Actively Recruiting
Immune Response in Cervical Lymph Nodes of Patients With Head and Neck Cancer
Led by Lars Olaf Cardell · Updated on 2025-08-20
500
Participants Needed
1
Research Sites
560 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Objective: The aim of this study is to characterize the inflammatory response in patients with head and neck cancer. More specifically, the study intend to investigate inflammatory and genetic differences between the primary tumor, the sentinel lymph node, and other regional lymph nodes. The investigator also aim to assess how the immunological and genetic responses differ in lymph nodes with and without metastases. To enable the detection of metastases in lymph nodes containing very few cancer cells, the investigator are developing a method to identify tumor cells using flow cytometry. Additionally, both tumor tissue and lymph nodes will undergo in vitro testing of checkpoint blockade therapy, a relatively new form of cancer immunotherapy. Methods: Biopsies from the primary tumor will be used to assess local inflammation. Fine-needle aspirates and dissected lymph node tissue will be analyzed to study inflammatory and genetic responses, as well as to detect tumor cells within these nodes. Blood samples from patients with head and neck cancer will be analyzed for inflammatory mediators. Lymph nodes from patients without cancer will be collected during benign neck surgeries. Immunological and genetic parameters from these control lymph nodes will be compared to those from the cancer patients to identify disease-specific patterns.
CONDITIONS
Official Title
Immune Response in Cervical Lymph Nodes of Patients With Head and Neck Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of primary head and neck squamous cell carcinoma (HNSCC)
- Undergoing tumor excision combined with sentinel node-assisted elective neck dissection or sentinel node biopsy alone at Karolinska University Hospital, Stockholm, Sweden
- Willingness to participate in the study
You will not qualify if you...
- Presence of systemic autoimmune diseases
- Having synchronous or previous second malignancies or blood-related cancers
- Any other acute or chronic condition that could affect the immune environment in lymph nodes
AI-Screening
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Trial Site Locations
Total: 1 location
1
Karolinska University Hospital
Stockholm, Stockholm County, Sweden, 17176
Actively Recruiting
Research Team
L
Lars Olaf Cardell, Professor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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