NCT00496379终止2 期
A Phase 2 Study of ZK219477 (ZK-EPO) in Patients With Breast Cancer and Brain Metastases
适应症
干预措施
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Objective Response Rate in the Central Nervous System (CNS)
研究概览
简要总结
The purpose of this research study is to determine the effects (good and bad) of ZK219477(sagopilone) on participants and their cancer. ZK219477 is a chemotherapy drug that is thought to work by interfering with the ability of cancer cells to grow and divide. It is a part of a group of drugs called "epothilones" which appear to cause shrinkage of cancer in some patients with breast cancer. It is generally difficult for chemotherapy to enter the brain. However, it is believed that ZK219477 crosses into the brain. We are also studying whether an investigational MRI scan procedure may eventually help to predict which patients will benefit from ZK219477.
详细描述
- Participants will be given ZK219477 intravenously over approximately 30 minutes every three weeks.
- During all treatment cycles a physical exam and questions about the participants general health and specific questions about any problems they may be having will be performed.
- At least every three weeks blood tests will be done to assess the effect of ZK219477 on the body.
- After every 2 cycles of treatment, participants will have additional scans to assess the effect of ZK219477 on their cancer. This will include a CT scan of the abdomen, chest, and pelvis, and an MRI of the brain.
- At the time of the standard MRI, participants will be asked to undergo an additional MRI sequence, which means they will be in the MRI machine for approximately 15-20 more minutes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Patients must have histologically or cytologically invasive breast cancer, with metastatic disease at the time of screening
- •Measurable Central Nervous System (CNS) disease, as defined as at least one lesion > or equal too 10mm in longest dimension
- •New or progressive CNS lesions after at least one prior standard CNS-directed therapy for treatment of brain metastases, which could include surgical resection, whole brain radiotherapy (WBRT), and/or stereotactic radiosurgery (SRS). Patients must have received prior WBRT, SRS or both.
- •Patient has been evaluated by a radiation oncologist, who feels that the plan to evaluate systemic chemotherapy in place of additional brain radiotherapy is an acceptable option
- •No increase in corticosteroid use in the week prior to study entry
- •Any number prior lines of chemotherapy for metastatic breast cancer
- •18 years of age of older
- •Life expectancy of greater than 12 weeks
- •ECOG Performance Status 0-2
- •Patients must have normal organ function as outlined in the protocol
排除标准
- •Patients who have had chemotherapy within 3 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 3 weeks earlier
- •Patients who have had XRT within 3 weeks prior to entering the study or those who have not recovered from adverse events due to XRT
- •Patients may not be receiving any other investigational agent
- •Patients may not be receiving any cancer-directed therapy
- •Prior treatment with investigational chemotherapy for brain metastases
- •Prior treatment with epothilone for metastatic breast cancer
- •Leptomeningeal carcinomatosis as the only site of CNS involvement.
- •Concurrent treatment with an enzyme inducing antiepileptic drug, including phenytoin, carbamezepine, phenobarbital, or oxacarbazepine
- •More than 2 seizures over the last four weeks prior to study entry
- •Known contraindication to MRI or gadolinium contrast, such as cardiac pacemaker, ocular foreign body, or shrapnel
- •Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- •Pregnant or breastfeeding women.
研究组 & 干预措施
ZK219477
Experimental
干预措施: ZK219477 (Drug)
结局指标
主要结局
Objective Response Rate in the Central Nervous System (CNS)
时间窗: 2 years
Objective response rate is defined as at least a 50 percent reduction in the Central Nervous system target lesion volume compared to the lesion volume at baseline.
次要结局
- Time to Progression at Any Site.(2 years)
- Number of Subjects With Adverse Events (Any Grade)(2 years)
- Objective Response Rate in Non-Central Nervous System (CNS) Sites(2 years)
- Clinical Benefit Rate.(2 years)
研究者
Nancy Lin, MD
Assistant Professor of Medicine
Dana-Farber Cancer Institute
研究点 (1)
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