Disulfiram for Preventing Treatment Complications in Patients Undergoing CAR T-cell Therapy for Relapsed or Refractory Diffuse Large B-cell Lymphoma
A Single Center, Phase I/II Study of Disulfiram for the Prevention of Immunotoxicity in Patients Undergoing CAR T-Cell Therapy
This phase I/II trial tests the safety, best dose, and effectiveness of disulfiram for preventing treatment complications in patients with large B-cell lymphoma that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory) and who are undergoing chimeric antigen receptor (CAR) T-cell therapy. Two major complications of CAR T-cell therapy include cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). CRS results from inflammation in the body when the immune system responds too aggressively to the modified T cells working to attack cancer cells. ICANS is inflammation of the brain or nerves. CRS is most often a prelude to ICANS, and both of these toxicities currently require immunosuppression for treatment, which can inhibit CAR T-cell response. Disulfiram has been found to impact several biologic pathways that cause CRS. Disulfiram may be safe and effective for reducing the incidence and severity of reactions to CAR T-cell therapy without inhibiting CAR T-cell response.
研究概览
地位
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Tracey Churay
- 电话号码:1-800-865-1125
- 邮箱:tchuray@umich.edu
学习地点
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-
Michigan
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Ann Arbor、Michigan、美国、48109
- University of Michigan Rogel Cancer Center
-
接触:
- Tracey Churay
- 电话号码:800-865-1125
- 邮箱:tchuray@umich.edu
-
首席研究员:
- Marcus Geer
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Histologic diagnosis of relapsed/refractory large B-cell lymphoma
- >= 18 years of age at the time of signing informed consent (ICF)
- Understands and voluntarily signs the ICF prior to conduct of any study-related assessments or procedures
- Willing to adhere to the study visit schedule and other protocol requirements
- Willing/able to abstain from any drug/substance at risk for reaction with disulfiram for the duration of treatment
- Eastern Cooperative Oncology Group (ECOG) performance status =< 2
- Eligible for therapy with axicabtagene ciloleucel per institutional criteria
- Confirmation of a manufactured CAR T-cell product within clinical specifications for axicabtagene ciloleucel
- Females and males of childbearing potential must be willing to use effective methods of contraception from the time of informed consent until 12 months (female) or 4 months (males with female partners of reproductive potential) after the cyclophosphamide infusion
- Willingness to consent / co-enroll on the University of Michigan cellular therapy long-term follow-up study - HUM00043287 (UMCC2001-0234)
Exclusion Criteria:
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Serious or uncontrolled infection defined as not having cleared infection despite being on appropriate antimicrobial therapy for 5 days would be excluded. Also any infection which, in the opinion of the investigator, places the patient at an unacceptable risk for treatment-related complications, could impede the ability to safely administer therapy, or could interfere with evaluation of study intervention
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Active hepatitis B or C (latent hepatitis B will not be excluded), or HIV. Entecavir prophylaxis can be used for latent hepatitis B. A patient's viral load must be undetectable per quantitative polymerase chain reaction (PCR) and/or nucleic acid testing at screening
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Total bilirubin of >= 1.5 x upper limit of normal (ULN) unless attributed to Gilbert's syndrome or underlying primary malignancy. Patients with Gilbert syndrome or underlying primary malignancy involving the liver with total bilirubin >= 2.5 x ULN (or absolute total bilirubin >= 3 mg/dL) should be excluded. Aspartate aminotransferase (AST): >= 2.5 x ULN, alanine aminotransferase (ALT): >= 2.5 x ULN
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Active concurrent autoimmune disease requiring systemic immunosuppression
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Active primary or secondary central nervous system (CNS) lymphoma
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Active clinically relevant central nervous system disease including but not limited to:
- Seizures/Epilepsy
- Stroke or unstable neurologic deficits within the past 12 months prior to enrollment
- Cerebral edema
- Aphasia
- Severe brain injury
- Cerebellar disease
- Documented history of dementia as confirmed by neuropsychiatric testing
- Parkinson's disease
- Psychosis
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Any other significant medical condition (including neurological or psychiatric) which, in the opinion of the investigator, places the participant at an unacceptable risk for treatment-related complications, could interfere with the successful or safe delivery of therapy, or could interfere with evaluation of study intervention or interpretation of participant safety or study results. Including but not limited to:
- Diabetes with associated autonomic dysfunction
- Uncontrolled Hypothyroidism
- Chronic or acute nephritis
- Hepatic cirrhosis/insufficiency
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Pregnant or nursing females
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Current or previous treatment with any other agents explicitly for prophylaxis of CRS or ICANS, including corticosteroids and investigational agents during the study enrollment period. Corticosteroids given for disease treatment should have a washout of at least 5 half-lives prior to cell infusion. Use of prophylactic antiseizure medications is not contraindicated
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History of, or a concurrent, clinically significant illness, medical condition or laboratory abnormality that, in the investigator's opinion, could affect the conduct of the study
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Concurrent use of prohibited medications or substances at risk of precipitating a disulfiram reaction
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Hypersensitivity to disulfiram or to other thiuram derivatives used in pesticides and rubber vulcanization
学习计划
研究是如何设计的?
