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Updated: Apr 24, 2026

Chromogenic In Situ Hybridization as a Tool for HPV-Related Head and Neck Cancer Diagnosis
Published on: June 14, 2019
HPV Genotypes and Survival Outcomes in Invasive Cervical Cancer: A Retrospective Molecular Analysis of FFPE Clinical
Mohammad Hossein Darvishali1, Haniyeh Nikkhah1, Hossein Rahavi2
1Stem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Background:
High-risk human papillomavirus (HPV) genotypes differ in carcinogenic potential and may be associated with distinct clinical and survival outcomes in invasive cervical cancer.
Methods:
Tumor DNA was extracted from formalin-fixed paraffin-embedded (FFPE) cervical cancer samples (N = 120). HPV genotyping was then performed using a type-specific molecular assay (SENMURV HPV Genotyping Kit, Stem Cell Technology Co., Iran). The identified genotypes were subsequently grouped for survival analysis (HPV16 alone, HPV16 co-infection, HPV18-containing, and mixed infections with ≥3 types). Clinicopathologic and follow-up data were obtained from medical records, and overall survival was analyzed using Kaplan-Meier estimates and Cox proportional hazards models.
Results:
Single HPV16 infection was the predominant genotype pattern across the histologic subtypes, whereas HPV18-containing and multiple-genotype infections were less frequent and showed a non-significant trend toward poorer early survival. In multivariable Cox regression analysis, age remained the only independent predictor of overall survival (HR = 1.035; 95% CI: 1.005-1.065; p = 0.020), while histologic subtype and HPV genotype were not statistically significant. Overall, 33 deaths were observed during follow-up in the study cohort.
Conclusion:
Although no statistically significant associations were observed, HPV genotype-specific patterns suggested potential differences in survival, particularly for HPV18-containing infections. As exploratory, hypothesis-generating findings, these results highlight the need for larger, multicenter cohorts to clarify the independent prognostic role of HPV genotypes alongside established clinical factors.
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