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Relapsed and/or Refractory Non-Hodgkin Lymphoma Study (COMBOSTAT)

2017年9月15日 更新者:The Methodist Hospital Research Institute

Phase II Study of Combination Vorinostat and Bortezomib in Patients With Relapsed and/or Refractory Non-Hodgkin Lymphoma

The purpose of this study is to determine the rate of response to the drugs bortezomib (Velcade) and vorinostat (Zolinza), when used in combination, in patients with relapsed (recurrent) and/or refractory (difficult to treat) non-Hodgkin Lymphoma, and to determine the safety and tolerability of this regimen.

研究概览

详细说明

More selective and less toxic therapeutic strategies are needed to improve cure rates and prolong survival in patients with relapsed and/or refractory non-Hodgkin Lymphoma.

Amongst the multiple new pathways recently studied two have emerged as potentially important targets for new agents in lymphoma. These include the ubiquitin proteasome pathway and the biochemical reactions that control histone acetylation. The first two agents in each class to have been studied in lymphomas are: bortezomib and vorinostat. Bortezomib has been granted FDA approval for the treatment of mantle cell lymphoma and has established activity in a variety of B-cell lymphomas including follicular, marginal zone and diffuse large B-cell lymphoma. Vorinostat or SAHA (suberoylanilide hydroxamic acid) has been FDA approved for the treatment of refractory cutaneous T-cell lymphomas and has also shown activity in other lymphomas.

Synergistic activity between vorinostat and bortezomib has been observed in different cell lines. The proposed study will be a phase II trial of the combination of vorinostat and bortezomib at the recommended dose-schedule in patients with recurrent and/or refractory lymphomas, indolent and aggressive, and B or T.

研究类型

介入性

阶段

  • 阶段2

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Histologically confirmed non-Hodgkin Lymphoma including small lymphocytic lymphoma, lymphoplasmacytic lymphoma, follicular center cell lymphoma, mantle cell lymphoma, marginal zone lymphoma, diffuse large B cell lymphoma, Burkitt's lymphoma, lymphoblastic lymphoma, anaplastic large cell lymphoma, nasal NK/T cell lymphoma, mycosis fungoides/Sezary syndrome, angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphomas not otherwise specified
  • Received 2 or > prior therapies, which may include hematopoietic cell transplant (HCT)
  • Received treatment with a nucleoside analog, or an alkylating agent, an anthracycline and/or in the case of B cell lymphomas, rituximab
  • Resistant disease to 2 regimens or resistant disease to at least 1 regimen after first relapse
  • Bi-dimensionally measurable disease documented within 30 days prior to enrollment. Bidimensionally measurable disease is defined as:

    • A lymph node or tumor mass that can be accurately measured in two dimensions by CT,MRI, medical photograph (skin or oral lesion), plain X-ray, PET scan or other conventional technique and a greatest diameter of 1 cm or >; or palpable lesions with both diameters > 2 cm (lesion measured in 2 largest perpendicular dimensions in millimeters)
    • For the purposes of this protocol, disease should be located in an area of no prior radiation therapy or a clear progression in an area that was previously irradiated
  • Adequate organ and marrow function obtained < or = to 14 days prior to enrollment as defined by a(n):

    • ANC > or = to 1,000/microliter
    • Platelet count > or = to 100,000/microliter, or > or = to 75,000/microliter if the bone marrow is involved
    • Hemoglobin level > or = to 9 g/dL
    • Total bilirubin < or = to 1.5 x institutional upper limit of normality (ULN).(If abnormal, direct bilirubin less than or equal to 1.5 x institutional ULN)
    • ALT or AST < or = to 2.5 x institutional ULN (< or = to 5 x institutional ULN if liver involvement with lymphoma)
    • Serum creatinine < or = to 1.5 x institutional ULN
  • Zubrod (ECOG) Performance Status of 0 or 1
  • Age > than or = to 18 years
  • Life expectancy > or = to 3 months as clinically determined by referring physician
  • Female patient is either post menopausal, free from menses for > 2 years, surgically sterilized or willing to use highly effective methods of contraception (i.e., a condom in conjunction with a diaphragm, or spermicidal jelly; or oral, injectable, or implanted birth control; or abstinence ) to prevent pregnancy throughout the study, starting with visit 1
  • Female patients of childbearing potential must have a negative serum pregnancy test (beta-HCG) within 72 hours of enrollment and should not be nursing due to the potential for congenital abnormalities and of harm to nursing infants due to this treatment regimen
  • Male patient agrees to use an adequate method of contraception (i.e., a condom if female partner uses a diaphragm, spermicidal jelly; or oral, injectable, or implanted birth control; or abstinence) for the duration of the study and for 12 weeks after the last dose
  • Patient must be able to swallow capsules
  • Signed and dated IRB/ethics committee-approved informed consent before any protocol specific screening procedures are performed
  • Both men and women of all races and ethnic groups are eligible for this trial

