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临床试验/NCT00984542
NCT00984542已完成2 期

Phase II Study of Second-Line Bendamustine in Relapsed or Refractory Small Cell Lung Cancer (SCLC).

Vanderbilt-Ingram Cancer Center6 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2009年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
50
试验地点
6
主要终点
Time to Progression

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as bendamustine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

PURPOSE: This phase II trial is studying how well bendamustine works as second- or third-line therapy in treating patients with relapsed or refractory small cell lung cancer.

详细描述

OBJECTIVES:

Primary

  • To determine the time to progression in patients with relapsed or refractory small cell lung cancer treated with second- or third-line bendamustine.

Secondary

  • To determine the toxicity of this drug in these patients.
  • To determine the response rate, progression-free survival, and overall survival of patients treated with this drug.

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
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Bendamustine

Experimental

干预措施: bendamustine hydrochloride (Drug)

结局指标

主要结局

Time to Progression

时间窗: On-study to date of progression, measured following cycle 2, 4, and 6 of a 21-day cycle for 6 cycles, (during 126 days)

Estimated probable duration from on-study date to date of disease progression, using the Kaplan-Meier method with censoring (see analysis population description for additional details). Disease progression is defined under RECIST v1.1 as \>=20% increase in sum of longest diameters of target lesions, unequivocal progression of non-target lesions, or appearance of new lesions.

次要结局

  • Number of Patients With Each Worst-grade Toxicity(Day 1 of each 21-day cycle for 6 cycles and at 30 days after end of treatment, at 156 days)
  • Best Response(On-treatment date to date of disease progression, following cycle 2, 4, and 6 of a 21-day cycle for 6 cycles, (assessed up to 126 days))
  • Progression-free Survival(On-study date to lesser of date of progression or date of death from any cause ,measured following cycle 2, 4, 6 of a 21-day cycle for 6 cycles, (assessed up to 126 days))
  • Overall Survival(On study to date of death from any cause or last date known alive, measured every 6-8 weeks from the end of treatment, up to 31 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Leora Horn, MD

Assistant Professor of Medicine; Assistant Director, Educator Development Program; Clinical Director, Thoracic Oncology Program; Medical Oncologist

Vanderbilt-Ingram Cancer Center

研究点 (6)

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