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Cisplatin, Paclitaxel, and Everolimus in Treating Patients With Metastatic Breast Cancer

2013年3月7日 更新者:Ingrid Mayer, MD、Vanderbilt-Ingram Cancer Center

A Phase I Study of Cisplatin, Paclitaxel, and RAD001 Patients With Metastatic Breast Cancer

RATIONALE: Drugs used in chemotherapy, such as cisplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving more than one drug (combination chemotherapy) together with everolimus may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of cisplatin, paclitaxel, and everolimus when given together for the treatment of patients with metastatic breast cancer.

研究概览

详细说明

OBJECTIVES:

Primary

  • To establish the safety profile and the maximum tolerated dose of the combination of cisplatin, paclitaxel, and everolimus in patients with metastatic breast cancer.

Secondary

  • To explore the antitumor activity of this regimen, in terms of response rate and time to progression in these patients.

OUTLINE: This is a multicenter study.

Patients receive cisplatin intravenously (IV) over 1 hour and paclitaxel IV over 1 hour on days 1, 8, and 15. Patients receive oral everolimus on days 1, 8, 15, and 21. Courses repeat every 4 weeks in the absence of disease progression and unaccepted toxicity.

After completion of study therapy, patients are followed at 4 weeks.

研究类型

介入性

注册 (实际的)

18

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

    • Tennessee
      • Nashville、Tennessee、美国、37232-6838
        • Vanderbilt-Ingram Cancer Center
      • Nashville、Tennessee、美国、37064
        • Vanderbilt-Ingram Cancer Center - Cool Springs
      • Nashville、Tennessee、美国、37064
        • Vanderbilt-Ingram Cancer Center at Franklin
      • Nashville、Tennessee、美国、37203
        • Sarah Cannon Cancer Center at Centennial Medical 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:

DISEASE CHARACTERISTICS:

  • Histologically confirmed invasive mammary carcinoma

    • Stage IV disease
  • No locally recurrent breast cancer
  • Patients with HER2/neu overexpressing tumors must have received prior trastuzumab (Herceptin®) in first-line treatment of metastatic breast cancer
  • Patients with estrogen receptor- or progesterone receptor-expressing tumors must have received prior endocrine therapy (i.e., aromatase inhibitors, fulvestrant, tamoxifen, or ovarian ablation) in first-line treatment of metastatic breast cancer
  • No symptomatic brain metastases

    • Patients with a history of brain metastases must be clinically stable and not taking steroids or therapeutic anticonvulsants that are CYP3A4 modifiers
    • Patients with asymptomatic brain metastases on prophylactic convulsants that are CYP3A4 modifiers are not eligible
  • Hormone receptor status not specified

PATIENT CHARACTERISTICS:

  • Menopausal status not specified
  • ECOG performance status 0-1
  • Life expectancy ≥ 6 months
  • ANC ≥ 1000/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Creatinine ≤ 1.5 times upper limit of normal (ULN)
  • Bilirubin ≤ 1.5 times ULN (3 times ULN if liver metastasis present)
  • SGOT and SGPT ≤ 1.5 times ULN (3 times ULN if liver metastasis present)
  • Alkaline phosphatase ≤ 3 times ULN if liver metastasis present
  • Able to swallow and retain oral medication
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 3 months after completion of study treatment
  • Must be disease-free from prior invasive cancers for > 5 years with the exception of completely resected basal cell or squamous cell carcinoma of the skin or successfully treated cervical carcinoma in situ
  • No malabsorption syndrome, disease significantly affecting gastrointestinal function, or ulcerative colitis
  • No uncontrolled intercurrent illness including, but not limited to:

