Hu8F4治疗晚期血液系统恶性肿瘤患者
Hu8F4 在晚期血液系统恶性肿瘤患者中的 I 期研究
This phase I trial studies the side effects and best dose of anti-PR1/HLA-A2 monoclonal antibody Hu8F4 (Hu8F4) in treating patients with malignancies related to the blood (hematologic). Monoclonal antibodies, such as Hu8F4, may interfere with the ability of cancer cells to grow and spread.
研究概览
地位
条件
详细说明
PRIMARY OBJECTIVES:
I. To determine the dose limiting toxicity (DLT) and minimum safe and biologically-effective dose of Hu8F4 when administered intravenously in patients with leukemia or myelodysplastic syndrome (MDS).
II. To determine the pharmacokinetics (PK) of Hu8F4 following study drug administration.
SECONDARY OBJECTIVES:
I. To observe the anti-leukemia effects of Hu8F4 in patients with leukemias and MDS.
II. To measure the overall survival, disease-free survival and event-free survival of patients with leukemias or MDS treated with Hu8F4.
OUTLINE: This is a dose-escalation study.
Patients receive anti-PR1/HLA-A2 monoclonal antibody Hu8F4 intravenously (IV) over 60 minutes on days 1 and 15. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.
研究类型
注册 (实际的)
阶段
- 阶段1
联系人和位置
学习地点
-
-
Georgia
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Augusta、Georgia、美国、30912
- Augusta University
-
-
New York
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The Bronx、New York、美国、10467
- Montefiore Medical Center, Albert Einstein College of Medicine
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Texas
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Houston、Texas、美国、77030
- M D Anderson Cancer Center
-
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Utah
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Salt Lake City、Utah、美国、84112
- Huntsman Cancer Institute
-
-
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:
- Patients with any of the following diagnoses are eligible: 1) high-risk MDS (i.e. refractory anemia with excess blasts [RAEB-1 or RAEB-2] by World Health Organization [WHO] classification, or any WHO subset with International Prognostic Scoring System [IPSS] intermediate-2 or high, or any patients that have failed prior therapy with hypomethylating agents); 2) chronic myelomonocytic leukemia (CMML); 3) acute myeloid leukemia (AML) by WHO classification; 4) chronic myeloid leukemia in blast phase (CML-BP); 5) myelofibrosis with high-risk features (e.g., accelerated phase disease -10-19% blasts in peripheral blood or bone marrow-, or with Dynamic International Prognostic Scoring System [DIPSS]-plus high risk score)
- Patients must have relapsed/refractory disease and have failed, or are not candidates for, or have declined all available therapies of proven efficacy; they should also not be eligible for at the time of enrollment or have declined hematopoietic stem cell transplantation
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- The effects of Hu8F4 on a fetus or nursing child are unknown; women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) must use acceptable contraceptive methods (abstinence, intrauterine device [IUD], oral contraceptive or double barrier device), and must have a negative urine pregnancy test within 2 weeks prior to beginning treatment on this trial; nursing patients are excluded; sexually active men must also use acceptable contraceptive methods for the duration of time on study
- Patients must have human leukocyte antigen (HLA)-A2 phenotype
- Must be able and willing to give written informed consent
- Patients must be at least 2 weeks from prior chemotherapy, radiation therapy, or major surgery, and at least 4 weeks or 5 half lives from other investigational anticancer therapy, and have recovered from prior toxicities at least to grade 1; the exception is hydroxyurea that requires no washout prior to the start of study drug
- Clinically significant toxicities from prior chemotherapy must not be greater than grade 1
- Clearance creatinine or glomerular filtration rate (GFR) >= 40 mL/min
- Total bilirubin =< 1.5 x the upper limit of normal unless considered due to Gilbert's syndrome or leukemic involvement
- Alanine aminotransferase (ALT) =< 3 x the upper limit of normal unless considered due to leukemic involvement
Exclusion Criteria:
- Uncontrolled intercurrent illness including, but not limited to uncontrolled infection (patients must have no temperature >= 38.3 degrees Celsius [C] due to infection for at least 48 hrs to consider an infection controlled), psychiatric illness that would limit compliance with study requirements, or active heart disease including confirmed myocardial infarction within previous 3 months, symptomatic coronary artery disease, clinically significant arrhythmias not controlled by medication, or uncontrolled congestive heart failure New York (NY) Heart Association class III or IV
- Patients with current active malignancies or any remission for < 18 months, except patients with carcinoma in situ or with non-melanoma skin cancer who may have active disease or be in remission for less than 6 months
- Patients receiving any other standard or investigational treatment for their hematologic malignancy other than supportive care
- Patients who have had any major surgical procedure within 14 days of day 1
- Patients with known central nervous system infiltration with leukemia
- Patients who received an allogeneic stem cell transplant =< 90 days from the start of therapy
- Patients with active >= grade 3 graft versus host disease (GVHD), or receiving systemic steroids (> 10 mg/day of prednisone or equivalent) for GVHD
- Patients with known active central nervous system (CNS) disease; patients with history of active CNS disease should have at least two negative spinal fluid evaluations before being considered eligible
学习计划
研究是如何设计的?
设计细节
- 主要用途: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:Treatment (Hu8F4)
Patients receive anti-PR1/HLA-A2 monoclonal antibody Hu8F4 IV over 60 minutes on days 1 and 15. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. |
Correlative studies Correlative studies Given IV
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 |
|---|---|---|
|
Minimum safety data
大体时间:4 weeks
|
Safety data will be summarized using frequency and percentage for all patients. |
4 weeks
|
|
Biologically-effective dose
大体时间:4 weeks
|
Safety data will be summarized using frequency and percentage for all patients. |
4 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Overall survival
大体时间:Up to 4 years
|
Estimated using the Kaplan-Meier methods. |
Up to 4 years
|
|
Disease-free survival
大体时间:Up to 4 years
|
Estimated using the Kaplan-Meier methods. |
Up to 4 years
|
|
Event-free survival
大体时间:Up to 4 years
|
Estimated using the Kaplan-Meier methods. |
Up to 4 years
|
|
Duration of complete remission
大体时间:Up to 4 years
|
Complete remission rates will be estimated along with 95% credible intervals. Estimated using the Kaplan-Meier methods. |
Up to 4 years
|
合作者和调查者
调查人员
- 首席研究员:Tapan M Kadia、M.D. Anderson Cancer Center
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计的)
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
- 2014-0057
- P50CA100632 (美国 NIH 拨款/合同)
- 2014-0057 (其他标识符:M D Anderson Cancer Center)
- NCI-2015-02131 (其他标识符:NCI-CTRP Clinical Trials Reporting Registration)
- P-TRP-2447-14
- NCI-2015-02131 (注册表标识符:CTRP (Clinical Trial Reporting Program))
药物和器械信息、研究文件
研究美国 FDA 监管的药品
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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