About this trial
This observational study will evaluate whether salivary interleukin-6 levels and selected interleukin gene polymorphisms are associated with regional lymph node involvement in patients with oral squamous cell carcinoma.
Adult patients with histologically confirmed oral squamous cell carcinoma will be enrolled before receiving any cancer-specific treatment. Participants will be classified into two groups according to the presence or absence of regional lymph node metastasis: OSCC N0M0 and OSCC N+M0.
The study does not involve any experimental treatment and does not change the standard diagnostic or therapeutic pathway. Each participant will provide a saliva sample using a sterile absorbent swab. The saliva sample will be used to measure interleukin-6 levels. Available biological material will also be used to analyze selected interleukin gene polymorphisms, including IL6, IL1B, IL10, IL8/CXCL8, and IL1RN.
The aim of the study is to explore whether these salivary and genetic markers may help characterize different biological patterns of locoregional progression in oral squamous cell carcinoma.
Eligibility criteria
Qualifiers
Age 18 years or older
Histopathologically confirmed diagnosis of oral squamous cell carcinoma of the oral cavity
Oral squamous cell carcinoma site excluding oropharyngeal sites
Defined regional lymph node status allowing classification as OSCC N0M0 or OSCC N+M0
Disqualifiers
Age younger than 18 years
Oral squamous cell carcinoma involving oropharyngeal sites
Presence of distant metastasis
Previous OSCC-specific oncological treatment before saliva sample collection
Trial design
Treatments tested in this trial
- Saliva Collection and Biomarker Analysis