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Combination Chemotherapy in Treating Patients With Extensive-Stage Small Cell Lung Cancer

2014年1月8日 更新者:Case Comprehensive Cancer Center

An Open-Label, Multicenter, Randomized, Phase III Study Comparing Oral Topotecan/Cisplatin Versus Etoposide/Cisplatin As Treatment For Chemotherapy-Naive Patients With Extensive Disease - Small Cell Lung

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known which combination chemotherapy regimen is more effective in treating extensive-stage small cell lung cancer.

PURPOSE: Randomized phase III trial to compare different chemotherapy regimens in treating patients who have extensive-stage small cell lung cancer.

研究概览

详细说明

OBJECTIVES:

  • Compare the overall survival of patients with chemotherapy-naive extensive stage small cell lung cancer treated with cisplatin and oral topotecan vs cisplatin and etoposide.
  • Compare the response rates, response duration, and time to progression in patients treated with these regimens.
  • Compare the tolerability of these regimens in these patients.
  • Compare the patient-perceived disease status and well being in patients treated with these regimens.

OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to gender, ECOG performance status (0 vs 1 vs 2), lactate dehydrogenase (less than 1.5 times upper limit of normal (ULN) vs 1.5 times ULN or greater), and country. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral topotecan once daily on days 1-5 and cisplatin IV on day 5.
  • Arm II: Patients receive cisplatin IV on day 1 and etoposide IV over at least 30 minutes on days 1-3.

Treatment in both arms repeats every 21 days for at least 4 courses in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline, prior to each course, at 4 weeks after study, and then every 4 weeks for 16 weeks.

Patients are followed at 4 weeks, every 4 weeks for 16 weeks, and then every 3 months thereafter.

PROJECTED ACCRUAL: Approximately 760 patients (380 per treatment arm) will be accrued for this study within 18 months.

研究类型

介入性

注册 (实际的)

4

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

    • Ohio
      • Cleveland、Ohio、美国、44106-5065
        • Ireland Cancer 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

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed extensive stage small cell lung carcinoma (SCLC)
  • No prior chemotherapy for SCLC OR
  • No chemotherapy within 5 years of diagnosis of SCLC
  • Prior radiotherapy to measurable or nonmeasurable disease field allowed provided radiotherapy was completed at least 6 weeks ago and the disease is demonstrated to be progressing
  • No clinical signs or symptoms of brain and/or leptomeningeal metastases by CT scan or MRI

    • Brain and/or leptomeningeal metastases that are asymptomatic on neurologic exam are allowed provided metastases do not require corticosteroid therapy to control symptoms

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • ECOG 0-2

Life expectancy:

  • At least 3 months

Hematopoietic:

  • Hemoglobin at least 9.0 g/dL
  • WBC at least 3,500/mm3
  • Platelet count at least 100,000/mm3
  • Neutrophil count at least 1,500/mm3

Hepatic:

  • Bilirubin no greater than 2.0 mg/dL
  • SGOT and SGPT no greater than 2 times the upper limit of normal (ULN) (5 times ULN if liver metastases present)
  • Alkaline phosphatase no greater than 2 times ULN (5 times ULN if liver metastases present)

Renal:

  • Creatinine no greater than 1.5 mg/dL
  • Creatinine clearance at least 60 mL/min
  • No pre-existing renal impairment that would preclude cisplatin use

Gastrointestinal:

  • No clinical evidence of any gastrointestinal (GI) conditions including:

    • Removal of a portion of the stomach
    • History of recent obstruction of the GI tract
    • GI autonomic neuropathy
    • Ulcerative colitis
    • Crohn's disease
    • Malabsorption syndrome
    • Treatment with cyclosporine that would alter absorption or GI motility
  • No other conditions that would preclude absorption of oral topotecan

Other:

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception for 3 months prior to study, during, and for at least 1 month after study
  • No active infection
  • No other prior or concurrent malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or localized low-grade prostate cancer
  • No other concurrent severe medical problems that would expose the patient to extreme risk or preclude study compliance
  • No prior allergic reactions to compounds chemically related to study drugs
  • No pre-existing hearing impairment that would preclude cisplatin use
  • No overall medical condition for which study drugs would be inappropriate

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • No concurrent immunotherapy for SCLC

Chemotherapy:

  • See Disease Characteristics
  • No other concurrent chemotherapy for SCLC

Endocrine therapy:

  • See Disease Characteristics
  • No concurrent hormonal therapy for SCLC

Radiotherapy:

  • See Disease Characteristics
  • At least 24 hours since prior radiotherapy with no expected bone marrow suppression
  • Recovered from prior palliative radiotherapy (e.g, nausea and vomiting from radiation of the epigastrium)
  • No concurrent radiotherapy for SCLC
  • No concurrent radiotherapy for palliation of bone metastases or CNS lesions unless approved by the investigator

Surgery:

  • At least 3 weeks since prior major surgery (a shorter period is allowed if deemed in the best interest of the patient)

Other:

  • More than 30 days or 5 half-lives (whichever is longer) since prior investigational drugs
  • No other concurrent investigational therapy for SCLC
  • No concurrent cyclosporine
  • No concurrent drugs that would preclude absorption of oral topotecan

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:oral topotecan plus cisplatin IV
oral topotecan once daily on days 1-5 and cisplatin IV on day 5
实验性的:Cisplatin IV plus etoposide IV
Cisplatin IV on day 1 and etoposide IV over at least 30 minutes

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

  • 学习椅:Nathan Levitan, MD、Case Comprehensive Cancer Center

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

2001年9月1日

初级完成 (实际的)

2002年11月1日

研究完成 (实际的)

2002年11月1日

研究注册日期

首次提交

2002年7月8日

首先提交符合 QC 标准的

2003年1月26日

首次发布 (估计)

2003年1月27日

研究记录更新

最后更新发布 (估计)

2014年1月9日

上次提交的符合 QC 标准的更新

2014年1月8日

最后验证

2014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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