Hearing Loss and Complaint in Patients With Head and Neck Cancer Treated With Radiotherapy

Sponsor
Hospital A.C. Camargo (Other)
Overall Status
Completed
CT.gov ID
NCT01102621
Collaborator
(none)
282
1
29.9
9.4

Study Details

Study Description

Brief Summary

Hypothesis: Treatment for head and neck tumors often involve methods that affect the auditory system and cause hearing loss. Neck dissection negatively impacts the lymphatic drainage, chemotherapy uses ototoxic drugs, radiotherapy affects blood flow and tissue radiation is toxic to the ear and may lead to hearing losses of various types and degrees.

Objective: To investigate occurrences of hearing loss and complaints among patients with head and neck tumors who underwent radiotherapy.

Study design: Prospective, case-control study. Setting: Tertiary care center hospital.

Subjects and Methods: 282 subjects were evaluated, 141 with head and neck tumors and 141 as an age-matched control group. The controls had never undergone oncological treatment that put their hearing at risk. All subjects underwent audiological evaluation, including the HHIE questionnaire, pure tone audiometry, speech audiometry and immittance audiometry. The radiation dose received by the auditory system was calculated based on the percentage of the external auditory canal included in the radiation field.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    282 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Hearing Loss and Complaint in Patients With Head and Neck Cancer Treated With Radiotherapy
    Study Start Date :
    Jan 1, 2005
    Actual Primary Completion Date :
    Jan 1, 2007
    Actual Study Completion Date :
    Jul 1, 2007

    Arms and Interventions

    Arm Intervention/Treatment
    case-control, head and neck cancer with radiotherapy

    The group of exposed individuals had to be patients with disease-free survival interval of at least two years subsequent to treatment for head and neck cancer by means of radiotherapy alone or in combination, in which the auditory system was included in the field of irradiation.

    case-control, head an neck cancer without radiotherapy

    The group of non-exposed individuals (control group) had to be patients who had not undergone oncological treatment that put their hearing at risk and who were age-matched (2 years). This group was formed by individuals who had had pelvic tumors or skin tumors and who had only undergone local surgery to remove their tumors, and by female volunteers from the hospital. All of these individuals were asked whether they would be willing to participate in a study, without knowing in advance whether they had any previous hearing problems or complaints.

    Outcome Measures

    Primary Outcome Measures

    1. The hearing loss was evaluated through conventional tone threshold audiometry and a questionaire of hearing handicap was applied to both groups (individuals exposed to radiotherapy and the control group). [patientes were evaluated two years after finished the treatement]

      We observed mild to moderate hearing losses at frequencies of 57.4% in right ears and 59.6% in left ears in the group exposed to radiotherapy and in the control group, 43.3% ofmild to moderate hearing loss in both ears.Severe or profound hearing losses or anacusis occurred at frequencies of 6.4% in right ears and 8.5% in left ears, versus only 1.4% in the control group.Furthermore, severe handicap was observed in 2.8% of the individuals in the control group, versus 19.1% in the group exposed to radiotherapy.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    11 Years to 84 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • The group of exposed individuals

    • had to be patients with disease-free survival interval of at least two years subsequent to treatment for head and neck cancer

    • radiotherapy alone or in combination, in which the auditory system was included in the field of irradiation.

    • The group of non-exposed individuals (control group)

    • had to be patients who had not undergone oncological treatment that put their hearing at risk

    • age-matched (2 years). This group was formed by individuals who had had pelvic tumors or skin tumors and who had only undergone local surgery to remove their tumors, and by female volunteers from the hospital.

    • All of these individuals were asked whether they would be willing to participate in a study, without knowing in advance whether they had any previous hearing problems or complaints.

    Exclusion Criteria:
    • congenital hearing loss

    • otological surgery

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital A C Camargo São Paulo SP Brazil 01509-900

    Sponsors and Collaborators

    • Hospital A.C. Camargo

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01102621
    Other Study ID Numbers:
    • HL1
    First Posted:
    Apr 13, 2010
    Last Update Posted:
    Apr 13, 2010
    Last Verified:
    Mar 1, 2010

    Study Results

    No Results Posted as of Apr 13, 2010