Erlotinib in Treating Patients With Advanced Non-Small Cell Lung Cancer
Multicenter Phase II Trial of OSI-774 (Erlotinib, Tarceva) in Patients With Advanced Bronchioalveolar Cell Lung Cancer.
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.
研究概览
详细说明
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.
OUTLINE: This is an open-label, nonrandomized, multicenter study.
Patients receive oral erlotinib hydrochloride daily in the absence of disease progression or unacceptable toxicity.
研究类型
注册 (实际的)
阶段
- 阶段2
联系人和位置
学习地点
-
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Illinois
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Chicago、Illinois、美国、60611
- Northwestern Memorial Hospital
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New York
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New York、New York、美国、10021
- Memorial Sloan-Kettering Cancer Center
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-
Tennessee
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Nashville、Tennessee、美国、37232
- Vanderbilt-Ingram Cancer Center
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-
Texas
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Houston、Texas、美国、77030
- MD Anderson Cancer Center
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
DISEASE CHARACTERISTICS:
Histologically confirmed bronchoalveolar cell (or a variant) non-small cell lung cancer (NSCLC)
- Stage IIIB (malignant pleural or pericardial effusion) disease
- Stage IV disease
- Recurrent and/or medically inoperable disease
- Measurable or evaluable indicator lesions
- No uncontrolled CNS metastases (i.e., any known CNS lesion that is radiographically unstable, symptomatic, and/or requiring escalating doses of corticosteroids)
PATIENT CHARACTERISTICS:
- ECOG performance status (PS) 0-1 OR Karnofsky PS 80-100%
- Life expectancy ≥ 8 weeks
- WBC ≥ 3,000/mm³
- Hemoglobin ≥ 9.0 g/dL
- Platelet count ≥ 100,000/mm³
- Bilirubin ≤ 1.0 mg/dL
- AST ≤ 2 times upper limit of normal
- Creatinine ≤ 1.5 mg/dL OR creatinine clearance ≥ 55 mL/min
- Not pregnant or nursing
- Fertile patients must use effective contraception
No significant medical history or unstable medical condition, including any of the following:
- Unstable systemic disease
- Congestive heart failure
- Recent myocardial infarction
- Unstable angina
- Active infection
- Uncontrolled hypertension
- No other active malignancies within the past 5 years except for adequately treated carcinoma of the cervix or basal cell or squamous cell skin cancer
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- At least 3 weeks since prior radiation therapy to a major bone marrow-containing area
- At least 3 weeks since prior chemotherapy
- No more than 1 prior chemotherapy regimen for NSCLC
- No prior systemic cytotoxic chemotherapy for other malignant diseases
- No prior erlotinib hydrochloride or other agents targeting the HER family (e.g., cetuximab, trastuzumab [Herceptin®], or gefitinib)
- No concurrent radiotherapy or chemotherapy
学习计划
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:Therapeutic Intervention
Patients will receive erlotinib (OSI-774) 150 mg daily by mouth.
If specified toxicities occurs, the dose may be reduced.
|
All patients will receive 150 mg orally daily
其他名称:
|
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 |
|---|---|---|
|
Major objective response rate (complete response and partial response)
大体时间: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
|
At 4 weeks and then every 8 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Worst grade toxicity
大体时间:weekly for 4 weeks, then every 8 weeks to discontinuation of drug
|
Number of patients with worst-grade toxicity at each of five grades (1 = mild, 2 = moderate, 3 = severe, 4 = life-threatening, disabling, 5 = death) following NCI Common Toxicity Criteria, v. 2. Drug is discontinued for disease progression, unacceptable toxicity, patient undergoes radiation or other chemotherapy, or withdraws from study
|
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
大体时间:baseline, every week for 5 weeks, and then every 4 weeks
|
The Lung Cancer Symptom Scale for patients is a nine-item scale with 0 = lowest rating (least) to 100 = highest rating (worst) for the measurement of symptom burden for loss of appetite, fatigue, cough, dyspnea, hemoptysis, activity, quality of life, lung cancer symptoms, and pain.
|
baseline, every week for 5 weeks, and then every 4 weeks
|
|
Survival
大体时间:from study entry to date of death or last date known alive
|
Duration of time from date of study entry to death from any cause or to the last date the patient is known to be alive.
|
from study entry to date of death or last date known alive
|
合作者和调查者
调查人员
- 首席研究员:William Pao, MD、Vanderbilt-Ingram Cancer Center
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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