Screening Study for Cervical Pre-cancer and Cancer Prevention in South African Women.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age25-75
SponsorUniversity of Pretoria

About this trial

Nearly 8 000 new cervical cancer cases are diagnosed in South Africa per year; many are still undiagnosed and about 50% of diagnosed cases succumb per year. Although the current prevalence of pre-cancer cervical disease is largely unknown, data from local studies suggest regional differences and an increase in the prevalence of cytological abnormalities when compared with historical data. Low frequency in cytology screening is the primary factor attributable to development of invasive cervical cancer and almost one-third of all cervical cancer patients had previous negative cytology. Due to the low sensitivity of cytology it can be assumed that the true prevalence of pre-cancer disease is underestimated by all available data. One round of optimal cervical cytology will detect around 50% of existing pre-cancer cervical disease as identified and proven using colposcopy and directed biopsy. It is now widely accepted that primary screening with a human papilloma virus (HPV) test can improve the sensitivity of screening and that even a single round of HPV screening can rapidly reduce the incidence of invasive cervical cancer and related mortality within a few years.

South Africa has a high prevalence of HIV infection and a delay in or failure to initiate antiretroviral therapy (ART). These facts, together with the largely unscreened status of the female population and the high incidence of cervical cancer all suggest that HPV infection and precursors to cervical cancer are both unusually common among South African women. Accurate current knowledge of the performance of newer generation HPV based screening tests in HIV-infected and general female population are essential for cost-analysis and planning for national prevention and screening programs. This study will aim to demonstrate the feasibility and efficacy of new generation HPV deoxyribonucleic acid (DNA) based screening assays in a South African setting.

The investigators hypothesize that HPV testing followed by normal and special cytology tests will be a successful screening model for a South African population.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Informed consent accepted and signed

Health seeking behaviour or request for a cervical cancer screening test

Willing and able to receive test result by automated text message or clinic visit

Disqualifiers

Current pregnancy

Hysterectomy

Current or previous treatment for gynaecological cancer

Hesitant or unable to undergo screening and treatment if indicated

Trial population

This is a multicentric study carried out in South Africa. Women with unknown HIV status will be recruited from the general population, and HIV positive women from adult antiretroviral treatment (ART) clinics.

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

  • Screening

    Other intervention

    Cervical specimen obtained using speculum examination and cervical collection bush.

  • Colposcopy

    Other intervention

    Vaginal speculum examination followed by application of 2% acetic acid and lugol's iodine with inspection with colposcope and punch biopsies taken of abnormal areas.

  • LLETZ

    Procedure/Surgery

    The above (see colposcopy) is followed by local anaesthetic with two dentist's ampoules of lignocaine and large loop excision using coagulation of the abnormal area (usually 2 x 3 x 1 cm).

Treatment groups

1,500 Participants
are divided into 3 treatment groups
Group A: HIV pos3 interventions
Group B: HIV neg3 interventions
Group C: HIV unk3 interventions

Trial outcomes

Primary outcomes

1

Number of women with histologically proven cervical intraepithelial neoplasia grade 2+ (CIN2+) detected using HPV DNA analysis with partial genotyping as primary screen test followed by cervical cytology and immunocytochemistry as triage tests

Time frame
Detected on histology biopsy at colposcopy after initial HPV screening with simultaneous cytology and immunocytochemistry testing

Secondary outcomes

1

Number of women with CIN2+ detected using HPV DNA analysis with partial genotyping that is associated with HPV types 16, 18, 16 and/or 18, only other high risk types

Time frame
Detected on histology biopsy at colposcopy after initial HPV screening with simultaneous cytology and immunocytochemistry testing

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Pretoria

Lead sponsor

University of Stellenbosch

Collaborator