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Sorafenib and Erlotinib or Sorafenib Alone in Advanced Non-Small Cell Lung Cancer Progressing on Erlotinib

2016年3月10日 更新者:SCRI Development Innovations, LLC

Randomized Phase II Trial of Sorafenib and Erlotinib or Sorafenib Alone in Patients With Advanced Non-Small Cell Lung Cancer Progressing on Erlotinib

This is a randomized, open-label, multi-center, Phase II study of treatment of patients with advanced NSCLC who have progressed on erlotinib with the combination of sorafenib and erlotinib or sorafenib alone.

調査の概要

状態

完了

研究の種類

介入

入学 (実際)

53

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Florida
      • Fort Myers、Florida、アメリカ、33901
        • Florida Cancer Specialists
    • Georgia
      • Gainesville、Georgia、アメリカ、30501
        • Northeast Georgia Medical Center
      • Marietta、Georgia、アメリカ、30060
        • Wellstar Cancer Research
    • Indiana
      • Terre Haute、Indiana、アメリカ、47802
        • Providence Medical Group
    • Kentucky
      • Louisville、Kentucky、アメリカ、40207
        • Norton Cancer Institute
    • Louisiana
      • Baton Rouge、Louisiana、アメリカ、70806
        • Hematology Oncology Clinic, LLP
    • Maryland
      • Bethesda、Maryland、アメリカ、20817
        • Center for Cancer and Blood Disorders
      • Bethesda、Maryland、アメリカ、20817
        • National Capital Clinical Research Consortium
    • Mississippi
      • Jackson、Mississippi、アメリカ、39202
        • Jackson Oncology Associates
    • Missouri
      • Chesterfield、Missouri、アメリカ、63017
        • St. Louis Cancer Care
      • Kansas City、Missouri、アメリカ、64132
        • Research Medical Center
    • Nebraska
      • Omaha、Nebraska、アメリカ、68114
        • Nebraska Methodist Cancer Center
    • New Jersey
      • Morristown、New Jersey、アメリカ、07960
        • Hematology-Oncology Associates of Northern NJ
    • Tennessee
      • Chattanooga、Tennessee、アメリカ、37404
        • Chattanooga Oncology Hematology Associates
      • Chattanooga、Tennessee、アメリカ、37404
        • Associates in Hematology Oncology
      • Nashville、Tennessee、アメリカ、37023
        • Tennessee Oncology, PLLC

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  1. Histologically confirmed stage IIIB/IV or relapsed non-small cell lung carcinoma (squamous carcinoma, adenocarcinoma, or large cell carcinoma). Patients with mixed tumors with small-cell elements are ineligible.
  2. Patients with no more than 2 prior lines of therapy, with the latest of those therapies being single-agent erlotinib.
  3. Evidence of progressive disease on erlotinib as assessed by the treating physician. Erlotinib must be the last treatment for NSCLC prior to enrollment into this study. Patients may be on erlotinib until enrollment. If erlotinib has already been stopped, the period of time off Erlotinib cannot exceed 14 days prior to study enrollment.
  4. Patients must have experienced a clinical benefit (complete response [CR], partial response [PR], or stable disease [SD]) from prior therapy with erlotinib for a period of 8 weeks.
  5. Patient must have one measurable lesion measuring at least 10 mm in the longest diameter (LD) by spiral computed tomography (CT), or 20 mm with conventional techniques according to the Response Evaluation Criteria in Solid Tumors (RECIST).
  6. Recovery from any toxic effects of erlotinib to ≤ grade 1 per the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE).
  7. Completion of palliative radiation therapy prior to the start of study treatment. Previously irradiated lesions in the advanced setting cannot be included as target lesions unless clear tumor progression has been observed following the completion of radiation therapy.
  8. Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
  9. Absolute neutrophil count (ANC) >=1,500 and platelets >=75,000 (within 7 days prior to initial study treatment).
  10. Hemoglobin >=9 g/dL (within 7 days prior to initial treatment).
  11. International normalized ratio (INR) <=1.5 or prothrombin time (PT)/partial thromboplastin time (PTT) within normal limits (WNL) of the institution if not on anticoagulation therapy. Patients receiving anti-coagulation treatment with an agent such as warfarin or heparin may be allowed to participate with the therapeutic range established prior to study treatment initiation.
  12. Serum creatinine <=1.5 x institutional upper limit of normal (ULN) within 7 days prior to initial study treatment. If the absolute value is greater than 2mg/dL, the creatinine clearance, calculated according to the Cockroft-Gault formula, must be >=45 mL/min to be eligible.
  13. Bilirubin <=1.5 x the ULN; transaminases <=3 x institutional ULN, except in known hepatic metastasis, wherein these may be >=5 x institutional ULN.
  14. Patients must be able to understand the nature of this study, give written informed consent, and comply with study requirements.
  15. Agreement of male patients (with partners of childbearing potential) and female patients of childbearing potential to use effective contraception to prevent pregnancy during treatment and for a minimum of 90 days thereafter. Additionally, women should not breastfeed during this time.

