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DOI: 10.1055/s-0044-1789274
Revolutionizing Cervical Cancer Screening: Self-Vaginal Sampling for Human Papillomavirus Detection
Abstract
Self-vaginal sampling (SVS) is a promising tool for cervical cancer prevention, offering a convenient and cost-effective alternative to traditional screening. With an 80% lifetime risk of HPV infection among women, SVS improves accessibility, particularly for marginalized communities and older women who are often excluded from routine screening. It reduces discomfort, empowers self-care, and provides insights into the vaginal microbiome, aiding in the detection of pathogens beyond HPV. However, challenges such as loss to follow-up, sampling errors, and misconceptions persist. Despite these hurdles, SVS remains a vital strategy for increasing screening participation and reducing cervical cancer disparities.
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Keywords
cancer prevention - cervical cancer screening - cost-effective - high-risk human papillomavirus - self-vaginal samplingWith an 80% lifetime risk of human papillomavirus (HPV) infection among women, and a 0.6% risk of cervical cancer, the importance of effective screening methods cannot be overstated. Self-vaginal sampling (SVS) emerges as a promising tool in the fight against HPV, offering convenience, cost-effectiveness, and the potential to delve into the intricate world of vaginal microbiota.[1] [2]
Participation in prevention programs is key to reducing the incidence and mortality from cervical cancer. SVS not only enhances accessibility to screening but also addresses barriers that hinder participation in conventional methods. Its home-based approach minimizes discomfort and empowers women to take charge of their health. Furthermore, SVS provides insights into the vaginal microbiome, aiding in the detection of pathogens beyond HPV.[3] [4]
However, challenges loom over SVS implementation. Loss to follow-up remains a concern, while issues like low self-efficacy and sampling errors pose obstacles ([Fig. 1]). Misconceptions and fear surrounding the procedure can lead to suboptimal sampling, impacting the accuracy of results. Additionally, inadequate training and communication gaps may compromise the quality of samples obtained.[5]
Despite these hurdles, SVS holds promise in narrowing health disparities, particularly in marginalized communities. Its role becomes even more pivotal in times of crises like the COVID-19 pandemic, offering a safe screening alternative. By prioritizing patient-centered care and fostering inclusivity, SVS emerges as a beacon of hope in the realm of cervical cancer screening.[4]
One of the very important aspects of SVS is that we can also include women in the age group of ≥60 years, which are always excluded from regular studies of screening program. Screening for HPV becomes increasingly vital for women in older than 60 years, given the limitations of cytology in detecting cervical abnormalities effectively. Moreover, this demographic often faces exclusion from routine screening programs, resulting in late identification of cervical cancer and its progression into more aggressive forms.


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Conflict of Interest
None declared.
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References
- 1 Bik EM, Bird SW, Bustamante JP. et al. A novel sequencing-based vaginal health assay combining self-sampling, HPV detection and genotyping, STI detection, and vaginal microbiome analysis. PLoS One 2019; 14 (05) e0215945
- 2 Latsuzbaia A, Vanden Broeck D, Van Keer S. et al. Clinical performance of the realtime high risk HPV assay on self-collected vaginal samples within the VALHUDES framework. Microbiol Spectr 2022; 10 (05) e0163122
- 3 Stanczuk G, Baxter G, Currie H. et al. Clinical validation of hrHPV testing on vaginal and urine self-samples in primary cervical screening (cross-sectional results from the Papillomavirus Dumfries and Galloway-PaVDaG study). BMJ Open 2016; 6 (04) e010660
- 4 Daponte N, Valasoulis G, Michail G. et al. HPV-based self-sampling in cervical cancer screening: an updated review of the current evidence in the literature. Cancers (Basel) 2023; 15 (06) 1669
- 5 Hariprasad R, John A, Abdulkader RS. Challenges in the implementation of human papillomavirus self-sampling for cervical cancer screening in India: a systematic review. JCO Glob Oncol 2023; 9: e2200401
Address for correspondence
Publikationsverlauf
Artikel online veröffentlicht:
22. August 2024
© 2024. MedIntel Services Pvt Ltd. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Bik EM, Bird SW, Bustamante JP. et al. A novel sequencing-based vaginal health assay combining self-sampling, HPV detection and genotyping, STI detection, and vaginal microbiome analysis. PLoS One 2019; 14 (05) e0215945
- 2 Latsuzbaia A, Vanden Broeck D, Van Keer S. et al. Clinical performance of the realtime high risk HPV assay on self-collected vaginal samples within the VALHUDES framework. Microbiol Spectr 2022; 10 (05) e0163122
- 3 Stanczuk G, Baxter G, Currie H. et al. Clinical validation of hrHPV testing on vaginal and urine self-samples in primary cervical screening (cross-sectional results from the Papillomavirus Dumfries and Galloway-PaVDaG study). BMJ Open 2016; 6 (04) e010660
- 4 Daponte N, Valasoulis G, Michail G. et al. HPV-based self-sampling in cervical cancer screening: an updated review of the current evidence in the literature. Cancers (Basel) 2023; 15 (06) 1669
- 5 Hariprasad R, John A, Abdulkader RS. Challenges in the implementation of human papillomavirus self-sampling for cervical cancer screening in India: a systematic review. JCO Glob Oncol 2023; 9: e2200401