    • Ongoing or active infection requiring parenteral antibiotics
    • Impairment of lung function (i.e., chronic obstructive pulmonary disease or lung conditions requiring oxygen therapy)
    • Symptomatic New York Heart Association class III-IV congestive heart failure
    • Unstable angina pectoris, angioplasty, stenting, or myocardial infarction within the past 6 months
    • Uncontrolled hypertension (systolic blood pressure [BP] > 180 mm Hg or diastolic BP > 100 mm Hg)
    • Clinically significant cardiac arrhythmia (i.e., multifocal premature ventricular contractions, bigeminy, trigeminy, or ventricular tachycardia that is symptomatic or requires treatment)
    • Uncontrolled diabetes
    • Psychiatric illness/social situations that would preclude compliance with study requirements
  • No known history of uncontrolled or symptomatic neuropathy ≥ grade 2
  • No hypersensitivity to paclitaxel, or drugs using the vehicle Cremophor, Chinese hamster ovary cell products, or other recombinant human antibodies

Exclusion Criteria:

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • Recovered from all prior treatment
  • Must not have exceeded a total cumulative dose of life-time exposure of doxorubicin hydrochloride ≤ 360 mg/m² or epirubicin hydrochloride ≤ 640 mg/m²
  • At least 2 weeks since other prior investigational drugs
  • No prior resection of the stomach or small bowel
  • No more than 4 prior chemotherapy regimens in the metastatic setting

    • This restriction does not include endocrine therapies or single agent biologic therapies (i.e., trastuzumab)
  • Concurrent radiotherapy to painful bone metastases or areas of impending bone fracture allowed as long as radiotherapy is initiated prior to study entry
  • No concurrent trastuzumab
  • No concurrent endocrine therapy
  • No concurrent CYP3A4 modifiers
  • No concurrent herbal supplement
  • No other concurrent anticancer therapy (chemotherapy, radiotherapy, surgery, immunotherapy, hormonal therapy, or biological therapy)

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:治疗干预
  • Dose Level: -3 20mg/m2/week 3-6 patients
  • Dose Level: -2 20mg/m2/week 3-6 patients
  • Dose Level: -1 25mg/m2/week 3-6 patients
  • Dose Level: 1 25mg/m2/week 3-6 patients
  • Dose Level: 2 25mg/m2/week 3-6 patients
  • Dose Level: 3 25mg/m2/week 3-6 patients
其他名称:
  • 铂醇
  • Dose Level: -3 20mg/m2/week 3-6 patients
  • Dose Level: -2 20mg/m2/week 3-6 patients
  • Dose Level: -1 20mg/m2/week 3-6 patients
  • Dose Level: 1 20mg/m2/week 3-6 patients
  • Dose Level: 2 25mg/m2/week 3-6 patients
  • Dose Level: 3 30mg/m2/week 3-6 patients
其他名称:
  • RAD001
  • Dose Level: -3 65mg/m2/week 3-6 patients
  • Dose Level: -2 70mg/m2/week 3-6 patients
  • Dose Level: -1 70mg/m2/week 3-6 patients
  • Dose Level: 1 80mg/m2/week 3-6 patients
  • Dose Level: 2 80mg/m2/week 3-6 patients
  • Dose Level: 3 80mg/m2/week 3-6 patients
其他名称:
  • 紫杉醇

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
Safety profile and maximum tolerated dose
大体时间:At 4 weeks
The Maximum Tolerated Dose (MTD) will be the dose level at which fewer than 2 of 6 (or 33% of) patients experience dose limiting toxicity (DLT).
At 4 weeks

次要结果测量

结果测量
措施说明
大体时间
Antitumor activity
大体时间:Date of study entry to date of progression of disease
Cisplatin + Paclitaxel + RAD001 combination by determining response rates (RR) and time to progression (TTP) achieved with treatment
Date of study entry to date of progression of disease
Response rate
大体时间:at baseline and every 8 weeks to disease progression
at baseline and every 8 weeks to disease progression
Time to progression
大体时间:date of study entry to date of disease progression
date of study entry to date of disease progression

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

2008年5月1日

初级完成 (实际的)

2009年8月1日

研究完成 (实际的)

2010年12月1日

研究注册日期

首次提交

2008年5月18日

首先提交符合 QC 标准的

2008年5月18日

首次发布 (估计)

2008年5月20日

研究记录更新

最后更新发布 (估计)

2013年3月8日

上次提交的符合 QC 标准的更新

2013年3月7日

最后验证

2013年3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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