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Azacitidine and Lenalidomide for Relapsed and Refractory Patients With Acute Myeloid Leukemia

2019年9月20日 更新者:University of Colorado, Denver

Sequential Treatment With Azacitidine and Lenalidomide for Relapsed and Refractory Patients With Acute Myeloid Leukemia

The primary objective of this study is to determine the complete remission/complete remission with incomplete recovery of blood counts (CR/CRi) rate for relapsed and refractory acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS) patients.

研究概览

详细说明

AML patients with relapsed and refractory disease have very poor outcomes. Sequential azacitidine and lenalidomide was recently shown by the PI of this study to be well-tolerated and effective in elderly, treatment naïve AML patients. Observations from this study and others that have piloted this combination have suggested that patients who received and failed prior treatments may also respond to this regimen. Therefore, the sequential combination of azacitidine with lenalidomide could potentially improve outcomes for relapsed and refractory AML patients by providing them with a treatment option that is tolerable and potentially clinically synergistic. To determine the efficacy of this combination in this population, we will pilot this phase 2 study.

研究类型

介入性

注册 (实际的)

37

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Colorado
      • Aurora、Colorado、美国、80045
        • University of Colorado Cancer Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • • World Health Organization (WHO)-confirmed AML, other than Acute Promyelocytic Leukemia (APL)

    • Age >18 years
    • White blood cell count (WBC) at initiation of treatment ≤ 10,000/L

      o If WBC is > 10,000/L patients may be started on an appropriate dose of hydroxyurea (to be determined by the investigators), until WBC < 10,000/L, at which time the hydroxyurea will be discontinued for 12 hours prior to enrollment

    • Relapsed or refractory (resistant) disease, as defined by standard criteria21:

      • Relapsed: Bone marrow blasts ≥5%; reappearance of blasts in the blood; development of extramedullary disease
      • Refractory (resistant): Failure to achieve Complete Remission (CR) or complete remission with incomplete recovery of blood counts (CRi) in patients who survive ≥7 days following completion of initial treatment, with evidence of persistent leukemia by blood and/or bone marrow examination
    • Failure of at least one prior therapy
    • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (See Appendix D: ECOG Performance Status Scale)
    • Life expectancy > 2 months
    • All study participants must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist® (RevAssist is a restricted distribution program for receiving lenalidomide)
    • Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 million International Units per milliliter (mIU/mL) 10 - 14 days prior to study enrollment and again within 24 hours of prescribing lenalidomide (prescriptions must be filled within 7 days) and must either commit to continued abstinence from heterosexual intercourse or begin two acceptable methods of birth control, one highly effective method and one additional effective method at the same time, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. See Appendix F: Risks of Fetal Exposure, Pregnancy Testing Guidelines and Acceptable Birth Control Methods
    • Willing and able to understand and voluntarily sign a written informed consent
    • Able to adhere to the study visit schedule and other protocol requirements

Exclusion Criteria:

  • • Known or suspected hypersensitivity to azacitidine or mannitol

    • Patients with advanced malignant hepatic tumors.
    • Treatment less than four weeks prior to enrollment with other experimental therapies or antineoplastic agents, with the exception of hydroxyurea
    • Inability to swallow or absorb drug
    • Prior treatment with lenalidomide for AML
    • Active opportunistic infection or treatment for opportunistic infection within four weeks of first day of study drug dosing
    • New York Heart Association Class III or IV heart failure
    • Unstable angina pectoris
    • Significant uncontrolled cardiac arrhythmias
    • Uncontrolled psychiatric illness that would limit compliance with requirements
    • Known Human immunodeficiency virus (HIV) infection
    • Graft vs. host disease ≥ grade 2
    • Relapse after allogeneic stem cell transplantation prior to post-transplant day 30
    • Pregnant or breast feeding females; lactating females must agree not to breast feed while taking lenalidomide
    • Other medical or psychiatric illness or organ dysfunction or laboratory abnormality which in the opinion of the investigator would compromise the patient's safety or interfere with data interpretation
    • Laboratory abnormalities:

      • Either creatinine >2.0 mg/dL or creatinine clearance <30 mL/min
      • Total bilirubin > 2 x institutional upper limit of normal (ULN) (unless documented Gilbert's syndrome)
      • Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) > 3 x institutional ULN

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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:Azacitidine + Lenalidomide + Off Therapy
Patients will receive 7 days of azacitidine followed by 3 weeks of lenalidomide. They will then have 2 weeks off therapy, for a maximum of 12 cycles.
Enrolled patients will receive 75 mg/m2 of azacitidine subcutaneously (SC) or intravenously (IV) on days 1-7 alone.
其他名称:
  • 维达扎 (TM)
Beginning on day 8, patients will receive 50 mg of lenalidomide PO, and will take this daily from day 8 through 28.
其他名称:
  • Revlimid (TM)
2 weeks off therapy, then begin sequence again for 12 weeks.

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
Percentage of Participants With Complete Remission or Complete Remission With Incomplete Recovery Blood Counts
大体时间:Interim assessment after 18 patients (estimated 2 years) and full assessment after 37 patients (estimated 3-4 years)
Change in baseline to end of study. To be assessed by standard criteria based on bone marrow examination. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR
Interim assessment after 18 patients (estimated 2 years) and full assessment after 37 patients (estimated 3-4 years)
Overall Response Rate
大体时间:Planned assessment after enrollment of all 37 patients (estimated 3-4 years)
Change in baseline to end of study. To be assessed by standard criteria based on bone marrow examination
Planned assessment after enrollment of all 37 patients (estimated 3-4 years)

次要结果测量

结果测量
措施说明
大体时间
Response or Remission Duration
大体时间:Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
Change in baseline to end of study. To be assessed by standard criteria based on bone marrow examination
Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
Toxicity and SAEs Related to Treatment
大体时间:Will begin assessment with first patient and will continue until completion of study, estimated to be 4 years
Change in baseline to end of study. To be measured based on Common Terminology Criteria for Adverse Events (CTCAE) criteria
Will begin assessment with first patient and will continue until completion of study, estimated to be 4 years
Overall Survival
大体时间:Depending on outcomes, will begin assessment at 2 years and will continue until completion of study, estimated to be at four years
Change in baseline to end of study
Depending on outcomes, will begin assessment at 2 years and will continue until completion of study, estimated to be at four years
Progression-free Survival
大体时间:Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
Change in baseline to end of study. To be assessed by standard criteria based on bone marrow examination
Depending on outcomes, will initiate this assessment after 2 years and will continue until completion of study, estimated at 4 years
Determine Biomarkers That Predict Response/Toxicity
大体时间:Three years after initiating study
Change in baseline to end of study. Planned assessments of methylation changes and other biomarkers. Computational biology modeling used to identify biomarkers and predict response.
Three years after initiating study

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2012年12月6日

初级完成 (实际的)

2016年4月27日

研究完成 (实际的)

2016年8月3日

研究注册日期

首次提交

2012年11月16日

首先提交符合 QC 标准的

2012年12月4日

首次发布 (估计)

2012年12月6日

研究记录更新

最后更新发布 (实际的)

2019年10月8日

上次提交的符合 QC 标准的更新

2019年9月20日

最后验证

2019年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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