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

Overview

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.

Detailed description

Statistical analyse Plan: All data will be log-transformed to approximate normal distribution. For pairwise comparisons Student's t-test will be used. For multiple comparisons one-way ANOVA followed by a suitable post-hoc test will be performed.

Power: Power has been determined based on available previous data. The investigator will have access to samples from up to 300 study subjects that can be used generate different datasets. The calculated sample size ranges from 20 to 60 samples per group depending on the specific research question. This calculation was conducted assuming two-tailed comparisons, with, significance p\<0.05, and power 80%.

Interventions

• Procedure Sentinel Node detection and Biopsy
  Fine Needle aspiration from sentinel Lymph Nodes

Primary outcome measures

• Proportion of cervical lymph nodes with tumor cells detected by flow cytometry [Time frame: Baseline (at surgery or biopsy)]
• Immunological cell profile in sentinel node measured by flow cytometry [Time frame: Baseline (at surgery or biopsy)]

Secondary outcome measures (1)

• Differential gene expression between sentinel node and non tumour draining lymph node. [Time frame: Baseline (at surgery or biopsy)]

Eligibility criteria

Inclusion criteria

• a diagnosis of primary HNSCC,
• tumor excision combined with a sentinel node-assisted elective neck dissection or sentinel node biopsy alone performed at Karolinska University Hospital, Stockholm, Sweden
• willingness to participate in the study.

Exclusion criteria

• systematic autoimmune diseases
• synchronous or previous second malignancies or hemo-lymphopoietic malignancies
• any other acute or chronic condition that could influence the immunological environment in the lymph nodes.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model

Other

Study locations

Sweden · 1 center

• Karolinska University Hospital — Stockholm

Identifiers

NCT: NCT07131566 · Vetenskapsrådet 2024-03236 · K 2022-2823

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