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WES of NF2-associated in Comparison to Sporadic Vestibular Schwannomas - Correlation With Clinical Data

NCT03210285 — Completed, 70 participants, University Hospital Tuebingen

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Whole Exome Sequencing (WES) of NF2-associated in Comparison to Sporadic Vestibular Schwannomas - Correlation With Clinical Data

RegistryNCT03210285, acronym NF2
StatusCompleted
Study typeObservational
Enrollment70 (Actual)
SponsorUniversity Hospital Tuebingen (Other); collaborators: National Center for Tumor Diseases, Heidelberg
ConditionsNeurofibromatosis Type 2, Vestibular Schwannoma, Acoustic Neuroma
InterventionsWhole exome sequencing (Diagnostic test)
Datesstart 2017-07-31, primary completion 2018-04-01, completion 2018-07-01, first posted 2017-07-06, last updated 2018-07-23
Locations1 site in Germany

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-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.

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+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

+Arms and interventions

ArmTypeInterventionsDescription
NF2-associated VSDiagnostic Test: Whole exome sequencingPatients after surgery of a NF2- associated vestibularis schwannoma: Whole exome sequencing of blood and tumor tissue
Sporadic VSDiagnostic Test: Whole exome sequencingPatients after surgery of a sporadic vestibularis schwannoma: : Whole exome sequencing of blood and tumor tissue
  • Whole exome sequencing (Diagnostic test): Whole exome sequencing

+Outcome measures

Primary outcomes

  • 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 outcomes

  • 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

+Eligibility

Sex: All, ages: 1 Day to 99 Years

Inclusion Criteria:

* 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

Exclusion Criteria:

* 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)

+Locations (1)

FacilityCityCountryStatus
University Department of Neurosurgery TübingenTübingenGermany

+Investigators

My Notes