Hoofd-hals plaveiselcelcarcinomen Head and neck cancer HPV+ head and neck squamous cell carcinoma (HNSCC)
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Patients should be at least 18 years of age - Patients should be able and willing to provide informed consent - Patients should have the clinical diagnosis of HNSCC - Tumour should be HPV positive - WHO performance status 0-2 - Patients are scheduled for: 1.Primary external beam radiotherapy (EBRT) 2.Primary EBRT with concurrent chemotherapy (Cisplatin);
Exclusion criteria
Exclusion criteria: - Any medical condition that may interfere with the study objectives - Positive test result for HIV or Hepatitis B or C - Any other active malignancy than cervical cancer.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To monitor the systemic effects of radiotherapy (RT) alone or in combination with concurrent chemotherapy (CRT) (Cisplatin) on the immune response and T-cells over time in patients with head and neck squamous cell carcinoma (HNSCC). T-cell fenotypic changes and T-cell related functional changes will be investigated. | — |
Secondary
| Measure | Time frame |
|---|---|
| - To compare the systemic immunological effect of RT alone to CRT in HNSCC patients. - To determine the optimal timing for future vaccination in HNSCC patients | — |
Countries
Netherlands