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The distribution of FGFR3 alterations in diffuse gliomas and their relation with patient prognosis

The distribution of FGFR3 alterations in diffuse gliomas and their relation with patient prognosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094890
Enrollment
Unknown
Registered
2024-12-30
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Diffuse glioma

Interventions

FGFR3-altered group:None
Non FGFR3-altered group:None

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. aged more than 18-year old, with any gender; 2. Newly diagnosed and recurrent glioma patients who have undergone surgical treatment at our hospital. The pathology diagnosis is confirmed as glioblastoma, high-grade glioma, diffuse glioma NOS (not otherwise specified), or diffuse glioma NEC (not elsewhere classified), with a WHO grade of 2-4; 3. Molecular pathology test results has been completed or sufficient samples stored in our hospital's biobank for molecular pathology testing; 4. Molecular pathology test results show no IDH mutations and no EGFR copy number amplification or EGFRvIII mutations; 5. Participants voluntarily cooperate with follow-up;

Exclusion criteria

Exclusion criteria: 1. Cases that have only undergone biopsy or have already received treatment with corticosteroids; 2. Cases with revised pathological diagnoses of circumscribed gliomas, glioneuronal and neuronal tumors, or ependymomas, as well as cases with indeterminate diagnoses; 3. Molecular pathology tests indicate histone H3-related gene alterations or other features of RTK signaling pathway alterations, such as NTRK, ROS1, ALK, and MET fusions. 4. Restored samples do not meet the testing requirements of this project; 5. Previous physical or mental conditions that could affect the follow-up, or concurrent other malignant tumors;

Design outcomes

Primary

MeasureTime frame
Death(2 year Overall Survival);

Secondary

MeasureTime frame
Tumor recurrence confirmed by radiology(Recurrence-free survival, RFS);

Countries

China

Contacts

Public ContactYu Shi

The First Affiliated Hospital of Army Medical University

drshiyu@126.com+86 13512350865

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026