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临床试验/NCT05179174
NCT05179174Unknown不适用

The Role of Genetic Mutations and of Circulating mRNAs in Uveal Melanoma

University of Catania3 个研究点 分布在 2 个国家目标入组 102 人开始时间: 2021年4月20日最近更新:
适应症

试验速览

阶段
不适用
入组人数
102
试验地点
3
主要终点
circulating GNA11 mutation detection through digital droplet PCR

研究概览

简要总结

The aim of the study is to identify genetic and epigenetic biomarkers in uveal melanoma, and to evaluate their diagnostic and prognostic role.

In particular, the specific objectives are:

  1. to identify the circulating somatic mutations associated with uveal melanoma;
  2. to identify the de-regulated miRNAs associated with uveal melanoma;
  3. to evaluate the diagnostic and prognostic role of the identified genetic and epigenetic markers;
  4. to identify possible therapeutic targets.

详细描述

This is a prospective, multicentric, case-control study, aimed at studying the gene and epigenetic mechanisms involved in uveal melanoma.

Patients with uveal melanoma, will be enrolled. For each subject included in the study, in a blood sample will be searched the mutations of the GNA11 and GNAQ genes and the expression of the following microRNAs: miR - 506-514 cluster, hsamiR - 592 and hsa - miR - 199a - 5p; the digital PCR droplet system will be used.

The study will not change the diagnostic-therapeutic process adopted in the clinical practice and will have no influence on the clinical management of enrolled patients.

A group of age sex matched controls will be recruited among patients scheduled for cataract surgery.

The sample size was calculated to detect, with a power of 80% and a confidence interval of 95%, a difference of 13.5% between the incidence of mutation of the GNA11 gene in patients with melanoma and healthy controls. (13.5% vs 0%). Overall, at least 51 patients with uveal melanoma and 51 controls will be recruited, for a total of at least 102 subjects.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • subjects diagnosed with uveal melanoma
  • both sexes
  • age ≥ 18 years

排除标准

  • a) autoimmune diseases
  • b) tumors
  • c) kidney diseases
  • d) atherosclerosis
  • e) subjects undergoing anti-inflammatory therapies.

结局指标

主要结局

circulating GNA11 mutation detection through digital droplet PCR

时间窗: at the diagnosis of uveal melanoma (first visit), through study completion, in an average of 1 year

the incidence of GNA11 mutations in uveal melanoma patients and in controls

次要结局

  • micro RNA levels in serum(at the diagnosis of uveal melanoma (first visit), through study completion, in an average of 1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Antonio Longo

Associate Professor

University of Catania

研究点 (3)

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