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Ototoxicity, Drug-InducedBIO-OTOTOXNCT06490029

Diagnostic of Various Ototoxicity Induced by Cancer Treatment

An observational study of Ototoxicity, Drug-Induced, run by Direction Centrale du Service de Santé des Armées at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Visit the clinic once every 2 weeks for checkups and tests The goal of this clinical trial is to learn if systematic hearing tests (eg fonctional assesment, electrophysiology and seric biomarkers) can diagnose hidden hearing loss or vestibular troubles in a population of patients treated for cancer; population study… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Ototoxicity, Drug-Induced
What is being tested?
Auditory, vestibular and electrophysiological investigations and Biologic investigations; seric proteins
How many people
540 participants
Where
1 siteFrance
Study dates
19 Jun 2024to 19 Sep 2027
How long will I take part?
39 Months
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: patients treated, not treated or to be treated for cancer or hematologic recquiring neurotoxic treatment

Who may be able to join

  • Age 18 and over
  • Registered with social security
  • Signed consents
  • Absence of presbycusis prior to cancer treatment (groups A and C)
  • No known presbycusis (group B)
  • Previous exposure to an ototoxic/neurotoxic agent (group A)
  • Indication for initiation of ototoxic/neurotoxic therapy (group C)

Who cannot join

  • - Subjects deprived of liberty
  • Subjects unable to read or write the French language
  • Pregnant and breast-feeding women
  • Previous treatment for ototoxicity
  • History of bilateral auditory pathology, in particular otosclerosis, perilymphatic fistula, ruptured tympanic membrane, autoimmune hearing loss, acoustic neuroma.
  • History of severe head trauma (Glasgow Coma Score <= 8)
Show all 10Show fewer
  • Abnormal otoscopy or tympanometry In addition for group B
  • Previous chemotherapy
  • Previous ENT radiotherapy
  • Ongoing ototoxic drug therapy (quinine, diuretics, aminoglycosides, aspirin, NSAIDs) or corticosteroid therapy

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

François-Régis FERRAND contact

0178651249

francois-regis.ferrand@def.gouv.fr

France1 site, 1 recruiting
  • HIA Bégin

    Paris

    Recruiting

Other trials in France

About this study

Official title: Evaluation of Hidden Hearing Loss and Vestibular Damage Induced by Anti-cancer Treatments

  • Visit the clinic once every 2 weeks for checkups and tests The goal of this clinical trial is to learn if systematic hearing tests (eg fonctional assesment, electrophysiology and seric biomarkers) can diagnose hidden hearing loss or vestibular troubles in a population of patients treated for cancer; population study will include different population in terms of sex/gender, age, medical condition (cancer patients treated with surgery alone and/or radiotherapy and/or chemotherapy, and healthy volunteers).

The main question it aims to answer is:

Read more
  • To assess the ototoxicity of anticancer drugs using a combination of auditory functional tests (including speech audiometry in noise), vestibular test , plasmatic samples and electrophysiological measures.

Participants will be studied:

Either only after exposition (single visit) Or before, during and after the exposition to potential otototoxic agents with a 4 times Visit the clinic checkups and tests (one before, two while ongoing potential ototoxic agents and 1 post exposition)

Participants will complete questionnaires, undergo audiometric and electrophysiological tests, and their routine biomedical data will be studied, without any modification of the routine care (planned cancer treatment)

Read the detailed description

Ototoxicity refers to all the auditory and vestibular consequences of a mechanical, radiological and/or chemical aggressor, which can affect these functions via common or specific mechanisms.

Quantification of auditory damage (whatever the type of aggressor) is currently mainly assessed by pure tone audiometry (TTA). However, apart from its subjectivity, LTA only takes into account the audibility of auditory signals - most often only the frequencies of the speech spectrum - and not an individual's ability to analyze and interpret these signals. From an objective point of view, apart from acoustic otoemissions, which have revolutionized neonatal hypoacusis screening, ototoxicity assessment suffers from the absence of reliable biomarkers, objective witnesses of a lesion more or less specific to the type of aggression.

Patients undergoing treatment for cancer are exposed to numerous iatrogenic risks that potentially impact quality of life, whether in a curative or palliative context. In terms of ototoxicity to anticancer drugs (mainly platinum salts), less than half of patients benefit from follow-up during and after exposure to these treatments, despite existing recommendations for cisplatin. There are no recommendations for other anti-cancer drugs (including other platinum salts and neurotoxic drugs) in the absence of clear evidence of a reduction in ATL scores, but the analysis of the literature shows above all a lack of screening for other forms of ototoxicity. Yet the potential consequences of failing to treat hypoacusis can be dramatic: a strong statistical link has been demonstrated, notably with the risk of dementia and mortality, which could also be impacted by the increased risk of falls caused by impaired balance due to vestibulotoxicity (the investigation of which is exceptional in the absence of a vertigo attack).

Areas for improvement include prevention recommendations, improved accessibility to audiometric monitoring, and the development of robust, time-saving diagnostic tests (in patients who often present with other iatrogenic or cancer-induced problems) - the main focus of our study - and the identification of effective treatments.

