Screening for Endolymphatic Sac Tumours (ELSTs) in Von Hippel-Lindau (vHL) Patients

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Brief Title

Screening for Endolymphatic Sac Tumours (ELSTs) in Von Hippel-Lindau (vHL) Patients

Official Title

An International Collaborative Study: Screening for Endolymphatic Sac Tumours (ELSTs) in Von Hippel-Lindau (vHL) Patients

Brief Summary

      The purpose of the study is to investigate how best to screen for Endolymphatic sac tumors
      (ELSTs) in von Hippel-Lindau (vHL) patients in order to diagnose the ELSTs while they are
      still small so that hearing loss can be prevented.

      Up to 16% of vHL patients are known to develop endolymphatic sac tumors in the inner ear that
      can cause permanent hearing loss. However, the ELSTs are often not found before hearing loss
      has already occurred. The challenge for doctors is to diagnose the ELSTs at early stages
      before they cause often irreversible deafness. In order to find ELSTs before they cause
      hearing loss, it is important to screen for the tumors prophylactically, that is screen all
      vHL patients regardless of whether or not they have symptoms.

      Who can join? Persons diagnosed with vHL who are at least 15 years old. The investigators
      include patients WITH OR WITHOUT a diagnosed ELST.

      What does it involve? You need to have a hearing test and an MRI of the brain, where the
      inner ear can be seen, most vHL patients have already had this done as part of their
      surveillance program.

      Participants will be asked to participate in follow up examinations (hearing test and/or MRI
      of the brain) after 2, 5, and 10 years.

      How can I join? A doctor has to be responsible for the study in each country where vHL
      patients participates.

      Ask the doctor who manages your vHL examinations to contact us or contact us yourself and the
      investigators will help you find a doctor in your country who will participate in the study.
    

Detailed Description

      Background:

      von Hippel-Lindau disease (vHL) is a hereditary multi-system disease requiring life-long
      prophylactic surveillance. Affected individuals are predisposed to development of tumors and
      cysts in multiple organs. In recent years, it has become apparent that endolymphatic sac
      tumors (ELSTs), aggressive tumors of the petrous bone, occur in up to 16% of vHL patients.
      ELST can lead to severe and progressive hearing loss and vertigo as well as other
      audio-vestibular and neurological symptoms. However, surgical excision of tumors can preserve
      patients' pre-operative hearing level, and eliminate most other audio-vestibular symptoms. As
      even small ELSTs have been shown to lead to sudden and irreversible deafness, timely
      diagnosis of ELSTs is essential to prevent severe audio-vestibular morbidity in ELST
      patients. Several recommendations of ELST surveillance in vHL patients have been proposed;
      some suggest that diagnostic tests for ELST should be done only in vHL patients with
      subjective audio-vestibular symptoms, while others recommend audiological examinations or MRI
      of the inner ear in all vHL patients as a screening tool. However, there has not previously
      been much focus on specification of screening strategies, and it is not known, which is the
      most optimal approach. The results of a national study of ELST surveillance among Danish vHL
      patients indicated that specific patterns of audiologic parameters in patients with ELSTs,
      indicating that a distinct audiologic pattern may be typical in ELST development, perhaps
      even before the ELST is detectable on MRI. However, a larger study of audiologic parameters
      in vHL patients with and without diagnosed ELSTs is needed in order to fully investigate such
      a model and its use in early ELST detection.

      Objective The overall objective of this study is to establish audiologic characteristics
      among vHL patients with and without ELST, and investigate whether specific patterns in
      audiometric parameters correspond to different stages in ELST development.

      Material and Methods:

      The study is a multi-center prospective cohort study that includes adult vHL patients, who
      are followed with clinical interviews about subjective audio-vestibular symptoms, MRI of the
      inner ear, and audiometry.

