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临床试验/NCT00416650
NCT00416650已完成2 期

Multicenter Phase II Trial of OSI-774 (Erlotinib, Tarceva) in Patients With Advanced Bronchioalveolar Cell Lung Cancer.

Vanderbilt-Ingram Cancer Center4 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2002年7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
16
试验地点
4
主要终点
Major objective response rate (complete response and partial response)

研究概览

简要总结

RATIONALE: Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

PURPOSE: This phase II trial is studying how well erlotinib works in treating patients with advanced non-small cell lung cancer.

详细描述

OBJECTIVES:

Primary

  • Determine the major objective response rate (partial response and complete response) in patients with advanced bronchoalveolar cell non-small cell lung cancer treated with erlotinib hydrochloride.

Secondary

  • Assess the quality of life of patients treated with this regimen.
  • Determine the duration of response and time to disease progression in patients treated with this regimen.
  • Determine the median survival of patients treated with this regimen.

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

Therapeutic Intervention

Experimental

Patients will receive erlotinib (OSI-774) 150 mg daily by mouth. If specified toxicities occurs, the dose may be reduced.

干预措施: erlotinib hydrochloride (Drug)

结局指标

主要结局

Major objective response rate (complete response and partial response)

时间窗: At 4 weeks and then every 8 weeks

Per Response Evaluation in Solid Tumors (RECIST) criteria v. 1.1: measurable lesions: complete response (CR) disappearance of target lesions, partial response (PR) \> 30% decrease in the sum of the longest diameter (LD) of target lesions

次要结局

  • Worst grade toxicity(weekly for 4 weeks, then every 8 weeks to discontinuation of drug)
  • Quality of life as measured by the Lung Cancer Symptom Scale for patients(baseline, every week for 5 weeks, and then every 4 weeks)
  • Survival(from study entry to date of death or last date known alive)

研究者

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

William Pao, MD

Professor of Medicine, Cancer Biology, & Pathology/ Microbiology/ Immunology; Director, Division of Hematology and Oncology; Ingram Professor of Cancer Research; Director, Personalized Cancer Medicine; Medical Oncologist

Vanderbilt-Ingram Cancer Center

研究点 (4)

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