此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

PK Trial of Sorafenib & Erlotinib in Patients With Refractory Solid Tumors

2014年7月1日 更新者:SCRI Development Innovations, LLC

Pharmacokinetic Trial of Sorafenib and Erlotinib in Patients With Refractory Solid Tumors

Two cohorts of patients will be enrolled: Cohort A will consist of patients who are current smokers, and Cohort B will consist of patients who are current nonsmokers. There will be 24 patients enrolled in each cohort. Nonsmokers are patients who have not consumed tobacco or nicotine-containing products for 1 year before the start of the study. Patients classified as current smokers must have smoked a minimum of 10 cigarettes per day for up to 1 year. Patients who have smoked 1-9 cigarettes per day for up to 1 year, or more than 10 cigarettes per day for less than 1 year will not be eligible for this study.

研究概览

详细说明

Compared with supportive care alone, erlotinib has been associated with improved overall survival in patients with Refractory Solid Tumors; however, this absolute benefit is limited for the majority of patients. Incorporating other biologic agents into the second- or third-line treatment setting may prove to be a successful strategy in improving treatment efficacy (which has been recently demonstrated in several tumor types). Additionally, recent data suggest that smoking may influence the pharmacokinetic (PK) profile of erlotinib by increasing the metabolic clearance. Data suggest that the geometric mean erlotinib AUC(0-inf) and C(24h) are significantly decreased in smokers compared with nonsmokers (Hamilton et al. 2006). For this reason, this trial will enroll separate cohorts of patients who are current smokers and patients who are nonsmokers. Nonsmokers are patients who have not consumed tobacco or nicotine-containing products for 1 year before the start of the study. Patients classified as current smokers must have smoked a minimum of 10 cigarettes per day for up to 1 year.

研究类型

介入性

注册 (实际的)

48

阶段

  • 阶段1

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

    • Florida
      • Fort Myers、Florida、美国、33916
        • Florida Cancer Specialists
    • Tennessee
      • Nashville、Tennessee、美国、37203
        • Tennessee Oncology

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

有资格学习的性别

全部

描述

  1. Histologically confirmed incurable solid tumors refractory to standard treatment or for which there is no known standard treatment.
  2. Two cohorts of patients will be enrolled: Cohort A will consist of patients who are current smokers, and Cohort B will consist of patients who are current nonsmokers. Nonsmokers are patients who have not consumed tobacco or nicotine-containing products for 1 year before the start of the study. Patients classified as current smokers must have smoked a minimum of 10 cigarettes per day for <1 year.
  3. Patients must have evaluable disease.
  4. Recovery from any toxic effects of prior therapy to grade 1 per the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0.
  5. Completion of radiation therapy at least 21 days prior to the start of study treatment (not including palliative local radiation).
  6. An Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  7. Absolute neutrophil count (ANC) >1,500/mL and platelets >75,000/mL (within 7 days prior to study treatment).
  8. Hemoglobin >9 g/dL (within 7 days prior to treatment). Patients may be transfused or receive erythropoietin to maintain or exceed this level where otherwise indicated.
  9. International normalized ratio (INR) <1.5 or prothrombin time (PT)/partial thromboplastin time (PTT) within normal limits (WNL) of the institution (if patient is not on anti-coagulation therapy; patients receiving anticoagulation treatment with an agent such as warfarin or heparin may be allowed to participate with the therapeutic range established prior to the initiation of study treatment).
  10. Serum creatinine <1.5 x the institutional upper limit of normal (ULN) within 7 days prior to study treatment. If the absolute value is greater than 2 mg/dL, the creatinine clearance (calculated according to the Cockcroft-Gault formula) must be > 45 mL/min for the patient to be eligible for the study.
  11. Transaminases <3 x the institutional ULN (except if there is known hepatic metastasis, wherein transaminases may be <5 x institutional ULN).
  12. Total bilirubin <1.5 times ULN.
  13. Patients must be able to understand the nature of this study, give written informed consent, and comply with study requirements.
  14. Agreement of female patients of childbearing potential and male patients who have partners of childbearing potential to use an effective form of contraception to prevent pregnancy during treatment, and for a minimum of 90 days thereafter. Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment.

