Obstructive Sleep Apnea Syndrome After Oropharyngeal Cancer Treatment

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Unknown

Conditions

Oropharyngeal Cancer

Obstructive Sleep Apnea Syndrome

Treatments

Radiation: Radio- chemotherapy

Procedure: Surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT02881723

2012-A00863-40 (Other Identifier)

2012-25

Details and patient eligibility

About

The level of knowledge about the consequences of oropharyngeal cancer treatment on sleep quality remains poor. Because of a high level of risk of developing an Obstructive Sleep Apnea Syndrome (OSAS), an accurate evaluation of the prevalence, of the risk factors and of the impact on quality of life is important in order to propose preventive and therapeutic solutions to these patients.

Full description

Obstructive sleep apnea syndrome (OSAS) remains poorly documented in head and neck cancer cancer population, who have a higher risk than the general population. OSAS is a risk factor for quality of life impairment and cardiovascular morbidity and mortality.

This study proposes to carry out an OSAS prevalence study among a locally advanced head and neck cancer population, already treated and to compare the consequences of current therapeutic options in sleep quality.The primary research objective will be a prevalence determination in a locally advanced stages treated population of oropharyngeal cancer. Secondary objectives will be the comparison of the prevalence between the surgical group and the radio-chemotherapy group, the research of predictive factors of presenting an OSAS and the precision of the impact on quality of life.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient aged over 18 years old, male or female;
Patient treated for a first oropharyngeal cancer located in upper airways (velum, side walls, back wall, base of tongue, vallecules), locally advanced, rated T3 or T4, whatever the stage N and M0;
Patient who received curative treatment either surgical (excision and reconstruction free flap) with adjuvant radiotherapy or concurrent chemoradiotherapy;
Treatment completed at least 12 months prior to study entry;
Patient whose cancer disease is under control at exam time;
Subject affiliated to a social security scheme;
Subject agreeing to participate in the study and who signed the informed consent form.

Exclusion criteria

Minor patient
No affiliation to a social security scheme (beneficiary or assignee);
Patient who did not signed the informed consent form
Patient with neurological disease that can affect the upper airways function
Patient has already been treated for head and neck cancer;
Patient has a lesion classified T1 or T2 or M1;
Patient has received different treatments: surgical resection without reconstruction, only radiotherapy
Unweaned alcoholic patients