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Medical assessment of adverse health outcomes in Dutch childhood cancer survivors; a nationwide project; DCOG-LATER Q2008 study; Long-term renal effects in Dutch survivors of childhood cancer

Medical assessment of adverse health outcomes in Dutch childhood cancer survivors; a nationwide project; DCOG-LATER Q2008 study; Long-term renal effects in Dutch survivors of childhood cancer - DCOG- LATER Q2008 - renal

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47761
Enrollment
2000
Registered
2015-01-23
Start date
2016-05-04
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

late nefrotoxic effects of treatment for childhood cancer renal damage in long-term survivors of childhood cancer

Interventions

None listed

Sponsors

Stichting Kinderoncologie Nederland
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients who were treated for childhood cancer (before age 18) in one of the seven Pediatric Oncology Centers between 1960 and 2004 and who survived for at least 5 years after diagnosis will be included in the SKION LATER study. Participating centres are located in Amsterdam (VU University Medical Center (VUMC)), Groningen (Children's Cancer Center/ University Medical Center Groningen (UMCG)), Rotterdam (Rotterdam Erasmus MC-Sophia (REMC-S), Nijmegen (University Medical Center Nijmegen (UMCN)), Leiden (Leiden University Medical Center (LUMC) and Utrecht (Princess Máxima Center for Pediatric Oncology (PMC)). From this cohort, 2000 childhood cancer survivors who previously received potentially nefrotoxic treatment will be asked to participate in the DCOG-LATER Q2008 nefrology study.

Exclusion criteria

Exclusion criteria: diagnosis of childhood cancer with survival less than 5 years, age at diagnosis >18 years or diagnosed while residing in foreign country, no nefrotoxic treatment

Design outcomes

Primary

MeasureTime frame
1) Prevalence of glomerular dysfunction in 5-year survivors of childhood cancer treated with possible nefrotoxic modalities (comparisons: high risk versus low-risk group; high-risk group versus reference values from general population; low riskgroup versus reference values general population) 2) Prevalence of tubular dysfunction in 5 year CCS treated with potential nefrotoxic therapy (comparisons: high risk versus low-risk group; high-risk group versus reference values from general population; low riskgroup versus reference values general population) 3) Treatment related-risk factors for abnormal diagnostic renal fucntion tests 4) Hypertension (in relation to glomerular function) 5) Diagnostic value of Cystatin C voor glomerular dysfunctie

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)