MODERN APPROACHES TO TREATMENT AND POST-TREATMENT MONITORING OF HPV-POSITIVE WOMEN WITH CERVICAL PATHOLOGY

Authors

  • Kudrat Atabayevich Jumaniyazov PhD, Associate Professor of the Department of Obstetrics and Gynecology, Urgench branch of Tashkent Medical Academy, Uzbekistan
  • Shavkat Sultanbayevich Bazarbaev Obstetrician-Gynecologist, Maternity Complex, Gurlan District Medical Association, Khorezm Region, Uzbekistan
  • Jamshid Ikromovich Reymberganov Student of the Urgench branch of Tashkent Medical Academy, Uzbekistan

DOI:

https://doi.org/10.31149/ijnps.v4i4.2860

Keywords:

Human Papillomavirus, HPV, Cervical Pathology, CIN2+, HSIL, LEEP, LLETZ, Conization, Ablation, Post-Treatment Follow-Up, hrHPV, Risk Stratification, Overtreatment, Reproductive Outcomes

Abstract

Cervical pathology in HPV-positive women remains a key problem in modern gynecology and gynecologic oncology, as it is in this group that the transition from virus carriage to clinically significant precancerous lesions and invasive cervical cancer occurs. In recent years, primary HPV screening, molecular triage, and risk stratification have significantly changed early diagnosis. However, the selection of optimal treatment strategies and the development of effective post-treatment monitoring remain the subject of active clinical debate. The main difficulty stems from the heterogeneity of the HPV-positive population: some patients have transient infection and lesions with a high probability of regression, while others develop HSIL/CIN2+ lesions, requiring timely and oncologically adequate intervention. The aim of this review article is to analyze current literature on the treatment of cervical pathology in HPV-positive women and the organization of post-treatment follow-up. This review focuses on the individualization of treatment strategies, the problem of overtreatment, the reproductive consequences of excisional procedures, the importance of follow-up hrHPV testing, and prospects for further personalization of the patient's care pathway. This paper examines current approaches to choosing between surveillance, ablative methods, LEEP/LLETZ, and conization, highlighting their advantages and limitations, and emphasizing the need to balance oncological safety with reproductive preservation. Special attention is paid to post-treatment surveillance, where follow-up hrHPV testing plays a key role as the most informative tool for the early detection of treatment failure. Factors predicting an unfavorable prognosis are discussed, including persistent hrHPV positivity, resection margin status, age, and initial lesion severity. The final section presents promising areas related to artificial intelligence, therapeutic HPV vaccines, and molecular personalization of treatment algorithms. It is concluded that treatment and follow-up of HPV-positive women should not be based on a one-size-fits-all approach, but on a step-by-step, individualized risk assessment. This allows for a simultaneous reduction in the likelihood of missing clinically significant lesions, a reduction in overtreatment, and an improvement in oncologic and reproductive outcomes.

References

[1] World Health Organization. Cervical cancer [Electronic resource]. Geneva: WHO, 2025.

[2] Bray F., Laversanne M., Sung H., et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries // CA: A Cancer Journal for Clinicians. 2024.

[3] World Health Organization. Human papillomavirus and cancer [Electronic resource]. Geneva: WHO, 2024.

[4] World Health Organization. WHO guideline for screening and treatment of cervical pre-cancer lesions for cervical cancer prevention. 2nd ed. Geneva: WHO, 2021.

[5] World Health Organization. WHO guideline for screening and treatment of cervical pre-cancer lesions for cervical cancer prevention: Use of dual-stain cytology to triage women after a positive test for human papillomavirus (HPV). 2nd ed. Geneva: WHO, 2024.

[6] Wei F., Georges D., Man I., et al. Causal attribution of human papillomavirus genotypes to invasive cervical cancer worldwide: a systematic analysis of the global literature // Lancet. 2024. Vol. 404, No. 10451. P. 435–444.

[7] Bhatla N., Aoki D., Sharma D. N., Sankaranarayanan R. Cancer of the cervix uteri: 2025 update // International Journal of Gynecology and Obstetrics. 2025. Vol. 171, Suppl. 1. P. 87–108.

[8] Clarke M. A., Wentzensen N., Perkins R. B., et al. Recommendations for use of p16/Ki67 dual stain for management of individuals testing positive for human papillomavirus // Journal of Lower Genital Tract Disease. 2024. Vol. 28, No. 2. P. 124–130.