Exclusion Criteria:

  1. Past or current history of neoplasm other than the entry diagnosis, with the exception of treated non-melanoma skin cancer or carcinoma in situ of the cervix, or other cancers cured by local therapy alone, and a disease-free survival (DFS) >=3 years.
  2. Pregnancy or lactation. All females of child-bearing potential must have negative serum or urine pregnancy tests within 7 days prior to study treatment.
  3. Prior epithelial growth factor receptor (EGFR) inhibitors, with the exception of erlotinib, are not allowed. This includes both tyrosine kinase inhibitors (TKIs) and monoclonal antibodies. Prior vascular endothelial growth factor (VEGF) inhibitors, with the exception of bevacizumab, are not allowed.
  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
    • arrhythmia
    • valvular heart disease.
  5. Myocardial infarction within 6 months prior to initiation of study treatment
  6. Cardiomegaly on chest imaging or ventricular hypertrophy on electrocardiogram (ECG) unless the left ventricular ejection fraction (LVEF) is within normal range for the institution.
  7. Poorly controlled hypertension (defined as systolic blood pressure [BP] >150 mm Hg and/or diastolic BP >100 mm Hg on antihypertensive 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. Untreated brain metastases. Patients who have treated metastases >=4 weeks out (with surgery and/or radiation therapy) and no evidence of central nervous system (CNS) progression are eligible.
  14. Treatment with a non-approved or investigational drug within 28 days of initial study treatment.
  15. A major surgical procedure, open biopsy, or significant traumatic injury within 28 days of beginning treatment or anticipation of need for major surgery during the course of the study.
  16. Thrombolic or embolic events such as a stroke and transient ischemic attack (TIA) within the past 6 months.
  17. Any prior history of hypertensive crisis or hypertensive encephalopathy.
  18. Pulmonary hemorrhage/bleeding event >= grade 2 within 28 days of initial study treatment.
  19. Any other non-pulmonary hemorrhage/bleeding event >= grade 3 within 28 days of initial study treatment.
  20. Evidence or history of bleeding diathesis or coagulopathy.
  21. Serious non-healing wound, ulcer, or bone fracture.
  22. Use of St. John's Wort or rifampin (rifampicin).
  23. Known or suspected allergy/hypersensitivity to any agent given in the course of this trial.
  24. Any malabsorption problem.
  25. Any condition that impairs the patient's ability to swallow whole pills.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Sorafenib+Erlotinib
Sorafenib 400 mg twice daily by mouth Erlotinib 150 mg once daily by mouth
Sorafenib 400 mg twice daily by mouth Study treatment will be given in cycles of 28 days. Patients will be re-staged every 2 treatment cycles (every 8 weeks). Patients with an objective response or stable disease will continue study treatment. Patients will continue until disease progression or intolerable toxicity occurs.
他の名前:
  • ネクサバール
Erlotinib 150 mg once daily by mouth
他の名前:
  • タルセバ
アクティブコンパレータ:Sorafenib
Sorafenib 400 mg twice daily by mouth.
Sorafenib 400 mg twice daily by mouth Study treatment will be given in cycles of 28 days. Patients will be re-staged every 2 treatment cycles (every 8 weeks). Patients with an objective response or stable disease will continue study treatment. Patients will continue until disease progression or intolerable toxicity occurs.
他の名前:
  • ネクサバール

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Progression-free Survival (PFS)
時間枠:18 months
The Length of Time, in Months, That Patients Were Alive From Their First Date of Protocol Treatment Until Worsening of Their Disease. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.
18 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall Response Rate
時間枠:18 months
The Number of Patients Who Experience an Objective Benefit From Treatment. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI or CT: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR.
18 months
Number of Participants With Treatment-emergent Adverse Events as a Measure of Safety and Tolerability
時間枠:18 months
Defined as the number of participants with treatment-emergent grade 3/4 adverse events utilizing the National Cancer Institute Common Technology Criteria for Adverse Events (NCI CTCAE) v3.0
18 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • スタディチェア:David Spigel, M.D.、SCRI Development Innovations, LLC

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2008年3月1日

一次修了 (実際)

2012年5月1日

研究の完了 (実際)

2014年11月1日

試験登録日

最初に提出

2008年1月24日

QC基準を満たした最初の提出物

2008年1月24日

最初の投稿 (見積もり)

2008年2月7日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年4月8日

QC基準を満たした最後の更新が送信されました

2016年3月10日

最終確認日

2016年3月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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