Oral Squamous Cell Carcinoma C01 C02 C03 C04 C05 C06
Conditions
Interventions
Group 1: Patient with histologically proven primary oral squamous cell carcinoma at one the participating hospitals diagnosed since 2005. Prospectively, the following parameters will be evaluated:
- T
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 18 years of age, histologically proven primary oral squamous cell carcinoma starting from 2005 or later, known TNM-status, sufficient diameter of tumor embedded in paraffin, informed consent
Exclusion criteria
Exclusion criteria: <18 years of age, no informed consent, not enough tumor (<5mm diameter) embedded in paraffin, no tam status
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Detection of prognostic biomarkers with tissue microarray for the outcome in patients with OSCC | — |
Secondary
| Measure | Time frame |
|---|---|
| Risk Factors alcohol, nicotine and drugs, nutrition, oral health status, TNM-classification, HPV-status, sex, age, date of recurrent cancer, type and duration of surgical and adjuvant oncological therapy, functional outcome, date of death, cause of death, oral hygiene. | — |
Countries
Germany
Contacts
Public ContactMax Heiland
Universitätsklinikum Hamburg-EppendorfMund-, Kiefer- und Gesichtschirurgie
Outcome results
None listed