Actively Recruiting

Age: 18Years +
All Genders
NCT06047236

Immune Biomarker Study for Salivary Gland Carcinoma

Led by University of Erlangen-Nürnberg Medical School · Updated on 2026-03-16

300

Participants Needed

2

Research Sites

403 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Salivary gland carcinomas (SGC) are rare tumors. The term SGC is not more than an umbrella for a variety of histogenetically, morphologically, and biologically distinct entities. Accordingly, SGCs have not been sufficiently investigated to date. Their rarity makes it challenging to recruit a high number of patients for individual entities in clinical studies, leading to the pooling of patients with different histological subtypes to achieve sufficient participants. The different histological subtypes of SGC exhibit significant differences in their clinicopathological features, including grading, occurrence, and outcome. SGCs usually are stratified into low-, intermediate-, or high-grade tumors. In most kinds of SGC, specific targetable molecular markers are lacking. The inclusion of immunotherapy (IT), however, might improve the outcome of patients suffering from high-grade SGCs. To integrate IT as a therapeutic option for SGC and to facilitate informed therapeutic decisions based on tumor (immune) biology, predictive and prognostic immunological biomarkers are indispensable. In this prospective study, 500 patients will be enrolled, distributed across three arms. The observational cohort includes patients with malignant salivary gland tumors, whereas patients with benign tumors of a salivary gland are grouped in the control group 1. In the control cohort, two patients do not have a salivary gland tumor but have a planned functional surgery of the nose or ear or a maxillofacial surgery. The local immune status of the tumor tissue and the microbiome will be sampled before treatment. In addition, the systemic immune status from peripheral blood will be analyzed before and after surgery and after the adjuvant and definitive chemoradiotherapy (CRT), if applicable. Clinical baseline characteristics and outcome parameters will additionally be collected. Data mining and modeling approaches will be applied to identify interactions between local and systemic immune parameters and to define predictive and prognostic immune signatures based on the evaluated immune markers.

CONDITIONS

Official Title

Immune Biomarker Study for Salivary Gland Carcinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Initial diagnosis of a primary salivary gland carcinoma in the head and neck region (no squamous cell carcinomas) for observational group
  • Specimen collection possible from the center of the tumor when large enough without impairing pathological assessment
  • Initial diagnosis of a benign salivary gland tumor in the head and neck region for control group 1
  • Functional diseases of the nose or ear with planned functional ear surgery or rhinoplasty for control group 2
  • Willingness to provide blood, saliva, and stool samples and consent to preservation of samples for study
  • Age 18 years or older
  • Sufficient cognitive ability to understand and agree to the study purpose
Not Eligible

You will not qualify if you...

  • Presence of distant metastasis or simultaneous second cancers at diagnosis
  • Any malignancy in the last 5 years except basal cell carcinoma or carcinoma in situ of the uterine cervix
  • Tumors where specimen collection would compromise pathological evaluation
  • Persistent drug or medication abuse
  • Inability or unwillingness to comply with the study protocol
  • Being represented by a legal guardian
  • Unsuitability for study participation due to language barriers

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Universitätsklinikum Erlangen, HNO

Erlangen, Bavaria, Germany, 91054

Actively Recruiting

2

Universitätsklinikum Erlangen, Strahlenklinik

Erlangen, Bavaria, Germany, 91054

Actively Recruiting

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Research Team

S

Studiensekretariat

CONTACT

T

Translation Radiobiology

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

3

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