Sorafenib and Erlotinib or Sorafenib Alone in Advanced Non-Small Cell Lung Cancer Progressing on Erlotinib
Randomized Phase II Trial of Sorafenib and Erlotinib or Sorafenib Alone in Patients With Advanced Non-Small Cell Lung Cancer Progressing on Erlotinib
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 2
Contacts and Locations
Study Locations
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-
Florida
-
Fort Myers, Florida, United States, 33901
- Florida Cancer Specialists
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Georgia
-
Gainesville, Georgia, United States, 30501
- Northeast Georgia Medical Center
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Marietta, Georgia, United States, 30060
- Wellstar Cancer Research
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Indiana
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Terre Haute, Indiana, United States, 47802
- Providence Medical Group
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Kentucky
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Louisville, Kentucky, United States, 40207
- Norton Cancer Institute
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Louisiana
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Baton Rouge, Louisiana, United States, 70806
- Hematology Oncology Clinic, LLP
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Maryland
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Bethesda, Maryland, United States, 20817
- Center for Cancer and Blood Disorders
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Bethesda, Maryland, United States, 20817
- National Capital Clinical Research Consortium
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Mississippi
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Jackson, Mississippi, United States, 39202
- Jackson Oncology Associates
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Missouri
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Chesterfield, Missouri, United States, 63017
- St. Louis Cancer Care
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Kansas City, Missouri, United States, 64132
- Research Medical Center
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Nebraska
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Omaha, Nebraska, United States, 68114
- Nebraska Methodist Cancer Center
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New Jersey
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Morristown, New Jersey, United States, 07960
- Hematology-Oncology Associates of Northern NJ
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Tennessee
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Chattanooga, Tennessee, United States, 37404
- Chattanooga Oncology Hematology Associates
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Chattanooga, Tennessee, United States, 37404
- Associates in Hematology Oncology
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Nashville, Tennessee, United States, 37023
- Tennessee Oncology, PLLC
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-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 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.
- Patients with no more than 2 prior lines of therapy, with the latest of those therapies being single-agent erlotinib.
- 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.
- 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.
- 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).
- Recovery from any toxic effects of erlotinib to ≤ grade 1 per the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE).
- 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.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
- Absolute neutrophil count (ANC) >=1,500 and platelets >=75,000 (within 7 days prior to initial study treatment).
- Hemoglobin >=9 g/dL (within 7 days prior to initial treatment).
- 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.
- 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.
- Bilirubin <=1.5 x the ULN; transaminases <=3 x institutional ULN, except in known hepatic metastasis, wherein these may be >=5 x institutional ULN.
- Patients must be able to understand the nature of this study, give written informed consent, and comply with study requirements.
- 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:
- 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.
- Pregnancy or lactation. All females of child-bearing potential must have negative serum or urine pregnancy tests within 7 days prior to study treatment.
- 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.
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.
- Myocardial infarction within 6 months prior to initiation of study treatment
- Cardiomegaly on chest imaging or ventricular hypertrophy on electrocardiogram (ECG) unless the left ventricular ejection fraction (LVEF) is within normal range for the institution.
- Poorly controlled hypertension (defined as systolic blood pressure [BP] >150 mm Hg and/or diastolic BP >100 mm Hg on antihypertensive medications).
- Unstable angina (anginal symptoms at rest).
- Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
- Presence of cardiac disease that, in the opinion of the investigator, increases the risk of ventricular arrhythmia.
- A serious active infection (> grade 2) at the time of treatment
- A serious underlying medical condition that would impair the ability of the patient to receive protocol treatment.
- 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.
- Treatment with a non-approved or investigational drug within 28 days of initial study treatment.
- 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.
- Thrombolic or embolic events such as a stroke and transient ischemic attack (TIA) within the past 6 months.
- Any prior history of hypertensive crisis or hypertensive encephalopathy.
- Pulmonary hemorrhage/bleeding event >= grade 2 within 28 days of initial study treatment.
- Any other non-pulmonary hemorrhage/bleeding event >= grade 3 within 28 days of initial study treatment.
- Evidence or history of bleeding diathesis or coagulopathy.
- Serious non-healing wound, ulcer, or bone fracture.
- Use of St. John's Wort or rifampin (rifampicin).
- Known or suspected allergy/hypersensitivity to any agent given in the course of this trial.
- Any malabsorption problem.
- Any condition that impairs the patient's ability to swallow whole pills.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Sorafenib+Erlotinib
Sorafenib 400 mg twice daily by mouth Erlotinib 150 mg once daily by mouth
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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.
Other Names:
Erlotinib 150 mg once daily by mouth
Other Names:
|
|
Active Comparator: 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.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Progression-free Survival (PFS)
Time Frame: 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
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Overall Response Rate
Time Frame: 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.
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18 months
|
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Number of Participants With Treatment-emergent Adverse Events as a Measure of Safety and Tolerability
Time Frame: 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
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Study Chair: David Spigel, M.D., SCRI Development Innovations, LLC
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Respiratory Tract Diseases
- Neoplasms
- Lung Diseases
- Neoplasms by Site
- Respiratory Tract Neoplasms
- Thoracic Neoplasms
- Carcinoma, Bronchogenic
- Bronchial Neoplasms
- Lung Neoplasms
- Carcinoma, Non-Small-Cell Lung
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Antineoplastic Agents
- Protein Kinase Inhibitors
- Erlotinib Hydrochloride
- Sorafenib
Other Study ID Numbers
Other Study ID Numbers
- SCRI LUN 162
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