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Significance of HPV16 Viral Load Testing in Anal Cancer

Authors :
Tomasz Rutkowski
Ewa Chmielik
Ewa Małusecka
Monika Giglok
Rafał Suwiński
Dariusz Lange
Agnieszka M. Mazurek
Source :
Pathology Oncology Research
Publication Year :
2020
Publisher :
Springer Science and Business Media LLC, 2020.

Abstract

Human papilloma virus (HPV) is highly frequent among patients with anal squamous cell carcinoma, but the viral load (VL) differs between patients. This study aimed to compare the rate of HPV positivity, HPV16VL, p16INK4A and p53 expression between treatment naive and recurrent anal cancer patients. HPV was genotyped via AmpliSens® HPV HCR-genotype-titre-FRT kit. HPV16 VL was determined via quantitative polymerase chain reaction-based in-house test. p16INK4A and p53 expression was tested via immunohistochemistry. The cohort comprised 13 treatment-naive and 17 recurrent anal SCC patients. High-risk HPV was detected in 87% of cases, and HPV16 (73%) was the predominant genotype. The rate of HPV positivity was higher among women and nonsmokers, and majority of HPV-positive cases were also p16INK4A-positive. All p53-negative tumors were HPV16-positive. The most predominant p53 staining pattern in the HPV-positive group was scattered type, whereas it was diffuse type in the HPV-negative group. The HPV16 VL was higher in the treatment-naive group. Further, in the treatment-naive group, cases with scattered staining pattern of p53 had higher HPV16 VL than cases with diffuse staining pattern. The opposite result was noted in the recurrent cancer group. Moreover, p16-positive cases with scattered p53 staining pattern in the treatment naive group had higher HPV16 VL than their counterparts in the recurrent cancer group. In conclusion, the HPV VL, as is the association between VL and p16INK4A /p53, is in an inversed trend in treatment naive and recurrent cancer patients, highlighting the importance of HPV VL measurement in anal SCC.

Details

ISSN :
15322807 and 12194956
Volume :
26
Database :
OpenAIRE
Journal :
Pathology & Oncology Research
Accession number :
edsair.doi.dedup.....51bceaf73a29afaba888bc5a8107f826
Full Text :
https://doi.org/10.1007/s12253-020-00801-7