Exclusion Criteria:

  • Prior investigational therapy within 3 weeks of enrollment. Investigational therapy is defined as treatment that is not approved for any indication
  • CNS metastases, as indicated by clinical symptoms,cerebral edema, requirement for corticosteroids and/or progressive growth (treated CNS metastases must be stable for greater than 2 weeks prior to enrollment)
  • Active second malignancy that requires treatment or that would interfere with assessment of response
  • Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer with < 5 years of documented disease-free status
  • Treatment with the following within the timeframe specified prior to enrollment:

    • Chemotherapy, radiotherapy, immunotherapy (active (such as vaccines) or passive (such as monoclonal antibodies or immunotoxins)) or major surgery < or = to 3 weeks;
    • Nitrosourea, or mitomycin < or = to 6 weeks
    • Radioimmunotherapy (e.g. Bexxar or Zevalin) < or = to 12 weeks
    • Concurrent enzyme-inducing anticonvulsant agents or valproic acid in last 4 weeks
    • Prior bortezomib or any other proteasome inhibitor
    • Prior vorinostat or any other histone deacetylase inhibitor
    • Concurrent systemic corticosteroids (<10 mg/day of prednisone or equivalent for adrenal insufficiency or acute allergic reactions allowed)
  • Uncontrolled current illness including, but not limited to:

    • Clinically or laboratory determined active infection
    • Clinically limiting congestive heart failure or ejection fraction (EF) <45%
    • Clinically unstable angina pectoris (or myocardial infarction within 6 months of Day 1)
    • Clinically significant cardiac arrhythmia
    • Limiting pulmonary hypertension
    • Pre-existing neuropathy ≥ grade 2
    • Patients with pleural effusions, ascites or peripheral edema grade 2 or >
  • HIV
  • Active viral hepatitis
  • Major surgery or significant traumatic injury within 21 days prior to enrollment (this does not apply to placement of a venous access device)
  • Hypersensitivity to any of the components in vorinostat or bortezomib or agents containing boron or mannitol
  • Significant psychiatric illness/social situations that would limit compliance with study medication and requirements of the study as determined by study MD
  • Significant medical illness or abnormal laboratory finding that would, in the investigator's judgment, increase the subject's risk by participating in this study

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:非随机化
  • 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:Combination Vorinostat + Bortezomib
Six cycle combination therapy with vorinostat and bortezomib.
Patients will be treated with oral vorinostat on days 1 through 14 followed by a 7-day rest period, for a 21-day treatment cycle for up to 6 cycles in the absence of disease progression or unacceptable toxicity. The patients will receive once-daily oral vorinostat (400 mg) with bortezomib 1.3 mg/m2 as an IV push on days 1, 4, 8, 11.
其他名称:
  • vorinostat (Zolinza)
  • bortezomib (Velcade)

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Determine the response rate of this regimen in this patient population.
大体时间:6 cycles
6 cycles

次要结果测量

结果测量
大体时间
Determine the progression free survival of this regimen in this patient population.
大体时间:entire length of study
entire length of study
Determine the safety and tolerability of this regimen in this patient population.
大体时间:throughout course of study
throughout course of study
To correlate response rate and progression free survival with pre-treatment and post-treatment NFkB, TRAIL, cyclin D1, histone acetylation, EBV related proteins, and CTA expression.
大体时间:6 cycles
6 cycles

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。

调查人员

  • 首席研究员:Hector A Preti, M.D.、The Methodist Hospital Research Institute

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

2010年6月1日

初级完成 (实际的)

2012年5月1日

研究完成 (实际的)

2012年5月1日

研究注册日期

首次提交

2009年2月3日

首先提交符合 QC 标准的

2009年2月4日

首次发布 (估计)

2009年2月5日

研究记录更新

最后更新发布 (实际的)

2017年9月19日

上次提交的符合 QC 标准的更新

2017年9月15日

最后验证

2017年9月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

非霍奇金淋巴瘤的临床试验

Vorinostat in combination with Bortezomib的临床试验

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