Phase I Clinical Trial of AntiCD19 Chimeric Antigen Receptor T Cells for Treatment of Relapsed or Refractory Non Hodgkin Lymphoma
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 31
- 试验地点
- 2
- 主要终点
- Number of patients with Lymphoma response
研究概览
简要总结
The purpose of this study is to determine if it is possible to treat your cancer with a new type of T cell-based immunotherapy (therapy that uses your immune system to treat the cancer). T cells are a type of white blood cell that helps the body fight infections. This treatment uses T cells already present within your body that have been modified outside of the body and returned to target your cancer. This type of treatment is sometimes referred to as adoptive cell transfer (ACT). In this study the specific type of cells that will be used is called chimeric antigen receptor T cells (CAR T cells). Another purpose of this study is to learn about the side effects and toxicities related to this treatment.
详细描述
Primary Objective: To determine the safety of the treatment of relapsed or refractory B cell lymphomas with chimeric antigen receptor T cells targeting cluster of differentiation antigen 19 (CD19) and to find the recommended phase II dose for this cellular therapy
Secondary Objectives
- To describe the safety profile of the infusion of CAR-T cells targeting CD19.
- To describe the toxicities related to infusion of CAR-T cells targeting CD19.
- To describe the overall response rate and complete response rate of relapsed B cell malignancies treated with CAR-T cells targeting CD19.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 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
- 否
入选标准
- •Subjects must have relapsed or refractory non-Hodgkin lymphoma treated with at least two lines of therapy. Disease must have either progressed after the last regimen or presented failure to achieve partial or complete remission with the last regimen.
- •The patient's lymphoma must be CD19 positive, either by immunohistochemistry or flow cytometry analysis on the last biopsy available.
- •Eastern Cooperative Oncology Group (ECOG) Performance status ≤ 2
- •Total bilirubin ≤ 1.5 times the institutional upper limit of normal
- •Aspartate transaminase (AST or SGOT) ≤ 3 X institutional upper limit of normal
- •Alanine transaminase (ALT or SGPT) ≤ 3 X institutional upper limit of normal
- •Serum Creatinine ≤ 2 X the institutional upper limit of normal
- •Subjects must have the following hematologic function parameters:
- •absolute neutrophil count (ANC)>1,000/uL
- •Absolute Lymphocyte Count >100/uL
- •Platelets >50,000/uL
- •Subjects must have the ability to understand and the willingness to sign a written informed consent document.
排除标准
- •Autologous transplant within 6 weeks of planned CAR-T cell infusion
- •History of allogeneic stem cell transplant.
- •Recipient of CAR-T cell therapy outside of this protocol.
- •Active central nervous system or meningeal involvement by lymphoma. Subjects with untreated brain metastases or central nervous system (CNS) disease will be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events. Patients with a history of CNS or meningeal involvement must be in a documented remission by cerebrospinal fluid evaluation and contrast-enhanced MRI imaging for at least 90 days prior to registration.
- •Active malignancy, other than non-melanoma skin cancer, carcinoma in situ (e.g. cervix, bladder, breast).
- •HIV seropositivity
- •Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, pulmonary abnormalities or psychiatric illness/social situations that would limit compliance with study requirements.
- •Pregnant or breastfeeding women are excluded from this study because CAR-T cell therapy may be associated with the potential for teratogenic or abortifacient effects. Women of child bearing potential must have a negative serum pregnancy test. Because there is an unknown, but potential risk for adverse events in nursing infants secondary to treatment of the mother with CAR-T cells, breastfeeding should be discontinued. These potential risks may also apply to other agents used in this study.
- •Evidence of myelodysplasia or cytogenetic abnormality indicative of myelodysplasia on any bone marrow biopsy prior to initiation of therapy
- •Serologic status reflecting active hepatitis B or C infection. Patients that are positive for hepatitis B core antibody, hepatitis B surface antigen (HBsAg), or hepatitis C antibody must have a negative polymerase chain reaction (PCR) prior to enrollment. (PCR positive patients will be excluded.)
- •Patients with history of clinically relevant CNS pathology such as epilepsy, seizure disorders, paresis, aphasia, uncontrolled cerebrovascular disease, severe brain injuries, dementia and Parkinson's disease.
- •History of autoimmune disease (i.e. rheumatoid arthritis, systemic lupus erythematosus) with requirement of immunosuppressive medication within 6 months.
研究组 & 干预措施
Cyclophosphamide + Fludarabine + Infusion of CAR-T Cells
Lymphodepletive regimen, consisting of Cyclophosphamide 60mg/kg IV on day -6 and Fludarabine 25mg/m2 IV on days -5 to -3. Followed by infusion of Chimeric antigen receptor T-cells (CAR-T) on day 0
干预措施: Cyclophosphamide (Drug)
Cyclophosphamide + Fludarabine + Infusion of CAR-T Cells
Lymphodepletive regimen, consisting of Cyclophosphamide 60mg/kg IV on day -6 and Fludarabine 25mg/m2 IV on days -5 to -3. Followed by infusion of Chimeric antigen receptor T-cells (CAR-T) on day 0
干预措施: Fludarabine (Drug)
Cyclophosphamide + Fludarabine + Infusion of CAR-T Cells
Lymphodepletive regimen, consisting of Cyclophosphamide 60mg/kg IV on day -6 and Fludarabine 25mg/m2 IV on days -5 to -3. Followed by infusion of Chimeric antigen receptor T-cells (CAR-T) on day 0
干预措施: CAR-T Cells (Biological)
结局指标
主要结局
Number of patients with Lymphoma response
时间窗: Up to 12 months after getting CAR-T infusion
The 2014 Lugano Response for Malignant Lymphoma will be used the following categories of response: : Complete Response (CR), Partial Response (PR), Stable Disease (SD), Relapse and Progression (PD).
次要结局
- Duration of response(Up to 12 months after getting CAR-T infusion)
- Time to progression(Up to 12 months after getting CAR-T infusion)
- Time to treatment failure(Up to 12 months after getting CAR-T infusion)
- Disease-specific survival(Up to 12 months after getting CAR-T infusion)
- Progression-free survival(Up to 12 months after getting CAR-T infusion)
- Disease-free survival(Up to 12 months after getting CAR-T infusion)
研究者
Benjamin Tomlinson
Principal Investigator
Case Comprehensive Cancer Center