设计细节
- 主要用途:支持治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Supportive care (disulfiram)
Patients receive disulfiram PO QD on days -5 to +21. Patients receive cyclophosphamide IV and fludarabine IV on days -5 to -3 and then receive axi-cel IV on day 0. Patients also undergo CT or PET/CT at screening and follow-up and undergo collection of blood samples throughout the trial. |
Given IV
其他名称:
Undergo collection of blood samples
其他名称:
Undergo CT or PET/CT
其他名称:
Undergo PET/CT
其他名称:
Given IV
其他名称:
Given IV
其他名称:
Given PO
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Incidence of dose-limiting toxicities
大体时间:Within day +35 post-chimeric antigen receptor (CAR) T-cell therapy
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At the end of the trial, will report number of patients assigned to each dose, as well as the number of patients experiencing toxicity at each dose. |
Within day +35 post-chimeric antigen receptor (CAR) T-cell therapy
|
|
Proportion of patients that are alive and free from grade 2-4 cytokine release syndrome (CRS) with no intervening treatment of CRS
大体时间:Through day +28 post-CAR T-cell therapy
|
At the end of the trial, will report number of patients assigned to each dose, as well as the number of patients experiencing efficacy outcomes at each dose. |
Through day +28 post-CAR T-cell therapy
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Incidence of grade 2-4 CRS
大体时间:By day +28 post-CAR T-cell therapy
|
The occurrence of severe CRS will be considered binary, and the rate will be defined as number of patients with severe CRS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
|
Incidence of all-grade CRS
大体时间:By day +28 post-CAR T-cell therapy
|
The occurrence of CRS will be considered binary, and the rate will be defined as number of patients with CRS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
|
Incidence of all-grade immune effector cell associated neurotoxicity syndrome (ICANS)
大体时间:By day +28 post-CAR T-cell therapy
|
The occurrence of severe ICANS will be considered binary and the rate will be defined as number of patients with severe ICANS divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
|
Incidence of disulfiram-related grade 2 to 5 non-hematologic toxicity
大体时间:By day +28 post-CAR T-cell therapy
|
Will be assessed by Common Terminology Criteria for Adverse Events, version 5.0. The occurrence of drug related grade 2-5 non-hematologic toxicity with at least a 'possible' attribution to disulfiram will be considered binary, and the rate will be defined as number of patients experiencing toxicity divided by the number of evaluable patients. The rate will be reported along with the 95% exact binomial confidence interval. |
By day +28 post-CAR T-cell therapy
|
合作者和调查者
调查人员
- 首席研究员:Marcus Geer、University of Michigan Rogel Cancer Center
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- UMCC 2025.132
- NCI-2026-05448 (注册表标识符:CTRP (Clinical Trial Reporting Program))
- HUM00287270 (其他标识符:University of Michigan Rogel Cancer Center)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
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研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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