About this trial
In patients with cancer associated with human papillomavirus (HPV), the physical effects of treatment, combined with the psychosexual impact linked to HPV status, can further impair the quality of sexual life.
However, few studies have examined the specific effect of HPV status (or knowledge of status) on the recovery/quality of sexuality following radiotherapy.
It is against this backdrop that we propose a prospective longitudinal study specifically dedicated to investigating the sexual quality of life of women with HPV-positive pelvic cancer.
This type of study will enable better quantification and description of sexual dysfunction occurring after treatment, and assessment of the impact of HPV carriage, with the future aim of guiding new prevention and management strategies.
Eligibility criteria
Qualifiers
Women aged 18 or over.
Sexually active patients, i.e. those who have been sexually active in the year prior to their cancer diagnosis.
Patients being treated at the Montpellier Cancer Institute (ICM).
Patient with pelvic squamous cell carcinoma (cervix, vagina, vulva or anus) and human papillomavirus (HPV+) infection
Disqualifiers
Patients receiving radiotherapy treatment outside the Montpellier Cancer Institute (ICM).
Patients who are unwilling or unable to complete the study questionnaires.
Patients under guardianship, curatorship or court protection,
Patients for whom regular follow-up is impossible for psychological reasons,
Trial design
Treatments tested in this trial
- Assessment of sexual quality of life
Treatment groups
Locations
Sponsors and collaborators
Institut du Cancer de Montpellier - Val d'Aurelle
Lead sponsor