Human papillomavirus (HPV) load is higher in HPVDNA/p16 positive than in HPVDNA positive/p16 negative oropharyngeal squamous cell carcinoma but does not differ significantly between various subsites or correlate to survival

被引:1
作者
Zupancic, Mark [1 ,2 ]
Kostopoulou, Ourania N. [1 ]
Holzhauser, Stefan [1 ]
Lukoseviciute, Monika [1 ]
Jylha, Cecilia [3 ,4 ]
Marklund, Linda [2 ,5 ,6 ]
Nasman, Anders [1 ,7 ]
Sivars, Lars [3 ,8 ]
Dalianis, Tina [1 ,2 ,9 ]
机构
[1] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[2] Karolinska Univ Hosp, Med Unit Head Neck Lung & Skin Canc, Theme Canc, S-17176 Stockholm, Sweden
[3] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[4] Karolinska Univ Hosp, Dept Clin Genet, S-17176 Stockholm, Sweden
[5] Karolinska Inst, Dept Clin Sci Intervent & Technol CLINTEC, Div ENT Dis, Stockholm, Sweden
[6] Uppsala Univ, Dept Surg Sci, Sect Otolaryngol & Head & Neck Surg, Uppsala, Sweden
[7] Karolinska Univ Hosp, Dept Clin Pathol, Stockholm, Sweden
[8] Uppsala Univ, Dept Immunol Genet & Pathol, Uppsala, Sweden
[9] Karolinska Inst, Karolinska Univ Hosp, Dept Oncol Pathol & Mol Med & Surg, Bioclin J6 20, S-17164 Stockholm, Sweden
关键词
Human papillomavirus; Viral load; Oropharyngeal squamous cell carcinoma; P16; subsites; HIGH VIRAL LOAD; CANCER INCIDENCE; TONSILLAR CANCER; PHYSICAL STATUS; TONGUE CANCER; HEAD; BASE; PREVALENCE; EPIDEMIC; REVEALS;
D O I
10.1016/j.oraloncology.2024.106749
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Patients with human papillomavirus DNA positive (HPVDNA+) and p16ink4a overexpressing (p16+) oropharyngeal squamous cell carcinoma (OPSCC), especially those with cancer in the tonsillar and base of tongue subsites as compared to other OPSCC subsites have a better outcome than those with only HPVDNA+ or only p16+ cancer. Likewise having a high viral load has been suggested to be a positive prognostic factor. We therefore hypothesized, that HPV viral load could vary depending on OPSCC subsite, as well as with regard to whether the cancer was HPVDNA+ and p16+, or only HPVDNA+, or only p16+ and that this affected outcome. Material and methods: To address these issues HPV viral load was determined by HPV digital droplet (dd) PCR in tumor biopsies with previously known HPVDNA/p16 status from 270 OPSCC patients diagnosed 2000-2016 in Stockholm, Sweden. More specifically, of these patients 235 had HPVDNA+/p16+, 10 had HPVDNA+/p16-, 13 had HPVDNA-/p16+ and 12 had HPVDNA-/p16- cancer. Results: We found that HPVDNA+/p16+ OPSCC had a significantly higher viral load than HPVDNA+/p16- OPSCC. Moreover, there was a tendency for a higher viral load in the tonsillar and base of tongue OPSCC subsites compared to the other subsites and for a low viral load to correlate to a better clinical outcome but none of these tendencies reached statistical significance. Conclusion: To conclude, the mean viral load in HPVDNA+/p16+ OPSCC was higher than in HPVDNA+/p16OPSCC, but there was no statistically significant difference in viral load depending on OPSCC subsite or on clinical outcome.
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页数:7
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