Oropharyngeal Cancer, Human Papilloma Virus, and Clinical Trials

2010 ◽  
Vol 28 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Danny Rischin
2016 ◽  
Vol 130 (S2) ◽  
pp. S90-S96 ◽  
Author(s):  
H Mehanna ◽  
M Evans ◽  
M Beasley ◽  
S Chatterjee ◽  
M Dilkes ◽  
...  

AbstractThis is the official guideline endorsed by the specialty associations involved in the care of head and neck cancer patients in the UK. There has been significant debate in the management of oropharyngeal cancer in the last decade, especially in light of the increased incidence, clarity on the role of the human papilloma virus in this disease and the treatment responsiveness of the human papilloma virus positive cancers. This paper discusses the evidence base pertaining to the management of oropharyngeal cancer and provides recommendations on management for this group of patients receiving cancer care.Recommendations• Cross-sectional imaging is required in all cases to complete assessment and staging. (R)• Magnetic resonance imaging is recommended for primary site and computed tomography scan for neck and chest. (R)• Positron emission tomography combined with computed tomography scanning is recommended for the assessment of response after chemoradiotherapy, and has a role in assessing recurrence. (R)• Examination under anaesthetic is strongly recommended, but not mandatory. (R)• Histological diagnosis is mandatory in most cases, especially for patients receiving treatment with curative intent. (R)• Oropharyngeal carcinoma histopathology reports should be prepared according to The Royal College of Pathologists Guidelines. (G)• Human papilloma virus (HPV) testing should be carried out for all oropharyngeal squamous cell carcinomas as recommended in The Royal College of Pathologists Guidelines. (R)• Human papilloma virus testing for oropharyngeal cancer should be performed within a diagnostic service where the laboratory procedures and reporting standards are quality assured. (G)• Treatment options for T1–T2 N0 oropharyngeal squamous cell carcinoma include radical radiotherapy or transoral surgery and neck dissection (with post-operative (chemo)radiotherapy if there are adverse pathological features on histological examination). (R)• Transoral surgery is preferable to open techniques and is associated with good functional outcomes in retrospective series. (R)• If treated surgically, neck dissection should include levels II–IV and possibly level I. Level IIb can be omitted if there is no disease in level IIa. (R)• If treated with radiotherapy, levels II–IV should be included, and possibly level Ib in selected cases. (R)• Altering the modalities of treatment according to HPV status is currently controversial and should be undertaken only in clinical trials. (R)• Where possible, patients should be offered the opportunity to enrol in clinical trials in the field. (G)


2020 ◽  
Vol 106 (5) ◽  
pp. 893-899 ◽  
Author(s):  
Danielle N. Margalit ◽  
Sana D. Karam ◽  
Melvin L.K. Chua ◽  
Carryn Anderson ◽  
Randall J. Kimple

2015 ◽  
Vol 86 (6) ◽  
pp. 442-447 ◽  
Author(s):  
Lisa Buckley ◽  
Ruta Gupta ◽  
Bruce Ashford ◽  
Joe Jabbour ◽  
Jonathan R. Clark

2016 ◽  
Vol 130 (11) ◽  
pp. 1048-1053 ◽  
Author(s):  
O T Dale ◽  
S Sood ◽  
K A Shah ◽  
C Han ◽  
D Rapozo ◽  
...  

AbstractObjective:This study investigated long-term survival outcomes in surgically treated oropharyngeal cancer patients with known human papilloma virus status.Methods:A case note review was performed of all patients undergoing primary surgery for oropharyngeal cancer in a single centre over a 10-year period. Human papilloma virus status was determined via dual modality testing. Associations between clinicopathological variables and survival were identified using a log-rank test.Results:Of the 107 cases in the study, 40 per cent (n = 41) were human papilloma virus positive. The positive and negative predictive values of p16 immunohistochemistry for human papilloma virus status were 57 per cent and 100 per cent, respectively. At a mean follow up of 59.5 months, 5-year overall and disease-specific survival estimates were 78 per cent and 69 per cent, respectively. Human papilloma virus status (p = 0.014), smoking status (p = 0.021) and tumour stage (p = 0.03) were significant prognostic indicators.Conclusion:The long-term survival rates in surgically treated oropharyngeal cancer patients were comparable to other studies. Variables including human papilloma virus status and tumour stage were associated with survival in patients treated with primary surgery; however, nodal stage and presence of extracapsular spread were non-prognostic.


2013 ◽  
Vol 106 ◽  
pp. S51-S52
Author(s):  
W. Pongsapich ◽  
S. Siritantikorn ◽  
P. Jotikaprasardhna ◽  
A. Pumchan ◽  
C. Chongkolwatana

2022 ◽  
Vol 12 (1) ◽  
Author(s):  
Ken Akashi ◽  
Toshihiko Sakai ◽  
Osamu Fukuoka ◽  
Yuki Saito ◽  
Masafumi Yoshida ◽  
...  

AbstractIn head and neck cancer, early detection of recurrence after treatment is important. The contemporary development of therapeutic agents have improved the prognosis after recurrence; however, no biomarker has been established for evaluating therapeutic effects or detecting recurrence. Recently, circulating tumor DNA (ctDNA), which comprises DNA derived from tumor cells and exists in the form of cell-free DNA in the blood, has attracted attention as a minimally invasive and repeatable biomarker for detecting cancer. We validated the usefulness of ctDNA of human papilloma virus (HPV)-derived sequences as a biomarker in HPV-related p16-positive oropharyngeal cancer by assessing 25 patients with p16-positive oropharyngeal cancer. Blood samples were collected from each patient at multiple time points during the treatment, and the plasma was preserved. The ctDNA was extracted from the plasma and analyzed using digital polymerase chain reaction. HPV-derived ctDNA was detected in 14 (56%) of the 25 patients. In all the patients, the samples were found to be ctDNA-negative after initial treatment. Cancer recurrence was observed in 2 of the 14 patients; HPV-derived ctDNA was detected at the time of recurrence. Our results indicate that HPV-derived ctDNA can be a prospective biomarker for predicting the recurrence of p16-positive oropharyngeal cancer.


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