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临床试验/NCT04892433
NCT04892433招募中不适用

Tissue Study in Patients Undergoing CAR-T Cell Therapy

IRCCS Azienda Ospedaliero-Universitaria di Bologna1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年5月14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
150
试验地点
1
主要终点
Study of epigenetics

研究概览

简要总结

The "CAR-T" immunotherapy ("Chimeric Antigen Receptor T cell therapies") is a therapy based on T cells expressing a chemical receptor for a specific antigen indicated for patients with some types of oncohematological pathologies that have not responded to other forms treatment, such as: relapsed or refractory non-Hodgkin's lymphomas, including diffuse large B-cell lymphoma, primary B-cell mediastinal lymphoma, transformed follicular lymphoma, mantle cell lymphoma, acute lymphoblastic leukemia, in children and young adults (<26 years) and multiple myeloma. This therapy is an absolutely innovative approach which consists of a personalized live cell immunotherapy that modifies the immune system of the recipient patient to make it able to recognize and eradicate the neoplastic cells expressing the antigen towards which the cells have been engineered.

This approach has several biological advantages:

  1. to supply the patient with "reprogrammed T cells" with a new and specific activation mechanism;
  2. overcoming immune tolerance towards cancer cells;
  3. bypassing HLA-mediated antigen recognition restriction mechanisms;

详细描述

The "CAR-T" immunotherapy ("Chimeric Antigen Receptor T cell therapies") is a therapy based on T cells expressing a chemical receptor for a specific antigen indicated for patients with some types of oncohematological pathologies that have not responded to other forms treatment, such as: relapsed or refractory non-Hodgkin's lymphomas, including diffuse large B-cell lymphoma, primary B-cell mediastinal lymphoma, transformed follicular lymphoma, mantle cell lymphoma, acute lymphoblastic leukemia, in children and young adults (<26 years) and multiple myeloma. This therapy is an absolutely innovative approach which consists of a personalized live cell immunotherapy that modifies the recipient patient's immune system to make it able to recognize and eradicate the neoplastic cells expressing the antigen towards which the cells have been engineered. CAR-T therapy uses specific immune cells (T lymphocytes) of the patient, isolated from his peripheral blood, engineered through the integration of genetic material encoding the chimeric receptor, expanded in vitro and then re-infused to activate the immune system response against the disease.

This approach has several biological advantages:

  1. to supply the patient with "reprogrammed T cells" with a new and specific activation mechanism;
  2. overcoming immune tolerance towards cancer cells;
  3. bypassing HLA-mediated antigen recognition restriction mechanisms; The CAR-T therapies that have obtained the Marketing Authorization (AIC) in the European Union and in Italy are: the drug Kymriah, drug Yescarta.

The therapeutic indications for which they have been approved are:

  • Kymriah (tisagenlecleucel): pediatric and young adult patients up to 25 years of age with B-cell acute lymphoblastic leukemia who have never responded to chemotherapy, or who have relapsed after allogeneic haematopoietic stem cell transplantation or after at least 2 lines chemotherapy; patients with diffuse large B cell lymphoma or DLBCL who have already undergone at least 2 lines of systemic therapy;
  • Yescarta (axicabtagene ciloleucel): patients with diffuse large B cell lymphoma or DLBCL, primary mediastinal B cell lymphoma or PMBCL who have already received at least 2 lines of systemic therapy. CAR-T therapies represent an important therapeutic option for the lymphoproliferative diseases listed above and have been studied in patients in whom previous standard strategies (chemotherapy and haematopoietic stem cell transplantation) have not proved effective.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged ≥ 18 years. Patients with haematological pathology admitted to be subjected to CAR-T Therapy at the Advanced Cell Therapy Program, IRCCS University Hospital of Bologna.
  • Patients who consent to participate in this study after signing informed consent.

排除标准

  • 未提供

结局指标

主要结局

Study of epigenetics

时间窗: 5 years

Study of epigenetics in peripheral blood samples taken from patients undergoing CAR-T therapy. In particular, the epigenetic analysis will be performed in the circulating leukocyte and extracellular fraction contained in the plasma nanovesicles in order to determine the epigenome and its correlation with the clinical outcome.

Study of microRNA

时间窗: 5 years

study of microRNAs extracted from extracellular vesicles and leukocytes of patients undergoing CAR-T therapy in order to correlate levels with clinical outcome.

study of lymphocyte and myeloid populations

时间窗: 5 years

study of lymphocyte and myeloid populations in the haematological patient PRE and POST CAR-T cell infusion in order to correlate the levels with the clinical outcome.

次要结局

未报告次要终点

研究者

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

Francesca Bonifazi, MD

Hematologist Doctor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

研究点 (1)

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