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The immunological aspects of conventional therapy ((chemo)radiation) for the treatment of head and neck squamous cell carcinoma (HNSCC): an exploratory study.

The immunological aspects of conventional therapy ((chemo)radiation) for the treatment of head and neck squamous cell carcinoma (HNSCC): an exploratory study. - IMRAD

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON40292
Enrollment
20
Registered
2015-01-14
Start date
2015-04-14
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hoofd-hals plaveiselcelcarcinomen Head and neck cancer HPV+ head and neck squamous cell carcinoma (HNSCC)

Interventions

None listed

Sponsors

Antoni van Leeuwenhoek Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

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

MeasureTime 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

MeasureTime 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

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)