跳至主要内容
临床试验/NCT06626893
NCT06626893招募中不适用

Integrative "Omics" Approaches for Leukemia Target Identification and Matched Therapeutic Intervention

Azienda Ospedaliero-Universitaria di Parma8 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年3月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
8
主要终点
Frequencies of alternative therapies identified for AL patients

研究概览

简要总结

The goal of this clinical trial is to use multiple "omics" sciences to more thoroughly investigate Acute Recurrent/Refractory Leukemias (LA R/R) after conventional therapy in order to identify new targets and/or therapeutic approaches, in patients with a diagnosis of Acute Myeloid Leukemia (AML), Acute Lymphoblastic Leukemia/ Lymphoblastic Lymphoma B(ALL-B), Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma T (ALL-T), Acute Biphenotypic Leukemia/II as defined by WHO( World Health Organization) 2016, relapsed or refractory after at least one line of therapy. The main question that the trial aims to answer is: "Can molecules with known biological activity be active and represent possible new therapeutic strategies in relapsed/refractory Acute Leukemias on the basis of response profiles identified through the integration of next-generation chemogenomic and functional analyses? " It is expected that a minimum of 100 patients, male and female, aged 18 years and older, will be included. To participate in the study, the patient must consent to the performance on biological specimen (peripheral blood and bone marrow) of genetic/molecular and/or "omics" investigations performed with modern sequencing techniques, such as Next Generation Sequencing, Single Cell RNA Seq (scRNAseq), RT-qPCR(Quantitative reverse transcription polymerase chain reaction). These investigations will aim to improve the understanding of the genetic and molecular alterations of her disease. In addition, your cells will be used in the laboratory to perform in vitro sensitivity studies (drug response profiling - DRP) that aim to simultaneously test a set of hundreds of drugs to assess sensitivity or resistance profiles of your disease cells with the aim of identifying specific new therapies that target specific cellular mechanisms. In addition, part of the biological sample will be used for investigations of the bone marrow microenvironment and the "secretome", i.e., cell signaling molecules and methods. In order to accomplish this study, samples from peripheral or bone marrow blood taken during routine investigations performed during follow-up and re-evaluation visits for the patient's disease as per normal clinical practice will be used. Among the investigations that will be performed on the blood sample will be the genetic/molecular and/or omics and preclinical investigations described above.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

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

  • Patients to be enrolled in the study must have a diagnosis of AML, B ALL/LBL, T ALL/LBL, MPAL/AUL as described by WHO 2016 classification and must complained relapsed or refractory disease after at least one line of therapy
  • Ages Eligible for Study: over 18years
  • Patients must have greater than 5% blasts in the bone marrow with or without extramedullary disease
  • Patients with must have recurrent disease, documented by clinical or radiographic criteria, as well as histologic verification of the malignancy at original diagnosis
  • Patients may be enrolled on study regardless of the timing of prior I therapy
  • Patients must be capable of understanding the investigational nature and the objectives of the study. All patients must sign a written informed consent.

排除标准

  • 未提供

研究组 & 干预措施

Relapsed Refractory Acute Leukemias

Other

Functional and genomics analyses will be performed on primary sample from each enrolled patient (biological preclinical study)

干预措施: Functional tests (Biological)

Relapsed Refractory Acute Leukemias

Other

Functional and genomics analyses will be performed on primary sample from each enrolled patient (biological preclinical study)

干预措施: Next Generation Sequencing analysis (Genetic)

Relapsed Refractory Acute Leukemias

Other

Functional and genomics analyses will be performed on primary sample from each enrolled patient (biological preclinical study)

干预措施: Microvesicles analysis (Biological)

结局指标

主要结局

Frequencies of alternative therapies identified for AL patients

时间窗: 12 months

Number of patients treated with alternative therapies

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

Benedetta Cambò

MD, PhD

Azienda Ospedaliero-Universitaria di Parma

研究点 (8)

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