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An Expanded Cohort Trial of Bortezomib and Sorafenib in Advanced Malignant Melanoma

2016年6月7日 更新者:Ryan Sullivan, M.D.、Massachusetts General Hospital

A Phase I Expanded Cohort Trial of Bortezomib and Sorafenib in Advanced Malignant Melanoma

This research study involves the use of two investigational drugs: sorafenib and bortezomib. Sorafenib is designed to stop the growth of cells caused by changes associated with cancer. Bortezomib is designed to stop cancer cells from getting rid of waste products. This causes the cells to build up toxic levels of waste that leads to cell death. In the laboratory, the combination of sorafenib and bortezomib has been shown to fight cancer cells better than either drug alone. We are looking to determine if the combination of sorafenib and bortezomib is a safe treatment for patients with advanced melanoma. The effectiveness of this combination will also be assessed.

研究概览

地位

完全的

条件

详细说明

  • Since we are looking for the highest dose of the study drug that can be administered safely without severe or unmanageable side effects in participants that have melanoma, not everyone who participates will receive the same dose of the study drug. The dose participants will get will depend upon the number of participants who have been enrolled in the study before and how well they tolerated their doses.
  • Each treatment cycle lasts 28 days. Participants will take sorafenib orally twice a day and will receive bortezomib as an out-patient intravenous injection on Days 1, 8 and 15 of every cycle.
  • At the end of each treatment cycle, participants will be examined to determine whether their disease has worsened, improved or stayed the same, and to see if they are experiencing any side effects of treatment. The following tests will be done at these visits: physical examination, vital signs, blood tests and scans (repeated every 2 months).
  • Once the maximum tolerated dose of sorafenib and bortezomib have been determined, an additional 12 participants will be enrolled in this study. This is called the expansion cohort of this study. Participants enrolled in this cohort will be required to undergo a biopsy of the tumor lesion before they start study treatment and an additional biopsy after you start study treatment.

研究类型

介入性

注册 (实际的)

11

阶段

  • 阶段1

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

    • Massachusetts
      • Boston、Massachusetts、美国、02215
        • Beth Israel Deaconess Medical Center
      • Boston、Massachusetts、美国、02115
        • Dana-Farber Cancer Institute
      • Boston、Massachusetts、美国、02114
        • Massachusetts General Hospital

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:

  • Histological or cytological confirmation of malignant melanoma that is metastatic or unresectable
  • Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension as 10mm or greater with spiral CT scan
  • Patients may have received up to 4 prior treatments for their disease including immunotherapies such as high-dose interleukin 2 and antibodies directed against the human cytotoxic T-lymphocyte antigen 4
  • 18 years of age or older
  • Life expectancy of greater than three months
  • ECOG Performance status of 0 or 1
  • Adequate organ and marrow function as outlined in the protocol
  • Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment
  • INT < 1.5 or a PT/PTT within normal limits. Patients receiving anti-coagulation treatment wih an agent such as warfarin or heparin may be allowed to participate. For patients on warfarin, the INR should be measured prior to initiation of sorafenib and monitored at least weekly, or as defined by the local standard of care, until INR is stable
  • Women of child-bearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation.

Exclusion Criteria:

  • Chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events dur to agents administered more than 4 weeks earlier
  • Participants may not be receiving any other study agents
  • Known, active CNS disease, including primary brain tumor, seizures not controlled with standard medical therapy, any unstable or untreated brain metastasis, or history of stroke within the past 12 months
  • Prior therapy with bortezomib, sorafenib, or other proteasome inhibitor
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to sorafenib and bortezomib
  • Participants receiving any medications or substances that are inducers of CYP3A4
  • Known cardiac disease including congestive heart failure > class II NHYA, unstable angina or new onset angina, myocardial infarction within the past 6 months, or electrocardiographic evidence of acute ischemic or active conduction system abnormalities. Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant
  • Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy
  • Uncontrolled intercurrent illness
  • Pregnant women
  • Individuals with a history of a different malignancy are ineligible except for the circumstances outlined in the protocol
  • HIV-positive individuals on combination antiretroviral therapy
  • Uncontrolled hypertension despite optimal medical management
  • Thrombolic or embolic events
  • Pulmonary hemorrhage/bleeding event CTCAE Grade 2 or greater within 4 weeks of first dose of study drug
  • Any other hemorrhage/bleeding event CTCAE Grade 3 or greater within 4 weeks of first dose of study drug
  • Serious non-healing wound, ulcer or bone fracture
  • Evidence or history of bleeding diathesis or coagulopathy
  • Major surgery, open biopsy or significant traumatic injury within 4 weeks of first study drug
  • Any condition that impairs patient's ability to swallow whole pills
  • Any malabsorption problem
  • Known hypersensitivity to boron or mannitol
  • Grade 2 or greater peripheral neuropathy within 14 days before enrollment

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:剂量递增
Given intravenously on days 1, 8 and 15 of each 28 day cycle
400mg taken orally twice a day

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
Maximally tolerated dose
大体时间:2 years
To determine the maximally tolerated dose of weekly bortezomib in combination with 400mg twice daily sorafenib.
2 years
Document and summarize toxicities
大体时间:2 years
To document and summarize the toxicities of weekly bortezomib in combination with 400mg twice daily sorafenib
2 years

次要结果测量

结果测量
措施说明
大体时间
Anti-tumor activity
大体时间:2 years
To document the anti-tumor activity of weekly bortezomib in combination with sorafenib by describing the six-month progression free survival, one-year progression-free survival, and objective response rate.
2 years

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:Ryan J. Sullivan, MD、Massachusetts General Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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9月1日

初级完成 (实际的)

2013年2月1日

研究完成 (实际的)

2016年6月1日

研究注册日期

首次提交

2010年3月1日

首先提交符合 QC 标准的

2010年3月1日

首次发布 (估计)

2010年3月2日

研究记录更新

最后更新发布 (估计)

2016年6月8日

上次提交的符合 QC 标准的更新

2016年6月7日

最后验证

2013年1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.

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