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Efficacy Analysis of Paiteling in Treating Persistent High-Risk Human Papillomavirus after Cervical Cancer Surgery.

Created on 07 Jul 2026

Authors

Zhuo'er Li, Meijun Li, Mengdie Tian, Min Zhou, Chunli Wang, Zhiqiang Guo

Published in

Journal of visualized experiments : JoVE. Issue 232. Jun 16, 2026. Epub Jun 16, 2026.

Abstract

Persistent infection with high-risk human papillomavirus (HR-HPV) following cervical cancer surgery poses a significant risk for disease recurrence and progression to vaginal intraepithelial neoplasia. This retrospective cohort study evaluated the comparative efficacy of Paiteling, a Traditional Chinese Medicine compound, versus recombinant human interferon gel in treating persistent HR-HPV infection post-hysterectomy. Thirty-six patients with persistent HR-HPV positivity were allocated to either Paiteling (n = 17) or interferon (n = 19) treatment groups. Comprehensive assessment included HPV DNA load, ThinPrep cytologic test results, and colposcopic findings at baseline, 6-month, and 12-month follow-ups. At 6 months, the interferon group demonstrated significantly higher cure rates (68.4% vs 17.6%, 2= 7.646, p = 0.006). However, a remarkable reversal was observed at 12 months, with Paiteling achieving superior clearance rates (94.1% vs 63.2%, 2=4.976, p = 0.044). Multivariable analysis confirmed Paiteling treatment as a strong predictor of HPV clearance (adjusted OR = 9.52, 95% CI: 1.11-220.32, p = 0.039). Subgroup analysis revealed consistent treatment effects across all HPV genotypes. Adverse events were mild and self-limiting, with no significant differences between groups (29.4% vs 10.5%, p. = 0.226). This study demonstrates Paiteling's superior long-term efficacy for persistent postoperative HR-HPV infection, characterized by a unique delayed-but-sustained response pattern. The multi-targeted mechanism, favorable safety profile, and sustained viral clearance support Paiteling's potential as an effective therapeutic option in postoperative management, though validation through larger prospective trials is warranted.

PMID:
42406849
Bibliographic data and abstract were imported from PubMed on 07 Jul 2026.

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