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临床试验/NCT05720676
NCT05720676尚未招募不适用

Clinical, Histopathological, Molecular and Experimental Characterization of Liver Metastases From Patients With Breast Cancer.

KU Leuven1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年3月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
KU Leuven
入组人数
20
试验地点
1
主要终点
To determine the levels and patterns of immune infiltrates in liver metastases from BC patients

研究概览

简要总结

The goal of this observational study is to learn about breast cancer liver metastasis in patients who met the following criteria:

  • female;
  • be ≥ 18 years of age on the day of signing informed consent;
  • confirmed diagnosis of breast cancer liver metastases. Newly diagnosed patients with de-novo liver metastases are eligible;
  • be planned for liver surgery.

The main questions it aims to answer are:

  1. To characterize the tumour cells and their microenvironment in the liver metastases at the transcriptomic and protein single-cell level;
  2. To determine the levels and patterns of immune infiltrates in liver metastases from BC patients;
  3. To identify biological features associated with the histopathological growth patterns in liver metastases.
  4. To create patient-derived xenografts (PDX) and organoids (PDO) from liver metastases isolated from patients with BC;
  5. To perform a histopathological and molecular comparison of liver metastases, PDX and PDO isolated from the same patient

Participants will be willing and able to provide written informed consent for this study and tissue samples for research purposes.

研究设计

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

入排标准

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

入选标准

  • be willing and able to provide written informed consent for this study;
  • be ≥ 18 years of age on the day of signing informed consent;
  • confirmed diagnosis of breast cancer liver metastases. Newly diagnosed patients with de-novo liver metastases are eligible;
  • be planned for liver surgery;
  • be willing to provide tissue samples for research purposes.

排除标准

  • unwillingness to provide the samples or clinical information needed for the study;
  • History of radiofrequency destruction (RF), stereotactic Body Radiotherapy (SBRT) or intra-arterial treatment such as chemoembolization (TACE) or selective internal radiation therapy (SIRT) performed on the metastasis to be examined (accepted if performed in other metastasis);
  • Has an active autoimmune disease that has required systemic treatment in the past 2 years prior to the surgery (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment;
  • Presence of immunodeficiency or immune dysregulatory diseases and conditions which require active immune modulatory treatment of any kind, or required treatment in the past two years from date of diagnosis of breast cancer;
  • History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results in the opinion of the treating investigator.

结局指标

主要结局

To determine the levels and patterns of immune infiltrates in liver metastases from BC patients

时间窗: 2 years

To characterize the tumour cells and their microenvironment in the liver metastases at the transcriptomic and protein single-cell level.

时间窗: 2 years

To identify biological features associated with the histopathological growth patterns in liver metastases.

时间窗: 2 years

To create patient-derived xenografts (PDX) and organoids (PDO) from liver metastases isolated from patients with BC

时间窗: 2 years

To perform a histopathological and molecular comparison of liver metastases, PDX and PDO isolated from the same patient.

时间窗: 2 years

To investigate the histopathological growth patterns of liver metastases using intra-vital imaging of these metastases in PDX.

时间窗: 2 years

To use PDX and PDO to evaluate the efficacy of various treatments.

时间窗: 2 years

次要结局

未报告次要终点

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Sophia Leduc

PhD Student

KU Leuven

研究点 (1)

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