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Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation

BACKGROUND: WHO has recommended HPV testing for cervical screening where it is practical and affordable. If used, it is important to both clarify and implement the clinical management of positive results. We estimated the performance in Lusaka, Zambia of a novel screening/triage approach combining H...

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Autores principales: Parham, Groesbeck P., Egemen, Didem, Befano, Brian, Mwanahamuntu, Mulindi H., Rodriguez, Ana Cecilia, Antani, Sameer, Chisele, Samson, Munalula, Mukatimui Kalima, Kaunga, Friday, Musonda, Francis, Malyangu, Evans, Shibemba, Aaron Lunda, de Sanjose, Silvia, Schiffman, Mark, Sahasrabuddhe, Vikrant V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580629/
https://www.ncbi.nlm.nih.gov/pubmed/37845724
http://dx.doi.org/10.1186/s13027-023-00536-5
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author Parham, Groesbeck P.
Egemen, Didem
Befano, Brian
Mwanahamuntu, Mulindi H.
Rodriguez, Ana Cecilia
Antani, Sameer
Chisele, Samson
Munalula, Mukatimui Kalima
Kaunga, Friday
Musonda, Francis
Malyangu, Evans
Shibemba, Aaron Lunda
de Sanjose, Silvia
Schiffman, Mark
Sahasrabuddhe, Vikrant V.
author_facet Parham, Groesbeck P.
Egemen, Didem
Befano, Brian
Mwanahamuntu, Mulindi H.
Rodriguez, Ana Cecilia
Antani, Sameer
Chisele, Samson
Munalula, Mukatimui Kalima
Kaunga, Friday
Musonda, Francis
Malyangu, Evans
Shibemba, Aaron Lunda
de Sanjose, Silvia
Schiffman, Mark
Sahasrabuddhe, Vikrant V.
author_sort Parham, Groesbeck P.
collection PubMed
description BACKGROUND: WHO has recommended HPV testing for cervical screening where it is practical and affordable. If used, it is important to both clarify and implement the clinical management of positive results. We estimated the performance in Lusaka, Zambia of a novel screening/triage approach combining HPV typing with visual assessment assisted by a deep-learning approach called automated visual evaluation (AVE). METHODS: In this well-established cervical cancer screening program nested inside public sector primary care health facilities, experienced nurses examined women with high-quality digital cameras; the magnified illuminated images permit inspection of the surface morphology of the cervix and expert telemedicine quality assurance. Emphasizing sensitive criteria to avoid missing precancer/cancer, ~ 25% of women screen positive, reflecting partly the high HIV prevalence. Visual screen-positive women are treated in the same visit by trained nurses using either ablation (~ 60%) or LLETZ excision, or referred for LLETZ or more extensive surgery as needed. We added research elements (which did not influence clinical care) including collection of HPV specimens for testing and typing with BD Onclarity™ with a five channel output (HPV16, HPV18/45, HPV31/33/52/58, HPV35/39/51/56/59/66/68, human DNA control), and collection of triplicate cervical images with a Samsung Galaxy J8 smartphone camera™ that were analyzed using AVE, an AI-based algorithm pre-trained on a large NCI cervical image archive. The four HPV groups and three AVE classes were crossed to create a 12-level risk scale, ranking participants in order of predicted risk of precancer. We evaluated the risk scale and assessed how well it predicted the observed diagnosis of precancer/cancer. RESULTS: HPV type, AVE classification, and the 12-level risk scale all were strongly associated with degree of histologic outcome. The AVE classification showed good reproducibility between replicates, and added finer predictive accuracy to each HPV type group. Women living with HIV had higher prevalence of precancer/cancer; the HPV-AVE risk categories strongly predicted diagnostic findings in these women as well. CONCLUSIONS: These results support the theoretical efficacy of HPV-AVE-based risk estimation for cervical screening. If HPV testing can be made affordable, cost-effective and point of care, this risk-based approach could be one management option for HPV-positive women. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13027-023-00536-5.
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spelling pubmed-105806292023-10-18 Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation Parham, Groesbeck P. Egemen, Didem Befano, Brian Mwanahamuntu, Mulindi H. Rodriguez, Ana Cecilia Antani, Sameer Chisele, Samson Munalula, Mukatimui Kalima Kaunga, Friday Musonda, Francis Malyangu, Evans Shibemba, Aaron Lunda de Sanjose, Silvia Schiffman, Mark Sahasrabuddhe, Vikrant V. Infect Agent Cancer Research BACKGROUND: WHO has recommended HPV testing for cervical screening where it is practical and affordable. If used, it is important to both clarify and implement the clinical management of positive results. We estimated the performance in Lusaka, Zambia of a novel screening/triage approach combining HPV typing with visual assessment assisted by a deep-learning approach called automated visual evaluation (AVE). METHODS: In this well-established cervical cancer screening program nested inside public sector primary care health facilities, experienced nurses examined women with high-quality digital cameras; the magnified illuminated images permit inspection of the surface morphology of the cervix and expert telemedicine quality assurance. Emphasizing sensitive criteria to avoid missing precancer/cancer, ~ 25% of women screen positive, reflecting partly the high HIV prevalence. Visual screen-positive women are treated in the same visit by trained nurses using either ablation (~ 60%) or LLETZ excision, or referred for LLETZ or more extensive surgery as needed. We added research elements (which did not influence clinical care) including collection of HPV specimens for testing and typing with BD Onclarity™ with a five channel output (HPV16, HPV18/45, HPV31/33/52/58, HPV35/39/51/56/59/66/68, human DNA control), and collection of triplicate cervical images with a Samsung Galaxy J8 smartphone camera™ that were analyzed using AVE, an AI-based algorithm pre-trained on a large NCI cervical image archive. The four HPV groups and three AVE classes were crossed to create a 12-level risk scale, ranking participants in order of predicted risk of precancer. We evaluated the risk scale and assessed how well it predicted the observed diagnosis of precancer/cancer. RESULTS: HPV type, AVE classification, and the 12-level risk scale all were strongly associated with degree of histologic outcome. The AVE classification showed good reproducibility between replicates, and added finer predictive accuracy to each HPV type group. Women living with HIV had higher prevalence of precancer/cancer; the HPV-AVE risk categories strongly predicted diagnostic findings in these women as well. CONCLUSIONS: These results support the theoretical efficacy of HPV-AVE-based risk estimation for cervical screening. If HPV testing can be made affordable, cost-effective and point of care, this risk-based approach could be one management option for HPV-positive women. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13027-023-00536-5. BioMed Central 2023-10-16 /pmc/articles/PMC10580629/ /pubmed/37845724 http://dx.doi.org/10.1186/s13027-023-00536-5 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Parham, Groesbeck P.
Egemen, Didem
Befano, Brian
Mwanahamuntu, Mulindi H.
Rodriguez, Ana Cecilia
Antani, Sameer
Chisele, Samson
Munalula, Mukatimui Kalima
Kaunga, Friday
Musonda, Francis
Malyangu, Evans
Shibemba, Aaron Lunda
de Sanjose, Silvia
Schiffman, Mark
Sahasrabuddhe, Vikrant V.
Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation
title Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation
title_full Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation
title_fullStr Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation
title_full_unstemmed Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation
title_short Validation in Zambia of a cervical screening strategy including HPV genotyping and artificial intelligence (AI)-based automated visual evaluation
title_sort validation in zambia of a cervical screening strategy including hpv genotyping and artificial intelligence (ai)-based automated visual evaluation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580629/
https://www.ncbi.nlm.nih.gov/pubmed/37845724
http://dx.doi.org/10.1186/s13027-023-00536-5
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