Cervical Cancer Screening and Treatment Algorithms Using Human Papillomavirus Testing—Lessons Learnt from a South African Pilot Randomized Controlled Trial

Author:

Sebitloane Hannah M.1ORCID,Forestier Mathilde23ORCID,Ginindza Themba G.45ORCID,Dhlomo Wendy1ORCID,Moodley-Govender Eshia1ORCID,Darragh Teresa M.6ORCID,Baena Armando2ORCID,Herrero Rolando27ORCID,Almonte Maribel238ORCID,Broutet Nathalie3ORCID,De Vuyst Hugo23ORCID

Affiliation:

1. 1Discipline of Obstetrics and Gynaecology, School of Clinical Medicine, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.

2. 2Early Detection, Prevention and Infections (EPR), International Agency for Research on Cancer, Lyon, France.

3. 3Department of Reproductive Health and Research, World Health Organization, Geneva, Switzerland.

4. 4Public Health Medicine, University of KwaZulu-Natal, Durban, South Africa.

5. 5Cancer & Infectious Diseases Epidemiology Research Unit (CIDERU), College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa.

6. 6Department of Pathology, University of California, San Francisco, California.

7. 7Agencia Costarricense de Investigaciones Biomedicas, San José, Costa Rica.

8. 8Department of Non-communicable Diseases, World Health Organization, Geneva, Switzerland.

Abstract

Abstract Background: To report quantitative and qualitative results on cervical cancer human papillomavirus (HPV)-based screening and treatment algorithms, with/out triage with visual inspection after acetic acid (VIA), followed by ablative treatment (AT). Methods: Women 30 to 54 years old from Durban, South Africa were recruited, regardless of human immunodeficiency virus (HIV) status, randomized into one of two study arms and screened for HPV. VIA triage arm: HPV-positive women were triaged using VIA, biopsied and received AT if VIA positive and eligible; no triage arm: eligible HPV-positive women received AT. Women ineligible for AT were referred to colposcopy. Women were asked about side effects immediately and 1 week after AT. Retention to screening and treatment algorithms was compared between arms. Results: A total of 350 women [275 HIV-uninfected and 75 women living with HIV, (WLWH)] were allocated to receive HPV testing with VIA triage (n = 175) or no triage (n = 175). HPV prevalence was 28% [95% confidence interval (CI) = 23–33]; WLWH: 52% (95% CI = 40–64) versus HIV-uninfected: 21% (95% CI = 17–27; P < 0.05). Among women who underwent VIA triage with histologic diagnosis, 3/17 were VIA negative with cervical intraepithelial neoplasia (CIN)2+; 14/18 were VIA positive with <CIN2. Retention to screening and treatment algorithms was high (92%). Conclusions: This pilot demonstrated the feasibility of implementing screening and treatment algorithms, including performing triage and treatment in one visit; however, VIA triage did not reduce overtreatment and missed some precancerous lesions. Impact: This study reports on implementation feasibility of two World Health Organization screening and treatment algorithms (with/out VIA triage). Although the retention to screening and treatment algorithms was high in both arms, the question of how best triaging HPV-positive women deserves further consideration, particularly for WLWH.

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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