Detection of circulating tumor human papillomavirus DNA before diagnosis of HPV-positive head and neck cancer

被引:50
作者
Rettig, Eleni M. [1 ,2 ,3 ]
Faden, Daniel L. [3 ,4 ,5 ,6 ]
Sandhu, Shaiba [7 ]
Wong, Kristine [8 ]
Faquin, William C. [9 ]
Warinner, Chloe [3 ,4 ]
Stephens, Phil [10 ]
Kumar, Sunil [10 ]
Kuperwasser, Charlotte [10 ]
Richmon, Jeremy D. [3 ,4 ]
Uppaluri, Ravindra [1 ,2 ,3 ]
Varvares, Mark [3 ,4 ]
Sethi, Rosh [1 ,2 ,3 ]
Hanna, Glenn J. [2 ]
Sroussi, Herve [2 ,7 ]
机构
[1] Brigham & Womens Hosp, Div Otolaryngol Head & Neck Surg, 75 Francis St, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Ctr Head & Neck Oncol, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Otolaryngol Head & Neck Surg, Boston, MA 02115 USA
[4] Massachusetts Eye & Ear, Boston, MA USA
[5] Massachusetts Gen Hosp, Boston, MA 02114 USA
[6] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[7] Brigham & Womens Hosp, Div Oral Med & Dent, 75 Francis St, Boston, MA 02115 USA
[8] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[9] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[10] Naveris Inc, Natick, MA USA
关键词
circulating tumor DNA; head and neck cancer; human papillomavirus; oropharynx cancer; tumor-tissue-modified viral (TTMV) DNA;
D O I
10.1002/ijc.33996
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human papillomavirus (HPV), most commonly HPV16, causes a growing subset of head and neck squamous cell carcinomas (HNSCCs), including the overwhelming majority of oropharynx squamous cell carcinomas in many developed countries. Circulating biomarkers for HPV-positive HNSCC may allow for earlier diagnosis, with potential to decrease morbidity and mortality. This case-control study evaluated whether circulating tumor HPV DNA (ctHPVDNA) is detectable in prediagnostic plasma from individuals later diagnosed with HPV-positive HNSCC. Cases were participants in a hospital-based research biobank with archived plasma collected >= 6 months before HNSCC diagnosis, and available archival tumor tissue for HPV testing. Controls were biobank participants without cancer or HPV-related diagnoses, matched 10:1 to cases by sex, race, age and year of plasma collection. HPV DNA was detected in plasma and tumor tissue using a previously validated digital droplet PCR-based assay that quantifies tumor-tissue-modified viral (TTMV) HPV DNA. Twelve HNSCC patients with median age of 68.5 years (range, 51-87 years) were included. Ten (83.3%) had HPV16 DNA-positive tumors. ctHPV16DNA was detected in prediagnostic plasma from 3 of 10 (30%) patients with HPV16-positive tumors, including 3 of 7 (43%) patients with HPV16-positive oropharynx tumors. The timing of the plasma collection was 19, 34 and 43 months before cancer diagnosis. None of the 100 matched controls had detectable ctHPV16DNA. This is the first report that ctHPV16 DNA is detectable at least several years before diagnosis of HPV16-positive HNSCC for a subset of patients. Further investigation of ctHPV16DNA as a biomarker for early diagnosis of HPV16-positive HNSCC is warranted.
引用
收藏
页码:1081 / 1085
页数:5
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