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Temozolomide as a Prophylaxis Against Brain Recurrence in Participants With Metastatic Breast Cancer (P05225 AM2) (STOP)

2017年5月18日 更新者:Merck Sharp & Dohme LLC

Temozolomide in Metastatic Breast Cancer Patients at High Risk of Brain Recurrence: Impact on the Incidence of Brain Metastases (STOP)

The purpose of this study is to determine whether temozolomide can be used as a prophylaxis against brain recurrence in participants with metastatic breast cancer.

研究概览

详细说明

Breast cancer is the second most common cause of brain metastases. Overall survival after the development of brain metastases tends to be poor (6-8 months). Over-expression of Human Epidermal Growth Factor Receptor 2 (HER-2/neu), negative estrogen receptor, and young age at diagnosis seem to be indicators of high risk for brain metastases. Temozolomide may be a good candidate for prophylactic chemotherapy because of its ability to cross the blood-brain-barrier, achieving high concentrations in the central nervous system (CNS).

研究类型

介入性

注册 (实际的)

6

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

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Diagnosis of metastatic breast cancer.
  • Participants must have completed first line of metastatic chemotherapy and have achieved complete or partial response or disease stability for at least 6 months from the first confirmation of disease stabilization.
  • No clinical sign of brain progression.
  • At least one of the following 3 conditions: HER2 +++, Young age (< 50 years), and/or estrogen receptor (ER)-/progesterone receptor (PgR)-
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤2.
  • Life expectancy ≥3 months.
  • Neutrophils ≥1.5 x 10^9/L, platelets ≥100 x 10^9/L, hemoglobin ≥9 g/dL, lymphocytes ≥1 x 10^9/L.
  • Bilirubin level either normal or <1.5 x ULN (upper limit of normal).
  • AST (aspartate aminotransferase) and ALT (alanine aminotransferase) ≤2.5 x ULN (≤5 x ULN if liver metastases are present).
  • Serum creatine <1.5 x ULN.
  • Effective contraception if the risk of conception exists.

Exclusion Criteria:

  • Concurrent chronic systemic immune therapy not indicated in the study protocol.
  • Any investigational agent(s) within 4 weeks prior to entry.
  • Participants that have completed 2nd, 3rd, or 4th line metastatic chemotherapy or participant in active chemotherapy treatment.
  • Clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months.
  • Acute or sub acute intestinal occlusion or history of inflammatory bowel disease.
  • Known Grade 3 or Grade 4 allergic reaction to any of the components of the treatment.
  • Known drug abuse/alcohol abuse.
  • Legal incapacity or limited legal capacity.
  • Medical or psychological condition which in the opinion of the investigator would not permit the participant to complete the study or sign meaningful informed consent.
  • Women who are pregnant or breastfeeding.
  • Any concurrent malignancy other than non-melanoma skin cancer, or carcinoma in situ of the cervix (participants with a previous malignancy but without evidence of disease for ≥5 years will be allowed to enter the trial).

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:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 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:替莫唑胺
Capsules to equal 75 mg/m^2, orally, daily for 6 weeks, in 3 eight-week cycles
无干预:观察性的

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
Percent of Participants With Recurrence of Brain Metastases
大体时间:1 Year
The analysis could not be performed due to low enrollment.
1 Year

次要结果测量

结果测量
措施说明
大体时间
Number of Days With Progression-free Survival (PFS)
大体时间:24, 38, and 52 weeks

PFS was defined as the time interval from randomization to objective tumor progression or death from any cause.

The analysis could not be performed due to low enrollment.

24, 38, and 52 weeks
Number of Days With Disease-free Survival (DFS)
大体时间:24, 38, and 52 weeks

DFS was defined as the time interval from randomization to any relapse (loco-regional, contra-lateral, and/or distant).

The analysis could not be performed due to low enrollment.

24, 38, and 52 weeks
Number of Days With Distant Disease-free Survival (DDFS)
大体时间:24, 38, and 52 weeks

DDFS was defined as the time interval from randomization to only distant metastases (for example, bone, visceral organ, brain).

The analysis could not be performed due to low enrollment.

24, 38, and 52 weeks
Number of Days With Brain Recurrence-free Survival (BRFS)
大体时间:24,38, and 52 weeks

BRFS was defined as the time interval from randomization to the appearance of brain metastases.

The analysis could not be performed due to low enrollment.

24,38, and 52 weeks
Number of Days on Temozolomide Treatment
大体时间:Baseline to 24 Weeks
This outcome measure was only applicable to the temozolomide arm; the observation arm was therefore not analyzed.
Baseline to 24 Weeks
Total Dose of Temozolomide Taken
大体时间:Baseline to 24 Weeks
This outcome measure was only applicable to the temozolomide arm; the observation arm was therefore not analyzed.
Baseline to 24 Weeks
Number of Participants Who Had at Least One Dose Reduction During Treatment
大体时间:Baseline to 24 Weeks
This outcome measure was only applicable to the temozolomide arm; the observation arm was therefore not analyzed.
Baseline to 24 Weeks
Number of Participants Who Had at Least One Treatment Omission During Treatment
大体时间:Baseline to 24 Weeks
This outcome measure was only applicable to the temozolomide arm; the observation arm was therefore not analyzed.
Baseline to 24 Weeks
Number of Participants Who Completed the Third Cycle of Treatment
大体时间:Baseline to 24 Weeks
This outcome measure was only applicable to the temozolomide arm; the observation arm was therefore not analyzed.
Baseline to 24 Weeks

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)

2008年10月2日

初级完成 (实际的)

2010年6月30日

研究完成 (实际的)

2010年6月30日

研究注册日期

首次提交

2008年1月10日

首先提交符合 QC 标准的

2008年3月18日

首次发布 (估计)

2008年3月19日

研究记录更新

最后更新发布 (实际的)

2017年6月14日

上次提交的符合 QC 标准的更新

2017年5月18日

最后验证

2017年5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)?

是的

IPD 计划说明

http://www.merck.com/clinical-trials/pdf/Merck%20Procedure%20on%20Clinical%20Trial%20Data%20Access%20Final_Updated%20July_9_2014.pdf

http://engagezone.msd.com/ds_documentation.php

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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