[9] Harper D. M., Paczos T., Ridder R., Huh W. K. p16/Ki-67 dual stain triage of individuals positive for HPV to detect cervical precancerous lesions // International Journal of Cancer. 2025. Vol. 156, No. 12. P. 2257–2264.

[10] Wentzensen N., Massad L. S., Clarke M. A., et al. Self-collected vaginal specimens for HPV testing: Recommendations from the Enduring Consensus Cervical Cancer Screening and Management Guidelines Committee // Journal of Lower Genital Tract Disease. 2025. Vol. 29, No. 2. P. 144–152.

[11] Massad L. S., Clarke M. A., Perkins R. B., et al. Applying results of extended genotyping to management of positive cervicovaginal human papillomavirus test results: Enduring guidelines // Journal of Lower Genital Tract Disease. 2025. Vol. 29, No. 2. P. 134–143.

[12] Behrens A. S., Dietl A. K., Adler W., et al. Evaluation of endocervical curettage (ECC) in colposcopy for detecting cervical intraepithelial lesions // Archives of Gynecology and Obstetrics. 2024. Vol. 310, No. 6. P. 3037–3045.

[13] Bruno M. T., Cavallaro A. G., Sudano M. C., et al. Role of endocervical curettage in detecting CIN2+ in postmenopausal women with persistent high-risk HPV and type 3 transformation zone // BMC Cancer. 2025. Vol. 25. Art. 1486.

[14] Bomans L., Ramirez A. T., Hillemanns P., Gultekin M., Arbyn M. Prediction of treatment failure after excisional treatment of cervical precancer: a systematic review and meta-analysis // Obstetrics and Gynecology. 2025. Vol. 146, No. 4. P. 487–499.

[15] Bergqvist L., Virtanen A., Kalliala I., et al. Predictors for regression and progression of actively surveilled cervical intraepithelial neoplasia grade 2: a prospective cohort study // Acta Obstetricia et Gynecologica Scandinavica. 2025. Vol. 104, No. 4. P. 763–773.

[16] Lycke K. D., Kahlert J., Eriksen D. O., et al. Preterm birth following active surveillance vs loop excision for cervical intraepithelial neoplasia grade 2 // JAMA Network Open. 2024. Vol. 7, No. 3. Art. e242309.

[17] Lycke K. D., Steben M., Garland S. M., et al. An updated understanding of the natural history of cervical human papillomavirus infection: clinical implications // American Journal of Obstetrics and Gynecology. 2025.

[18] National Cancer Institute. Cervical cancer causes, risk factors, and prevention [Electronic resource]. 2024.

[19] Ye Y., Jones T., Wang T., et al. Comprehensive overview of genotype distribution and prevalence of human papillomavirus in cervical lesions // Gynecology, Obstetrics and Clinical Medicine. 2024. Vol. 4, No. 1. Art. e000005.

[20] Wang J., Zheng J., Luo X., et al. Risk factors for persistent infection of high-risk HPV in patients with cervical intraepithelial neoplasia // Cancer Management and Research. 2025.

[21] Massad L. S., et al. Colposcopy standards: guidelines for endocervical curettage at colposcopy // Journal of Lower Genital Tract Disease. 2023. Vol. 27, No. 1. P. 97–101.

[22] Willows K., et al. 2023 Canadian Colposcopy Guideline: a risk-based approach to management and surveillance of cervical dysplasia // Current Oncology. 2023. Vol. 30, No. 6. P. 431.

[23] Chen Y., et al. The value of endocervical curettage for diagnosis of cervical precancers or worse at colposcopy of women with atypical glandular cells cytology // Frontiers in Medicine. 2024. Vol. 11. Art. 1476361.

[24] Athanasiou A., Veroniki A. A., Efthimiou O., et al. Comparative effectiveness and risk of preterm birth of local treatments for cervical intraepithelial neoplasia and stage IA1 cervical cancer: a systematic review and network meta-analysis // Lancet Oncology. 2022. Vol. 23, No. 8. P. 1097–1108.

[25] Zhang L., Sauvaget C., Mosquera I., Basu P. Efficacy, acceptability and safety of ablative versus excisional procedure in the treatment of histologically confirmed CIN2/3: a systematic review // BJOG. 2023. Vol. 130, No. 2. P. 153–161.

[26] Adolph L., et al. Follow-up of women with cervical adenocarcinoma in situ treated by conization: a single centre clinical experience // Gynecologic Oncology. 2024.

