Ototoxicity, Vestibular Schwannoma
Conditions
Keywords
Radiosurgery, Ototoxicity, Vestibular Schwannoma, Hearing loss, Quality of Life
Brief summary
The investigators aim to study the impact of stereotactic radiosurgery, for the treatment of vestibular Schwannoma, on the cochlear, vestibular, gustatory, and facial nerve functions and compare it with a conservatively treated group. The predictive value of radiological tumor characteristics on hearing preservation and vestibular function will be also evaluated. Additionally, the investigators will invite patients with vestibular Schwannoma to fill out questionnaires to assess their quality of life.
Detailed description
The study will have a retrospective part and a prospective part. The retrospective study will be based on a series of consecutive patients with vestibular Schwannoma (VS) treated either with stereotactic radiosurgery (SRS) or followed up radiologically between 2014 and 2021 in our institution. The following data will be retrieved from the hospital archiving system and will be subsequently analyzed: demographics, patient characteristics, details regarding SRS planning, clinical baseline and follow-up data, hearing, vestibular and taste function assessment initially and during follow-up, presence of additional symptoms (tinnitus, hemifacial spasm, trigeminal neuralgia), radiosurgery parameters and MRI characteristics of tumors. The following parameters will be retrospectively measured on MRI images by an experienced radiologist in each VS: tumor volume, ratio of brain stem compression, tumor shape and distance to the fundus of the internal auditory canal, length of the tumor in the internal auditory canal, and signal intensity in the cochlea and vestibule. The MRI textural features extracted from whole tumor segmentation of VSs will be calculated and analyzed with MatLab®. They include shape features, first order and second order textural features. The prospective study part aims to obtain more precise and predefined follow-up data from patients treated either with SRS or followed up conservatively from now on. Our institution's multidisciplinary skull base tumor board will be responsible for treatment decisions independently of the study. It will be a single-center observational cohort study investigating the respective impact of tumor morphology and SRS on the inner ear, the facial nerve function, and the quality of life of these patients. As data collection will be done prospectively, MRI acquisition parameters will be standardized, as well as quantification of hearing, vestibular, facial nerve function, and quality of life. Additionally, the investigators will analyze the characteristics of the tumors and several parameters of the irradiation protocol to develop predictive models for ototoxicity.
Interventions
RADIATIONStereotactic radiosurgery
Stereotactic radiosurgery
Sponsors
University Hospital, Geneva
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Aged 18 years or above * Patients with unilateral VS treated either with SRS or MRI-based observation strategy, as proposed by the institution's skull base tumor board independently of the study * Patients willing to take part in the study and give their informed consent
Exclusion criteria
* Previous surgical or radiation therapy for VS (including SRS) * Patients diagnosed with neurofibromatosis type II * Preexisting profound hearing loss, with a pure tone average (PTA) \>90 and word recognition score (WRS) \<10%, upon initial assessment * Previous middle ear surgery of the affected ear * Concurrent treatment with other experimental drugs
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of Pure Tone Average from baseline | 1-year | Hearing status as measured by audiometric tonal testing and calculated from the average of 500 Hz, 1000 Hz, 2000 Hz and 3000 Hz. |
| Change of Word recognition score from baseline | 1-year | Hearing status as measured by audiometric vocal testing and calculated as the percentage of correctly identified monosyllabic words presented at the speech recognition threshold + 40 decibel hearing level |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change of Word recognition score from baseline | 3 and 5-year | Hearing status as measured by audiometric vocal testing and calculated as the percentage of correctly identified monosyllabic words presented at the speech recognition threshold + 40 decibel hearing level |
| Change of video-oculography from the baseline | 1, 3 and 5-year | Video-oculography assessment to detect a pathologic nystagmus or a pathologic smooth pursuit |
| Change of caloric ipsilateral testing (degree of asymmetry) from baseline | 1, 3 and 5-year | Caloric testing to assess the vestibulo-ocular reflex in the low-frequency range. |
| Change of the cervical Vestibular Evoked Myogenic Potential (cVEMP) from baseline | 1, 3 and 5-year | Assessment of a present or absent reflex which reflects the function of saccule |
| Change of the ocular Vestibular Evoked Myogenic Potential (oVEMP) from baseline | 1, 3 and 5-year | Assessment of a present or absent reflex which reflects the function of utricle |
| Change of Pure Tone Average from baseline | 3 and 5-year | Hearing status as measured by audiometric tonal testing and calculated from the average of 500 Hz, 1000 Hz, 2000 Hz and 3000 Hz. |
| Change of facial nerve function from baseline | 1, 3 and 5-year | House-Brackmann scale score ranges from 1 (best) to 6 (worst) |
| Change of taste function from baseline | 6 and 12-month | Taste strips test score ranges from 0 (worst) to 16 (best) on each side of the tongue |
| Change of 36-Item Short Form Health Survey (SF-36) score from baseline | 1, 3 and 5-year | SF-36 score ranges from 0 (worst) to 100 (best) |
| Change of Penn Acoustic Neuroma Quality-of-Life (PANQOL) scale score from baseline | 1, 3 and 5-year | Penn Acoustic Neuroma Quality-of-Life (PANQOL) scale score ranges from 0 (worst) to 100 (best) |
| Change of Tinnitus Handicap Inventory (THI) score from baseline | 1, 3 and 5-year | Tinnitus Handicap Inventory (THI) score ranges from 0 (best) to 100 (worst) |
| Change of the Video Head Impulse Test (VHIT) from baseline | 1, 3 and 5-year | Assessment of the VHIT to detect dysfunction of the vestibulo-ocular reflex in the high-frequency range. |
| Change of High-frequency Pure Tone Average from baseline | 1, 3 and 5-year | Hearing status as measured by audiometric tonal testing and calculated from the average of 3000 Hz, 4000 Hz and 6000 Hz. |
Countries
Switzerland
Contacts
Primary ContactPascal Senn
Outcome results
None listed