolic risk factors (using blood work) at baseline on CKD outcomes [At baseline for independent factors on CKD outcomes at 3 and 5 years]

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

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 19 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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:
    • Pre-cancer severe CKD and/or previous kidney transplant

    • 19 years old at 3 years after cancer therapy completion

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • The Hospital for Sick Children

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Michael Zappitelli, Staff Nephrologist and Senior Scientist, The Hospital for Sick Children
    ClinicalTrials.gov Identifier:
    NCT06153147
    Other Study ID Numbers:
    • OCREB 4177
    First Posted:
    Dec 1, 2023
    Last Update Posted:
    Dec 1, 2023
    Last Verified:
    Nov 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 1, 2023