Exclusion

  1. Patients with untreated brain metastases. Patients with neurological symptoms must undergo a CT scan/MRI of the brain to exclude brain metastasis. Patients who have a history of brain metastases that has been treated by surgery or radiation therapy > 4 weeks with no signs of Central Nervous System (CNS) progression are allowed.
  2. Women who are pregnant or lactating.
  3. Patients whose last dose of chemotherapy, immunotherapy, or investigational drug therapy was completed < 21 days prior to receiving study drug
  4. Significant cardiac disease within 90 days of starting study treatment including:

    • superior vena cava syndrome;
    • new onset angina;
    • congestive heart failure (CHF) > Class 2 per New York Heart Association (NYHA) classification (see Appendix B);
    • ventricular arrhythmia;
    • valvular heart disease.
  5. Myocardial infarction (MI) within 6 months prior to initiation of study treatment.
  6. Cardiomegaly on chest imaging or CHF > Class 2 per NYHA classification (see Appendix B) unless the left ventricular ejection fraction (LVEF) is within normal range for the institution within 3 months of initiating therapy.
  7. Poorly controlled hypertension (defined as systolic blood pressure [BP] >150 mmHg and/or diastolic blood pressure >90 mmHg on anti-hypertensive medications).
  8. Unstable angina (anginal symptoms at rest).
  9. Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
  10. Presence of cardiac disease that, in the opinion of the investigator, increases the risk of ventricular arrhythmia.
  11. A serious active infection (> grade 2) at the time of treatment
  12. A serious underlying medical condition that would impair the ability of the patient to receive protocol treatment.
  13. A major surgical procedure within 28 days of beginning treatment, or anticipation of the need for major surgery during the course of the study.
  14. Any minor surgery must be completed within 7 days prior to beginning study treatment.
  15. Use of rifampin, St. John's wort, or other potent inducers of CYP3A4 are not permitted from Day -14 through Day 15 of the study (see Appendix C).
  16. Use of ketoconazole and other potent inhibitors of CYP3A4 are not permitted from Day -14 through Day 15 of the study (see Appendix C).
  17. Stroke or transient ischemic attack (TIA) within the past 6 months.
  18. Any prior history of hypertensive crisis or hypertensive encephalopathy.
  19. Pulmonary hemorrhage/bleeding event > grade 2 within 28 days of study treatment.
  20. Any other non-pulmonary hemorrhage/bleeding event> grade 3 within 28 days of study treatment.
  21. Evidence or history of bleeding diathesis or coagulopathy.
  22. Serious non-healing wound, ulcer, or bone fracture.
  23. Known or suspected allergy/hypersensitivity to any agent given in the course of this trial.
  24. Patients with gastrointestinal (GI) tract disease, causing the inability to take oral medication, malabsorption syndrome, a requirement for intravenous (IV) alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease.
  25. Patients who smoke 1-9 cigarettes per day during the year before study entry or patients who have smoked for <1 year will not be eligible for this study.
  26. Any condition that impairs the patient's ability to swallow whole pills.
  27. Known human immunodeficiency virus (HIV) infection or chronic active Hepatitis B or C.

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: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:Erlotinib/Sorafenib
Patients will receive erlotinib 150 mg once daily by mouth and sorafenib 400 mg twice daily by mouth. The study will begin with a 2-week run-in period (which will begin on Day 14 of the study, and continue through Day 1 of the study), in which erlotinib will be dosed alone at 150 mg once daily. Patients will continue taking erlotinib as a single agent at 150 mg once daily through Day 1. After the 2-week run-in period, patients will receive continuous dosing of both agents (erlotinib 150 mg once daily and sorafenib 400 mg twice daily) in cycles of 28 days each. Toxicity will be assessed every cycle (every 4 weeks) for all patients. Because this is not an efficacy study, restaging tumor measurements will be at the discretion of the physician every 8 weeks during treatment. Patients with objective response or stable disease will continue therapy; patients with disease progression or unacceptable toxicity will be discontinued from the study.
150 mg once daily by mouth
其他名称:
  • 特罗凯
400 mg twice daily by mouth
其他名称:
  • 多吉美

研究衡量的是什么?

主要结果指标

结果测量
大体时间
To determine the pharmacokinetics (PK) of erlotinib when administered in combination with sorafenib on a continuous schedule in Refractory Solid Tumors in patients who are smokers and in patients who are nonsmokers.
大体时间:3 months
3 months

次要结果测量

结果测量
大体时间
To evaluate safety of this combination in patients with Refractory Solid Tumors.
大体时间:3 months
3 months

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。

合作者

调查人员

  • 学习椅:David R. Spigel, M.D.、SCRI Development Innovations, LLC

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

2008年10月1日

初级完成 (实际的)

2013年9月1日

研究完成 (实际的)

2014年6月1日

研究注册日期

首次提交

2008年9月24日

首先提交符合 QC 标准的

2008年9月24日

首次发布 (估计)

2008年9月25日

研究记录更新

最后更新发布 (估计)

2014年7月2日

上次提交的符合 QC 标准的更新

2014年7月1日

最后验证

2014年7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.

难治性实体瘤的临床试验

Erlotinib的临床试验

3
订阅