Human Papillomavirus DNA Detection by Droplet Digital PCR in Formalin-Fixed Paraffin-Embedded Tumor Tissue from Oropharyngeal Squamous Cell Carcinoma Patients

被引:8
作者
Schiavetto, Camila Marques [1 ]
de Abreu, Priscila Marinho [2 ]
von Zeidler, Sandra Ventorin [2 ]
de Jesus, Lais Machado [1 ]
Carvalho, Raiany Santos [3 ]
Cirino, Maria Thereza [1 ]
Carloni, Adriana Cruvinel [1 ]
Oliveira, Cristina [1 ]
Scapulatempo-Neto, Cristovam [1 ,4 ]
de Almeida, Gisele Caravina [4 ,5 ]
de Menezes, Nei Soares [5 ]
Carvalho, Andre Lopes [1 ]
Reis, Rui Manuel [1 ,6 ,7 ]
de Carvalho, Ana Carolina [1 ]
机构
[1] Barretos Canc Hosp, Mol Oncol Res Ctr, Rua Antenor Duarte Vilela 1331, BR-14784400 Barretos, SP, Brazil
[2] Univ Fed Espirito Santo, Programa Posgrad Biotecnol, Ctr Ciencias Saude, Vitoria, ES, Brazil
[3] Barretos Canc Hosp, Res Support Ctr, Sao Paulo, Brazil
[4] Diagnost Amer DASA, Pathol & Mol Diagnost Serv, Sao Paulo, Brazil
[5] Barretos Canc Hosp, Dept Pathol, Sao Paulo, Brazil
[6] Univ Minho, Sch Med, Life & Hlth Sci Res Inst ICVS, Braga, Portugal
[7] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
基金
巴西圣保罗研究基金会;
关键词
IN-SITU HYBRIDIZATION; E6/E7; MESSENGER-RNA; NECK-CANCER; HPV DNA; P16; IMMUNOHISTOCHEMISTRY; STAGING SYSTEM; ORAL-CAVITY; HEAD; SURVIVAL; ASSOCIATION;
D O I
10.1007/s40291-020-00502-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Introduction High-risk human papillomavirus infection impacts staging and prognosis of oropharyngeal squamous cell carcinomas (OPSCCs). Determination of HPV status in tumor tissue by p16-immunohistochemistry (p16-IHC) can be challenging; therefore, complementary methodologies could be useful in a clinical setting. Objective To test for accuracy and clinical relevance of HPV-DNA detection in formalin-fixed and paraffin-embedded (FFPE) tumor samples by droplet digital PCR (ddPCR). Materials and Methods Fifty OPSCCs were tested for p16-IHC status followed by HPV-16/18 DNA detection/quantification in FFPE-recovered DNA using ddPCR. Accuracy for HPV status determination and association with patient information were also evaluated. Results 32.0% (16/50) of the cases were p16-IHC positive (p16 +), 42.0% (21/50) had detectable levels of HPV-16 DNA, and none were positive for HPV-18 DNA. A higher median viral load of HPV-16 DNA was observed in p16 + cases (p < 0.0001). Concordance between p16-IHC and HPV-16 DNA ranged from 78.0 to 86.0% and accuracy rates were between 78.0 and 86.0%. P16-IHC and HPV-16 DNA detection was associated with gender, smoking status, and tumor subsite, while only HPV-16 DNA was associated with cT stage. The combination of HPV positivity by p16-IHC and ddPCR showed higher overall survival rates in comparison with p16 + /HPV-DNA- and p16 - /HPV-DNA- results. Conclusions Type-specific HPV-DNA detection by ddPCR is highly specific but moderately sensitive for the determination of HPV status and showed clinical relevance, mainly when associated with p16-IHC status. Results highlight the importance of performing HPV-DNA testing in combination with p16-IHC for proper identification of HPV-associated OPSCC and to improve clinical management of OPSCC patients.
引用
收藏
页码:59 / 70
页数:12
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