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Recruiting NCT07417072

GenoDrugP 2025: Study on Three-dimensional Models Derived From Brain Tumors in Pediatric Patients

No phase Interventional Pediatric Brain Tumors Genomics Epigenetic

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Genomic DNA analysis of biological samples.
Who it may be relevant to
Registry conditions: Pediatric Brain Tumors, Genomics, Epigenetic. Basic parameters: 3 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Preliminary Study With Biological Samples, Single-center, Non-profit, to Identify Biological Mechanisms and Resistance to Therapies in Three-dimensional Models Derived From Brain Tumors in Pediatric Patients.

Overview

Central nervous system tumours are the most common solid tumours and the leading cause of cancer mortality in children, with high biological and prognostic heterogeneity. Despite advances in the 2021 WHO molecular classifications, treatment options remain limited and often ineffective in high-grade tumours. New third-generation sequencing technologies and three-dimensional models derived from patient tumours offer promising tools for more comprehensive genomic characterisation and preclinical evaluation of drug responses. However, the lack of integrated preclinical studies remains a limitation, necessitating coordinated projects to develop personalised therapeutic strategies. The study aims to investigate the genetic and biological characteristics of paediatric brain tumours. To this end, tumour tissue samples taken during planned surgery and peripheral blood samples will be analysed. Advanced genetic analyses will be performed on these materials to identify tumour alterations and the patient's genetic characteristics. In addition, experimental in vitro models derived from the tumour will be developed to evaluate the response to different chemotherapy drugs. The information obtained will be used to better understand the mechanisms of tumour growth and resistance and to promote the future development of more targeted and personalised therapies.

Interventions

  • Diagnostic test Genomic DNA analysis of biological samples
    Analysis of genomic DNA from tumor biopsy and blood samples

Primary outcome measures

  • Number of Single Nucleotide Variants (SNV) [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Number of copy number variations (CNVs) [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Number of triplet expansions [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Number of structural variants (SVs) [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Morphological description of three-dimensional models derived from the tumour [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Vitality of three-dimensional models derived from the tumour [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Proliferative activity of three-dimensional models derived from the tumour [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Percentage of residual cell vitality after drug treatment [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]
  • Dose-response curves for each drug tested [Time frame: At enrollment and on the date of first documented progression assessed up to 12 months]

Eligibility criteria

Inclusion criteria

  • Patients aged 3-18 years with suspected brain tumours undergoing neurosurgery
  • No previous bone marrow transplants or other haematological procedures that could potentially interfere with germline analysis.
  • Patients who have not received any systemic anticancer treatment (including chemotherapy, radiotherapy or targeted therapies) prior to enrolment surgery.
  • Signature of informed consent

Exclusion criteria

  • Subsequent histological confirmation of non-neoplastic brain pathology (e.g. malformations, inflammatory lesions, demyelinating processes).
  • Insufficient quantity or quality of tumour tissue or peripheral blood for the analyses required by the protocol.
  • Presence of serious clinical conditions, systemic infections or haemodynamic instability that contraindicate the collection of biological samples or inclusion in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

Italy · 1 center
  • Meyer Children's Hospital IRCCS — Florence

Identifiers

NCT: NCT07417072 · GenoDrugP 2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