Actively Recruiting

Age: 18Years +
All Genders
NCT07131566

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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Immune Response in Cervical Lymph Nodes of Patients With Head and Neck Cancer | DecenTrialz