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临床试验/NCT05798338
NCT05798338招募中不适用

Characterization of Extracellular Vesicles in Breast Cancer Patients' Plasma by Single Molecule Detection Array (SiMoA) Digital ELISA

Istituti Clinici Scientifici Maugeri SpA1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2020年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
105
试验地点
1
主要终点
EVs levels in early BC

研究概览

简要总结

Extracellular vesicles (EVs) are lipid bilayer-delimited particles, naturally released from cells and mediators of intercellular cross-talk. In breast cancer (BC), EVs seem to be involved in the tumor microenvironment's shaping, in cancer cells invasion and in the set-up of metastasis.

Clinical studies have provided initial evidence that these vesicles may have a prognostic and predictive value in breast cancer. Considering their ubiquitous presence in body fluids and their minimally invasive assessment through blood sampling, EVs could have a potential as liquid biopsy-derived biomarkers. Their quantification though is a complex task requiring complicated and time-consuming pre-analytical procedures of EVs isolation.

This protocol want to develop a new method for the detection of tumor-derived-EVs associated proteins, based on the use of Single Molecule Array (SiMoA), a digital ELISA technology able to detect and quantify extremely low concentrations of target proteins or particles.

The aim of this study is to evaluate how this new technology can allow the quantification of EVs plasma levels in patients affected by BC, providing useful diagnostic and prognostic information.

详细描述

This is a prospective, observational, monocentric and no profit study. The study involves the analysis of plasma from patients with breast cancer in order to quantify and characterize tumor-derived EVs at specific disease stages.

The enrollment of consecutive patients affected by BC referring to an EUSOMA-accredited Breast Unit is planned.

The patients will be divided into three pre-planned groups, as follows:

Population 1: patients diagnosed with early breast cancer patients (stage I-III) with indication to curative surgery.

Population 2: a control group made of sex- and age-matched healthy volunteers, not affected by cancer or chronic diseases.

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 90 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Signing of a specific informed consent for participation to the study
  • Female sex
  • Population 1:
  • Diagnosis of early breast cancer;
  • Indication for surgery after multidisciplinary discussion.
  • Population 2:
  • - Patients having a negative mammography or breast ultrasound within 12 months from the study enrollment.
  • Population 3:
  • Diagnosis of metastatic breast cancer confirmed by cytological/histological examination or by imaging;
  • Indication to chemotherapy.

排除标准

  • Population 1:
  • Presence of distant metastases
  • Synchronous presence of a different tumor
  • Indication to neoadjuvant chemotherapy
  • Population 2:
  • Diagnosis of breast cancer
  • Synchronous presence of a different tumor or chronic disease
  • Population 3:
  • - Patients who are unfit for systemic chemotherapy treatment

结局指标

主要结局

EVs levels in early BC

时间窗: 36 months

Determination of plasma EVs levels in patients with EBC by SIMOA digital ELISA and evaluation of the difference of their concentration compared to healthy controls

EVs levels in metastatic BC

时间窗: 36 months

Determination of plasma EVs levels in patients with first diagnosis of metastatic BC by SIMOA digital ELISA and evaluation of the difference of their concentration compared to healthy controls

次要结局

  • EVs levels after surgery(36 months)
  • EVs levels after chemotherapy treatment(36 months)

研究者

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

Fabio Corsi

Prof

Istituti Clinici Scientifici Maugeri SpA

研究点 (1)

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