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

2016년 3월 10일 업데이트: 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.

연구 개요

연구 유형

중재적

등록 (실제)

53

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
다른 이름들:
  • 넥사바
Erlotinib 150 mg once daily by mouth
다른 이름들:
  • 타세바
활성 비교기: 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.
다른 이름들:
  • 넥사바

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Progression-free Survival (PFS)
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Overall Response Rate
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 의자: David Spigel, M.D., SCRI Development Innovations, LLC

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2008년 3월 1일

기본 완료 (실제)

2012년 5월 1일

연구 완료 (실제)

2014년 11월 1일

연구 등록 날짜

최초 제출

2008년 1월 24일

QC 기준을 충족하는 최초 제출

2008년 1월 24일

처음 게시됨 (추정)

2008년 2월 7일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2016년 4월 8일

QC 기준을 충족하는 마지막 업데이트 제출

2016년 3월 10일

마지막으로 확인됨

2016년 3월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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