Vocal noise audiometry (VNA) is an ideal candidate for describing hearing impairment in cancer patients, because :

  • Difficulty understanding speech in noise is one of the first signs of hearing loss in the case of peripheral disorders such as presbycusis (linked to ageing) or central auditory disorders, making it possible to account for ototoxicity linked to different mechanisms or damage to different compartments of the auditory system.
  • AVB allows assessment under more ecological conditions, i.e., closer to situations encountered in everyday life, than those of tone or voice audiometry in silence, and in a less restrictive way (in terms of time taken to perform the test, and not requiring access to an audiometric booth).

However, the various reference techniques used to assess AVB differ in complexity (comprehension of sentences, syllables, dissyllabic words or logatomes), normative value, conditions and duration, making analysis of intelligibility functions all the more complex. It is generally accepted that logatomes enable us to test the periphery of the auditory system, whereas words and sentences involve mental substitution and the subject's semantic knowledge, and therefore enable us to test hearing in conditions closer to those encountered in everyday life.

In a population particularly exposed to the risk of fatigue and cognitive disorders (chemo-induced cognitive disorders), it is therefore necessary to carry out a study incorporating quality of life questionnaires to take these associated factors into account. In addition, depending on the treatment (and its intensity) and cancer location, different compartments of the auditory system may be affected by the risk of ototoxicity, requiring objective tests (at least on part of our study population) to assess the vestibule, inner ear - in particular to differentiate ciliopathy from cochlear synaptopathy - and middle ear, in order to clarify their respective involvement in functional loss.

The investigators propose to study these parameters in several patient populations, exposed - or not - to ototoxic and/or neurotoxic agents. Comparison within and between these different populations will enable us to assess the specificity and sensitivity of the subjective and objective tests proposed in this study, as well as the validity of composite biomarkers constructed from results on specific groups.

Being tested
Auditory, vestibular and electrophysiological investigations, Biologic investigations; seric proteins
Medical subject headings
Ototoxicity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Auditory, vestibular and electrophysiological investigationsDiagnostic test

    otoacoustic emissions, electrocochleography, vocal audiometry in noise and high-frequency tonal audiometry, impedancemetry

  • Biologic investigations; seric proteinsDiagnostic test

    seric proteins

Study groups in NCT06490029
Study groupRoleWhat they receive
A:Previously exposed to CISPLATIN with significant ATL damageGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to CISPLATIN without significant ATL damageGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to cochlear RADIOTHERAPY with significant ATL damageGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to cochlear RADIOTHERAPY WITHOUT significant ATL damageGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to cochlear RADIOTHERAPY & CISPLATIN with significant ATL damageGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to cochlear RADIOTHERAPY & CISPLATIN WITHOUT significant ATL damageGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to OXALIPLATINGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to CARBOPLATINGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to TAXANESGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to VINCALCALOIDSGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Previously exposed to other neurotoxicantGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
B:Patients cured of cancer without ototoxic or neurotoxic exposureGroupe B
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
B:Companions without ototoxic or neurotoxic exposureGroupe B
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Hyperacusic patients following cancer treatmentGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Tinnitus patients following cancer treatmentGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
A:Patients with vestibular disorders following cancer treatmentGroupe A
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations
C:Patients with an indication for CISPLATIN recruited prior to any treatmentGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins
C:Patients indicated for cochlear radiotherapy and recruited prior to treatmenGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins
C:Patients with indication for CISPLATIN and cochlear radiotherapy recruited prior any treatmentGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins
C:Patients with an indication for OXALIPLATIN treatment recruited prior to any treatmentGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins
C:Patients with indication for CARBOPLATIN recruited prior to any treatmentGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins
C:Patients with indication for TAXANES therapy recruited prior to any treatmentGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins
C:Patients with indication for VINCALCALOIDES or other neurotoxicantGroupe C
Receives: Diagnostic Test: Auditory, vestibular and electrophysiological investigations; Diagnostic Test: Biologic investigations; seric proteins

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Descriptive statistics for audiometry of the various groups

    Percentage of correct consonant identification as a function of signal-to-noise ratio for speech audiometry in noise

    Measured: Day 0-Day1 (groups A, B, C) & Day 2, Day 0+7-14-21, Day 0+180-270 (for group C)

  2. Descriptive statistics for electrophysiological tests of the various groups

    amplitudes of the acoustic distortion products collected during the measurement of induced acoustic otoemissions

    Measured: Day 0-Day1 (groups A, B, C) & Day 2, Day 0+7-14-21, Day 0+180-270 (for group C)

  3. Descriptive statistics for protein analyses of the various groups

    Concentration of selected proteins in plasma (/mL)

    Measured: Day 0-Day1 (groups A, B, C) & Day 2, Day 0+7-14-21, Day 0+180-270 (for group C)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Jul 2024
  2. Study start19 Jun 2024
  3. Primary completion19 Mar 2025 (estimated)
  4. Study completion19 Sep 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
540 participants (estimated)
Target duration
39 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06490029
Sponsor's protocol ID
2023RC04
Acronym
BIO-OTOTOX
Status last verified
Jun 2024
First submitted
19 Jun 2024
Last updated
8 Jul 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Ototoxicity, Drug-Induced, run by Direction Centrale du Service de Santé des Armées at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 8 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact François-Régis FERRAND (0178651249, francois-regis.ferrand@def.gouv.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Descriptive statistics for audiometry of the various groups (time frame: Day 0-Day1 (groups A, B, C) & Day 2, Day 0+7-14-21, Day 0+180-270 (for group C)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jul 2024.

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