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Epirubicin and Paclitaxel, Alone or Together With Capecitabine as First Line Treatment in Metastatic Breast Cancer (TEX)

2015年9月16日 更新者:Thomas Hatschek

Treatment With the Combination of Epirubicin and Paclitaxel Alone or Together With Capecitabine as First Line Treatment in Metastatic Breast Cancer. A Multicenter, Randomized Phase III Study

Anthracycline-taxane regimens are effective means of postponing progression in metastatic breast cancer. It is yet unclear whether addition of capecitabine to this combination improves the treatment outcome.

Patients with advanced breast cancer are randomized to first-line chemotherapy with a combination of epirubicin (Farmorubicin®) and paclitaxel (Taxol®) alone (ET) or in combination with capecitabine (Xeloda®, TEX). Starting doses for ET are epirubicin 75 mg/m2 plus paclitaxel 175 mg/m2, and for TEX epirubicin 75mg/m2, paclitaxel 155 mg/m2, and capecitabine 825 mg/m2 BID for 14 days. Subsequently, doses are tailored related to side effects.

Primary endpoint is progression-free survival (PFS); secondary endpoints are overall survival (OS), time to treatment failure (TTF), objective response (OR), safety and quality of life (QoL).

研究概览

研究类型

介入性

注册 (实际的)

304

阶段

  • 第三阶段

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

      • Göteborg、瑞典
        • Sahlgrenska University Hospital
      • Helsingborg、瑞典
        • Helsingborg Gen. Hospital
      • Kalmar、瑞典
        • Kalmar Central Hospital
      • Karlstad、瑞典
        • Karlstad Gen. Hospital
      • Linköping、瑞典
        • Linköping University Hospital
      • Lund、瑞典
        • Lund University Hospital
      • Malmö、瑞典
        • Malmö General University Hospital
      • Sundsvall、瑞典
        • Sundsvall Gen. Hospital
      • Umeå、瑞典
        • Norrland University 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

女性

描述

Inclusion Criteria:

  • Morphologically proven breast carcinoma
  • Written patient consent must be obtained
  • Measurable disease (i.e. at least one lesion that can be accurately measured in at least one dimension as ≥20 mm by conventional techniques, or as ≥10 mm by spiral CT scan) as defined in section 8.
  • Lytic and blastic bone metastases as only site of recurrence are allowed
  • Age 18 years or older
  • ECOG performance status 0-2
  • Life expectancy of at least three months
  • Adequate cardiac functions
  • Adequate hematological, renal and hepatic functions
  • Patient must be accessible for treatment and follow-up.

Exclusion Criteria:

  • Treatment-free interval less than one year, if previous adjuvant, neoadjuvant or after radically treated locoregional recurrence given regimen contained anthracycline, taxane or capecitabine. This limitation does not apply for regimens containing other than the drugs mentioned
  • During adjuvant treatment obtained cumulative doses exceeding 375 mg/m2 for doxorubicin, or 550 mg/m2 for epirubicin, abnormal ECG or reduced cardiac function measured by left ventricular ejection fraction (LVEF).
  • Indication for the use of trastuzumab (Herceptin) as first-line treatment in patients with tumor overexpressing c-erbB2.
  • Any previous chemotherapy for metastatic disease, except for radically treated locoregional relapse
  • Neoplasm other than breast carcinoma, except for non-melanoma skin cancer or curatively treated carcinoma in situ of the cervix, diagnosed during the past five years
  • Pregnancy or lactation
  • Known brain metastases
  • History of atrial or ventricular arrhythmias and/or congestive heart failure, even if medically controlled. History of clinical and electrocardiographically documented myocardial infarction
  • Preexisting motor or sensory neuropathy ≥ grade 2 according to NCI CTC 2.0 criteria (severe paresthesia and/or mild weakness, or worse)
  • Severe hepatic or renal impairment (for capecitabine: calculated creatinine clearance below 30 ml/min; for calculation, see p. 5.1.4) not allowing for adequate use of the proposed regimens
  • History of known dihydropyrimidine dehydrogenase (DPD) deficiency (severe reaction on previous treatment with fluorouracil, e.g experience of mucositis, hand-foot syndrome, or diarrhea)
  • Active infection or other serious underlying medical condition which would impair the ability of the patient to receive protocol treatment, including prior allergic reactions to drugs containing cremophor, such as teniposide, cyclosporin or vitamin K
  • Dementia or significantly altered mental status that would prohibit the understanding and giving of informed consent.

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: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
有源比较器:Epirubicin + paclitaxel (Taxol)
Epirubicin 75mg/m2 i.v., paclitaxel 175 mg/m2 i.v. on day 1 every 21 days.
75 mg/m2 i.v. every 3 weeks, both study arms
175 mg/m2 i.v., every 3 weeks study arm A 155 mg/m2 i.v., every 3 weeks study arm B
其他名称:
  • 紫杉醇
有源比较器:Paclitaxel + epirubicin + capecitabine
Paclitaxel 155 mg/m2 i.v., epirubicin 75 mg/m2 i.v day 1, capecitabine 1650 mg/m2 p.o. on days 1-14 every 21 days.
75 mg/m2 i.v. every 3 weeks, both study arms
175 mg/m2 i.v., every 3 weeks study arm A 155 mg/m2 i.v., every 3 weeks study arm B
其他名称:
  • 紫杉醇
1650 mg/m2 p.o. days 1-14 every 3 weeks study arm B
其他名称:
  • 希罗达

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
Time to progression
大体时间:From date of randomisation until date of first radiolocically documented progression or death from any cause, whichever comes first up to 78 months
Time to progression comparing treatment with ET vs. TEX in patients with advanced breast cancer. Evaluation every 9 weeks during treatment until progression as long as study treatment was given, and every 12 weeks until date of progression, if treatment was disrupted for any other reason. Patients in the state of persistent complete response after primary completion date were reported only upon date of progression or death up to 78 months
From date of randomisation until date of first radiolocically documented progression or death from any cause, whichever comes first up to 78 months

次要结果测量

结果测量
措施说明
大体时间
Time to treatment failure
大体时间:From date of randomization until date of treatment disruption for any reason up to 78 months
Time on treatment irrespective of reason for disruption (toxicity, patients wish)
From date of randomization until date of treatment disruption for any reason up to 78 months
Response rate
大体时间:Every 9 weeks during treatment
Every 9 weeks during treatment
Overall survival
大体时间:Time from randomisation until date of death up to 78 months
Date and cause of death reported yearly during the ongoing trial, up to 78 months after primary completion date only on the occasion of death
Time from randomisation until date of death up to 78 months
Number of participants with adverse events
大体时间:Continuously during treatment and until 2 months after termination
All side effects which appear during treatment are reported and graded according CTC v.2.
Continuously during treatment and until 2 months after termination
Quality of life
大体时间:Baseline, 2, 4, 6 and 9 months
Measured at five points during nine months from randomization.
Baseline, 2, 4, 6 and 9 months
Tumor biological data related to treatment
大体时间:Within two weeks before start of treatment
Fine needle aspirates from metastases
Within two weeks before start of treatment

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:Thomas Hatschek, PhD、Karolinska University 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。

一般刊物

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

2002年12月1日

初级完成 (实际的)

2006年6月1日

研究完成 (实际的)

2013年12月1日

研究注册日期

首次提交

2011年9月1日

首先提交符合 QC 标准的

2011年9月13日

首次发布 (估计)

2011年9月14日

研究记录更新

最后更新发布 (估计)

2015年9月17日

上次提交的符合 QC 标准的更新

2015年9月16日

最后验证

2015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.

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