Screening approaches for cervical cancer in Mozambique in HIV positive and negative women : European Journal of Cancer Prevention

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Secondary prevention & screening

Screening approaches for cervical cancer in Mozambique in HIV positive and negative women

Sineque, Albertoa,b; Catalao, Carlosc; Ceffa, Susannad; Fonseca, Ana Mariae; Parruque, Fernandaa; Guidotti, Giovannif; Massango, Cacildaa; Carrilho, Carlag,h; Bicho, Clarai; Rangeiro, Ricardinag; Orlando, Stefanoj; Marazzi, Maria Cristinak; Lorenzoni, Cesaltinag; Ciccacci, Faustol

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European Journal of Cancer Prevention 32(5):p 431-437, September 2023. | DOI: 10.1097/CEJ.0000000000000802

Abstract

Objective 

Cervical cancer (CC) is a global health issue, in Mozambique, 5300 new cases and 3800 deaths are reported each year. The WHO recommends the introduction of HPV molecular testing for CC screening, but Mozambique uses an approach based on visual inspection with acetic acid (VIA). This study aims to evaluate the feasibility of high-risk HPV (hrHPV) testing compared to actual approaches in Mozambique.

Methods 

An observational study was carried out in the DREAM center in Zimpeto, Mozambique. Women aged 30–55 were included. HPV testing was performed with the Cobas HPV test. They were then screened with the current national recommendations based on VIA. Cryotherapy was performed on-site or referred for colposcopy if necessary.

Results 

In the period, 1207 women were enrolled, 47.8% HIV+; 124 (10.3%) VIA+, and HPV DNA test was positive in 325 (26.9%) women. HPV positivity rates were higher in HIV-infected women. In the sample, 52.8% of the 124 VIA+ women were HPV uninfected and underwent unnecessary cryotherapy or colposcopy. Meanwhile, 24.7% of the 1083 VIA− women were actually HPV infected. In comparison, a screen, triage and treat approach based on hrHPV testing would only test and treat the 325 HPV-infected women.

Conclusion 

The study found high rates of hrHPV infection, particularly in HIV-positive women, with many concurrent or multiple infections. The current screening method misses important hrHPV infections and results in many unnecessary treatments. These results support the use of HPV molecular testing as the initial screening test for CC.

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