WES of NF2-associated in Comparison to Sporadic Vestibular Schwannomas - Correlation With Clinical Data
- Conditions
- Acoustic NeuromaNeurofibromatosis Type 2Vestibular Schwannoma
- Interventions
- Diagnostic Test: Whole exome sequencing
- Registration Number
- NCT03210285
- Lead Sponsor
- University Hospital Tuebingen
- Brief Summary
Whole exome sequencing (WES) of 50 sporadic and 50 Neurofibromatosis Type2 (NF2)-associated vestibularis schwannomas (VS) in children and young adults. The aim is to gain insight into the complete genome of the NF2 associated VS compared to sporadic VS (control group). These data are to be correlated with the clinic, ie the auditory function (audiogram, acoustically evoked potentials) and the clinical picture as well as the tumor growth rate and general data such as sex, age, side, etc.
- Detailed Description
Whole exome sequencing (WES) of 50 sporadic and 50 Neurofibromatosis Type2 (NF2)-associated vestibularis schwannomas (VS) in children and young adults. The aim is to gain insight into the complete genome of the NF2 associated VS compared to sporadic VS (control group). These data are to be correlated with the clinic, ie the auditory function (audiogram, acoustically evoked potentials) and the clinical picture as well as the tumor growth rate and general data such as sex, age, side, etc.
The analysis of genetic changes should provide a better insight into the oncogenesis of these tumors. The distinct genetic characteristics between NF2-associated and sporadic VS suggest a different oncogenesis of these tumors.
The correlation of the genetic characteristics with the partly very different clinical appearance and a very different dynamics of the disease, in particular the tumor volume in the course, identifies the underlying modifiers of the disease course.
Based on these genetic modifiers, patients can be stratified and individual clinical therapy decisions can be made.
By demonstrating these genetic profiles in the peripheral blood, prospective conclusions can be drawn about expected disease progression before intervention as well as for therapy monitoring
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 70
- Study population: Operated NF2-associated VS
- Control group: Operated sporadic VS
- Consent to participation in the study by the patient / legal guardian in prospective inclusion or consent to the use of stored specimens in retrospective inclusion
- Age: 0 -99 years
- Lack of informed consent
- Patient's request (withdrawal of the consent statement for the evaluation of the data and further storage of the blood / tissue samples)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description NF2-associated VS Whole exome sequencing Patients after surgery of a NF2- associated vestibularis schwannoma: Whole exome sequencing of blood and tumor tissue Sporadic VS Whole exome sequencing Patients after surgery of a sporadic vestibularis schwannoma: : Whole exome sequencing of blood and tumor tissue
- Primary Outcome Measures
Name Time Method Correlation clinical-volumetric pathologies and distinct genetic features Within 1 week after measurement Correlation between interindividually different clinical-volumetric pathologies and distinct genetic features
- Secondary Outcome Measures
Name Time Method Identification of genetic profiles for pre-interventional prediction of expected disease progression Within 1 week after measurement Identification of genetic profiles in the peripheral blood for pre-interventional prediction of expected disease progression as well as therapy monitoring
Trial Locations
- Locations (1)
University Department of Neurosurgery Tübingen
🇩🇪Tübingen, Germany