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Human Papilloma Virus in Head and Neck Cancer: Clinico-pathological Outcome

Not Applicable
Conditions
Health Condition 1: null- Head and Neck Cancers - HPV presence and viral load estimstion
Registration Number
CTRI/2013/04/003525
Lead Sponsor
Cancer Centre Welfare Home and Research Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
150
Inclusion Criteria

All patients diagnosed as suffering from HNSCC presenting in the Institute

Exclusion Criteria

1) Immunocompromised patients:

a) Previous chemotherapy due to any cancer

b) Immunodeficiency status-latrogenic or disease indused

2) Previous Radiotherapy due to any cause

3) Where adequate biopsy sample cannot be obtained due to technical reasons

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
HPV type and load related differences in disease progression and treatment response in HNSCCTimepoint: 3 years of recruitment followed by further 2 yrs of of follow up after the last recruitment.
Secondary Outcome Measures
NameTimeMethod
Site of Recurrence and time interval of recurrence following treatment of HNSCC dependant on HPV Subtype and viral load.Timepoint: 3 years of recruitment followed by further 2-5 yrs of of follow up after the last recruitment.
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