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Assessment of Endocrine and Metabolic Late Effects After Childhood Brain Tumor Treatment

Late Endocrine and Metabolic Consequences of Treatment of Primary Brain Tumors in Childhood

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07716579
Enrollment
12
Registered
2026-07-21
Start date
2023-07-03
Completion date
2025-12-31
Last updated
2026-08-13

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

Conditions

Brain Neoplasms, Endocrine System Diseases, Metabolic Diseases

Keywords

Childhood Brain Tumor Survivors, Late Effects of Cancer Treatment, Endocrine Late Effects

Brief summary

This prospective, single-group interventional study evaluates endocrine and metabolic late effects in survivors of primary brain tumors treated during childhood. According to the study protocol, participants were prospectively assigned to undergo the Study-Specific Endocrine and Metabolic Late-Effects Assessment. The assessment included anthropometric measurements, repeated blood pressure measurements, clinical endocrine evaluation, fasting laboratory testing, and protocol-defined bone and vascular assessments. The purpose of the study was to identify the frequency and severity of endocrine and metabolic late effects and to evaluate their associations with tumor characteristics, previous cancer treatment, age at diagnosis, and physical functioning.

Detailed description

Survivors of primary brain tumors treated during childhood may develop endocrine, metabolic, neurological, psychological, and cardiovascular late effects several years after completion of cancer treatment. This prospective, single-group interventional study included individuals who had been treated for a primary brain tumor in Slovenia between 2008 and 2018 while aged 0 to 18 years and who had survived for at least 5 years after diagnosis. Following enrollment and informed consent, all participants were prospectively assigned, according to the study protocol, to undergo the same Study-Specific Endocrine and Metabolic Late-Effects Assessment. Participation in the study determined the standardized manner and intensity with which the protocol-defined procedures were performed; participants would not otherwise necessarily have received the same assessment package during routine clinical follow-up. The protocol-defined assessment included review of medical history and previous cancer treatment, measurement of body weight, height, waist and hip circumference, arm span and sitting height, repeated blood pressure measurements, clinical assessment of endocrine and pubertal status, and fasting laboratory testing of endocrine and metabolic markers. The study-specific assessment also included vascular evaluation by measurement of carotid intima-media thickness.When the relevant results were not already available, dual-energy X-ray absorptiometry for the assessment of bone mineral density and body composition, and pulse wave velocity assessment, were performed or arranged according to the study protocol. Medical record data on tumor type and location, age at diagnosis, treatment modalities, date of treatment completion, current therapy, and previously identified late effects were also collected. No investigational medicinal product was administered. The primary objective was to identify the occurrence and severity of endocrine and metabolic late effects following treatment of childhood brain tumors. Additional analyses evaluated associations between the identified late effects and tumor location, tumor type, treatment modality, age at diagnosis, and physical functioning.

Interventions

OTHERStudy-Specific Endocrine and Metabolic Late-Effects Assessment

According to the study protocol, participants underwent a study-specific assessment to identify endocrine and metabolic late effects after treatment of a primary brain tumor during childhood. The assessment included anthropometric measurements, repeated blood pressure measurements, clinical assessment of endocrine and pubertal status, and fasting laboratory testing of endocrine and metabolic markers. Vascular assessment included measurement of carotid intima-media thickness. Bone mineral density, body composition, and pulse wave velocity assessments were performed or arranged according to the protocol when the relevant results were not already available.

Sponsors

Institute of Oncology Ljubljana
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

All participants were prospectively assigned to one protocol-defined study intervention: a study-specific endocrine and metabolic late-effects assessment. The same assessment strategy was used for all participants. There was no comparator group and no randomization.

Eligibility

Sex/Gender
ALL
Age
5 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Individuals treated for a primary brain tumor in Slovenia between 2008 and 2018 while aged 0 to 18 years. * Survival for at least 5 years after the diagnosis of a primary brain tumor. * Written informed consent provided by the participant or, when applicable, by a parent or legal guardian.

Exclusion criteria

* Failure to meet the inclusion criteria. * Absence of written informed consent from the participant or, when applicable, from a parent or legal guardian.

Design outcomes

Primary

MeasureTime frameDescription
Number and Percentage of Participants With at Least One Endocrine or Metabolic Late EffectBaselineNumber and percentage of participants with at least one endocrine or metabolic late effect identified by the protocol-defined Study-Specific Endocrine and Metabolic Late-Effects Assessment. Late effects were identified using medical history, clinical endocrine evaluation, anthropometric measurements, repeated blood pressure measurements, and laboratory findings, including growth-related, thyroid, gonadal, adrenal, glucose, insulin, lipid, liver, and vitamin D parameters.

Secondary

MeasureTime frameDescription
Number and Percentage of Participants With Endocrine or Metabolic Late Effects by Tumor and Treatment CharacteristicsBaselineNumber and percentage of participants with endocrine or metabolic late effects, summarized according to tumor type and location, age at diagnosis, and previous treatment characteristics, including surgery, chemotherapy, and radiotherapy.

Countries

Slovenia

Contacts

PRINCIPAL_INVESTIGATORLorna Zadravec Zaletel, MD, PhD

Institute of Oncology Ljubljana

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026