      Results of all subjects' audiological and radiologic examinations will be collected at the
      Department of Cellular and Molecular Medicine, University of Copenhagen. Results will be
      blinded with regard to ELST history and radiologic results and evaluated by a single senior
      ear-nose-and-throat specialist, who will look for specific patterns in audiologic parameters
      over time. Radiologic images will be blinded with regard to symptoms and audiological
      examination results and will be evaluated by a single radiology specialist, who will look
      only at the inner ear and surrounding structures for presence of imaging-visible ELSTs and
      evaluate size and pattern of growth of ELSTs if possible. Audiometric characteristics will be
      correlated with presence of MRI visible ELSTs and patients' subjectively reported
      audio-vestibular symptoms to determine whether specific patterns of audiological parameters
      are distinct for ELSTs and their stages of tumor growth.

      A followed-up of all study participants is planned after 2, 5 and 10 years after patients'
      last assessed audiological examinations included in the initial study.

      The initiators of the project are responsible for evaluation and analysis of data, and are
      required to inform local project managers of any differences in their evaluation of
      examinations compared to the local evaluations of the same examinations.

      Local project managers are required to inform all of their local participants the results of
      their examinations. If any ELSTs are found in participants, local project managers must offer
      management of the ELSTs according to local recommendations. The initiators of the project
      will offer help and counseling in relation to ELST management and treatment if necessary.

      Considerations of biomedical research ethics:

      The Danish part of the study has been approved by the Danish Regional Committees on
      Biomedical Research, who have also approved that results from all participating institutions
      outside of Denmark can be collected and analyzed in Denmark. Each participating institution
      outside of Denmark must make sure that the study is also approved according to regional law.
      Oral and written consent must be obtained from all subjects, and results must be coded before
      data is sent to Denmark for analysis.

      Data management:

      The investigators have approval for the study from the Danish Data Protection Agency. All
      data analysis will take place under the University of Copenhagen in Denmark.

      Significance and perspectives:

      The present study will clarify the significance of audiologic examination in ELST
      surveillance and improve ELST screening for vHL patients.

      Publication:

      The results will be published in international, scientific journals. Collaborators will be
      included ad co-authors in any publications of the results of this study according to
      Vancouver rules.

      Funding:

      The project is financially supported as a subproject of a larger PhD project. Salary of the
      PhD student, Marie Louise Mølgaard Binderup is financed by the Danish Cancer Society with
      approximately181,000 Euros, while the expenses of operation of the PhD project is supported
      by the Lundbeck Foundation with approximately 65,000 Euros, of which approximately 4,000
      Euros is estimated to be used for expenses of the present subproject. The supporting
      organisations solely provide financial support and have no influence on study design, the
      execution of study, or publication of results. Initiators of this project will not apply for
      further financial support for this subproject.

      Collaborating institutions and participating patients will not receive any financial support
      from the mentioned sources.
    


Study Type

Observational


Primary Outcome

In each ear: development of an ELST during the study period correlated to baseline hearing level.

Secondary Outcome

 In each ear: development of an ELST during the study period correlated to hearing level at two year follow-up.

Condition

Von Hippel-Lindau Disease



Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information



Estimated Enrollment

380

Start Date

February 2011

Completion Date

December 2026

Primary Completion Date

December 2017

Eligibility Criteria

        Inclusion Criteria:

          -  A diagnosis of vHL (either a carrier of a VHL mutation or vHL diagnosed by clinical
             criteria, i.e. at least two vHL-related manifestations diagnosed or one vHL-related
             manifestation diagnosed AND a first-degree relative with vHL)

          -  At least one audiological examination (including an audiogramme) and one MRI
             examination of the brain also visualizing the inner ear within 12 months of each other

        Exclusion Criteria:

          -  Children under the age of 15 years
      

Gender

All

Ages

15 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Marie Luise Bisgaard, M.D., 004531333582, [email protected]

Location Countries

Denmark

Location Countries

Denmark

Administrative Informations


NCT ID

NCT02420067

Organization ID

H-A-2007-0125, A


Responsible Party

Sponsor-Investigator

Study Sponsor

Marie Luise Bisgaard, MD

Collaborators

 Rigshospitalet, Denmark

Study Sponsor

Marie Luise Bisgaard, M.D., Principal Investigator, Department of Cellular and Molecular Medicin, University of Copenhagen


Verification Date

May 2017