This trial examines the effect of HPV vaccination on reducing recurrence in patients post-surgery, indicating potential benefits for reproductive-age women.
Background: Persistent infection with high-risk human papillomavirus (HPV) after surgical management of high-grade squamous intraepithelial lesions (HSIL-CIN 2) is recognized as a major driver of recurrence and progression to cervical cancer.⁶ ¹⁰ Despite advances in screening and surgical techniques, recurrence rates remain clinically significant.⁵ ⁹ ¹⁰ Globally, cervical cancer continues to be one of the most common cancers affecting women, particularly in low- and middle-income countries.⁶ Although prophylactic HPV vaccines such as Gardasil® and Gardasil 9® were initially developed for primary prevention,³ ⁷ ⁸ emerging evidence suggests that they may also serve a secondary preventive role when administered after surgical treatment by reducing reinfection and supporting clearance of residual viral particles.¹ ² ⁴ ⁵ ⁹ Objective: This study aimed to assess whether postoperative administration of the quadrivalent HPV vaccine (Gardasil®) in reproductive-age women treated with CO₂ laser conization and vaporization for HSIL-CIN 2 could reduce recurrence of HPV infection and associated cytological abnormalities, thereby improving recurrence-free survival.
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Museridze et al. (2025) studied this question.
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