Objectives
We sought to determine the clinical performance of visual inspection with acetic acid (VIA), digital cervicography (DC), Xpert HPV, and OncoE6 for cervical cancer screening in an HIV-infected population.
Methods
HIV-infected women 18 years and older were included in this cross-sectional validation study conducted in Lusaka, Zambia. The screening tests were compared to a histological gold standard. We calculated sensitivity, specificity, positive and negative predictive values, positive and negative likelihood ratios, and odds ratios using cervical intra-epithelial neoplasia grade 2 or worse (CIN2+) and grade 3 or worse (CIN3+) thresholds.
Results
Between January and June 2015, 200 women were enrolled. 15% were screen positive by VIA, 20% by DC, 47% by Xpert HPV, and 6% by OncoE6. Using a CIN2+ threshold, the sensitivity and specificity of VIA was 48% (95% confidence interval [CI]: 30-67%) and 92% (95% CI: 86-95%), respectively. Similarly, the sensitivity and specificity of DC was 59% (95% CI: 41-76%) and 88% (95% CI: 82-93%). The sensitivity and specificity of Xpert HPV was 88% (95% CI: 71-97%), and 60% (95% CI: 52-68%). Finally, the sensitivity and specificity of OncoE6 was 31% (95% CI: 16-50%) and 99% (95% CI: 97-100%).
Conclusions
VIA and DC displayed moderate sensitivity and high specificity. Xpert HPV performed equivalently to currently approved HPV DNA tests, with high sensitivity and moderate specificity. OncoE6 displayed excellent specificity but low sensitivity. These results confirm an important role for VIA, DC, and Xpert HPV in screen-and-treat cervical cancer prevention in low- and middle-income countries, such as Zambia.