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临床试验/NCT06047236
NCT06047236
招募中
不适用

Immune Biomarker Study for Salivary Gland Carcinoma

University of Erlangen-Nürnberg Medical School2 个研究点 分布在 1 个国家目标入组 300 人2024年1月8日

概览

阶段
不适用
干预措施
Sampling
疾病 / 适应症
Salivary Gland Tumor
发起方
University of Erlangen-Nürnberg Medical School
入组人数
300
试验地点
2
主要终点
Progression-free survival (PFS)
状态
招募中
最后更新
上个月

概览

简要总结

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.

注册库
clinicaltrials.gov
开始日期
2024年1月8日
结束日期
2031年9月30日
最后更新
上个月
研究类型
Observational
性别
All

研究者

发起方
University of Erlangen-Nürnberg Medical School
责任方
Sponsor

入排标准

入选标准

  • Observational group
  • Initial diagnosis of a primary salivary gland carcinoma in the head and neck region (no squamous cell carcinomas)
  • Specimen collection from the center of the tumor when the primary tumor is sufficiently large without that the pathological assessment is impaired
  • Control group 1
  • Initial diagnosis of a benign salivary gland tumor in the head and neck region
  • Specimen collection from the center of the tumor when the primary tumor is sufficiently large without that the pathological assessment is impaired
  • Control group 2
  • functional diseases of the nose or ear (patients with the indication for functional ear surgery and rhinoplasty)
  • Specimen collection with sufficiently large resectate during a functional nose surgery
  • for all groups:

排除标准

  • Distant metastasis at the time of diagnosis and simultaneous second cancers, i.e. at study inclusion
  • Malignancy in the last 5 years regardless of location (except basal cell carcinoma or cis of the uterine cervix)
  • Carcinomas for which specimen collection is not possible or likely without compromising the compromise the pathological evaluation
  • Persistent drug or medication abuse
  • Patients who are unable or unwilling to comply with protocol and to be treated
  • Patients who are represented by a legal guardian
  • Patients who are not suitable for participation in the study due to a language barrier

研究组 & 干预措施

Malignant salivary gland tumor in the head and neck region

Initial diagnosis of primary salivary gland carcinoma in the head and neck region

干预措施: Sampling

Benign salivary gland tumor in the head and neck region

Initial diagnosis of a benign salivary gland tumor in the head and neck region

干预措施: Sampling

functional disorders of the nose or ear

Healthy control group. Functional diseases of the nose or ear (patients with the indication for functional ear surgery and rhinoplasty) without salivary gland tumor.

干预措施: Sampling

结局指标

主要结局

Progression-free survival (PFS)

时间窗: 2 years

As a primary clinical endpoint, the progression-free survival (PFS) of the patients in the observational cohort will be analyzed after two years.

次要结局

  • Locoregional recurrence rate (LRR)(From baseline to the end of study period, up to 5 years)
  • Occurrence of distant metastases(From baseline to the end of study period, up to 5 years)
  • Longitudinal immunophenotyping of the patients: Detection of about 30 distinct immune cell (sub)types together with their activation markers during study period(Change of the immunophenotyping from baseline to the end of study period, up to 5 years)
  • Immune status of the resected tumor(1 year)
  • Transcriptional changes in immune cell gene expression(Change of the immunophenotyping from baseline to the end of study period, up to 5 years)
  • Analysis of patient's microbiomic state by examination of saliva, tumor and stool(The analyses are conducted from baseline to the end of study period, up to 5 years)
  • Analysis of cytokines and metabolites in peripheral blood and their change at certain points in the course of treatment(Change of the cytokine expression from baseline to the end of study period, up to 5 years)

研究点 (2)

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