Human papillomavirus infection and immunohistochemical p16INK4a expression as predictors of outcome in penile squamous cell carcinomas

Summary Approximately 50% of penile squamous cell carcinomas (SCC) are associated with high-risk human papillomavirus (HR-HPV) infection. We evaluated the correlation of p16INK4a expression and HR-HPV with clinicopathological features and outcome in a cohort of patients with penile SCC. Two tissue m...

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Veröffentlicht in:Human pathology 2015-04, Vol.46 (4), p.532-540
Hauptverfasser: Bezerra, Stephania M., MD, Chaux, Alcides, MD, Ball, Mark W., MD, Faraj, Sheila F., MD, Munari, Enrico, MD, Gonzalez-Roibon, Nilda, MD, Sharma, Rajni, PhD, Bivalacqua, Trinity J., MD, Burnett, Arthur L., MD, Netto, George J., MD
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Sprache:eng
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Zusammenfassung:Summary Approximately 50% of penile squamous cell carcinomas (SCC) are associated with high-risk human papillomavirus (HR-HPV) infection. We evaluated the correlation of p16INK4a expression and HR-HPV with clinicopathological features and outcome in a cohort of patients with penile SCC. Two tissue microarrays were constructed from 53 invasive penile SCC at our hospital. p16INK4a expression was assessed by immunohistochemistry (CINtec Kit). High-risk human papillomavirus status was assessed by in situ hybridization (INFORM HPV III family 16 probe B cocktail). High-risk human papillomavirus was detected in 8 cases (15%), and p16INK4a overexpression was found in 23 cases (44%). Both markers showed a significant association with histologic subtype ( P = .017 and P = .01, respectively) and lymphovascular invasion ( P = .015 and P = .015, respectively). Regarding outcome analyses, neither HPV infection nor p16INK4a overexpression significantly predicted overall survival or cancer-specific survival using Cox proportional hazards regression model. High-risk human papillomavirus positivity and p16INK4a overexpression were significantly associated with histologic subtype and presence of lymphovascular invasion. Human papillomavirus status was not predictive of outcome in our cohort.
ISSN:0046-8177
1532-8392
DOI:10.1016/j.humpath.2014.12.004