[27] Carpini G. D., et al. Clinical outcomes of cervical adenocarcinoma in situ according to conservative or demolitive treatment: a systematic review and meta-analysis. 2025.

[28] Perkins R. B., Guido R. S., Castle P. E., et al. 2019 ASCCP Risk-Based Management Consensus Guidelines for abnormal cervical cancer screening tests and cancer precursors // Journal of Lower Genital Tract Disease. 2020. Vol. 24, No. 2. P. 102–131.

[29] Perkins R. B., et al. 2019 ASCCP Risk-Based Management Consensus Guidelines: updates through 2023 // Journal of Lower Genital Tract Disease. 2024.

[30] Håstad E., Aarnio R., et al. HPV testing alone as a test of cure after treatment with cervical loop excision: a retrospective register-based cohort study // Acta Obstetricia et Gynecologica Scandinavica. 2025.

[31] Sand F. L., Kjaer S. K., Frederiksen K., Dehlendorff C. Risk of recurrent disease following conization of cervical intraepithelial neoplasia grade 3 according to post-conization HPV status and surgical margins // Gynecologic Oncology. 2022. Vol. 166, No. 2. P. 341–347.

[32] Heydari F., et al. Long-term reassurance with negative high-risk human papillomavirus (HR-HPV) and clear margins after large loop excision of the transformation zone (LLETZ) // Cancers. 2025. Vol. 17, No. 3. Art. 487.

[33] Loopik D. L., IntHout J., Ebisch R. M. F., et al. The risk of cervical cancer after cervical intraepithelial neoplasia grade 3: a population-based cohort study with 80,442 women // Gynecologic Oncology. 2020. Vol. 157, No. 2. P. 319–325.

[34] Sawaya G. F., Lareau B., Lamar R. Monitoring after treatment of precancerous cervical lesions // JAMA Internal Medicine. 2026.

[35] Liu L., et al. Performance of artificial intelligence for diagnosing cervical intraepithelial neoplasia and cervical cancer: a systematic review and meta-analysis // EClinicalMedicine. 2025. Vol. 80. Art. 102992.

[36] Wang J., et al. Artificial intelligence enables precision diagnosis of cervical cytology grades and cervical cancer // Nature Communications. 2024. Vol. 15. Art. 4870.

[37] Wu T., et al. Artificial intelligence strengthens cervical cancer screening: present and future // Archives of Gynecology and Obstetrics. 2024.

[38] World Health Organization. WHO preferred product characteristics for therapeutic HPV vaccines. Geneva: WHO, 2024.

[39] Alouini S., et al. Therapeutic vaccines for HPV-associated cervical malignancies: a systematic review // JAMA Network Open. 2024.

[40] Khalil A. I., et al. Efficacy and safety of therapeutic HPV vaccines to treat CIN2/CIN3 lesions: a systematic review and meta-analysis of phase II/III clinical trials // BMJ Open. 2023. Vol. 13. Art. e068337.

[41] Eerkens A. L., et al. Vvax001, a therapeutic vaccine, for patients with HPV16-positive high-grade cervical intraepithelial neoplasia: a phase II trial // Clinical Cancer Research. 2025.

[42] Burdier F. R., Waheed D. N., Nedjai B., et al. DNA methylation as a triage tool for cervical cancer screening: a meeting report // Preventive Medicine Reports. 2024. Art. 102678.

[43] Schreiberhuber L., et al. Cervical cancer screening using DNA methylation triage in a real-world population // Nature Medicine. 2024.

[44] Gisca T., et al. Integrating biomarkers into cervical cancer screening: advances in diagnosis and risk prediction: a narrative review. 2025.

[45] Siewchaisakul P., et al. Genetic biomarkers associated with dynamic transitions of human papillomavirus (HPV) infection-precancerous-cancer of cervix for navigating precision prevention // International Journal of Molecular Sciences. 2025. Vol. 26. Art. 6016.

[46] Mortaki A., et al. The role of HPV genotyping, cytology, and methylation in the triage of high-risk HPV-positive patients // Biomedicines. 2025. Vol. 13. Art. 1139.

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Published

2026-04-21

How to Cite

Jumaniyazov , K. A., Bazarbaev , S. S., & Reymberganov , J. I. (2026). MODERN APPROACHES TO TREATMENT AND POST-TREATMENT MONITORING OF HPV-POSITIVE WOMEN WITH CERVICAL PATHOLOGY. International Journal of Cognitive Neuroscience and Psychology, 4(4), 17–26. https://doi.org/10.31149/ijnps.v4i4.2860

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