Erlotinib and Sorafenib in Chemonaive Patients With Locally Advanced or Metastatic Non Small Cell Lung Cancer
The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2009 by Free University Medical Center.
Recruitment status was Active, not recruiting
Information provided by:
Free University Medical Center
First received: July 24, 2008
Last updated: March 2, 2009
Last verified: March 2009
Patients with advanced or metastatic (stage IIIB-IV) non small cell lung cancer who have not received prior chemotherapy will be treated with erlotinib 150 mg once a day and sorafenib 400 mg twice a day. The objectives of the study are to assess the efficacy and safety of this combination treatment. Additional exploratory study objectives are correlation of biomarkers and imaging modalities potentially predictive for response and (progression free) survival.
Non-Small Cell Lung Cancer
Drug: sorafenib + erlotinib
||Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
||A Phase II Study of Erlotinib and Sorafenib in Patients With Locally Advanced and/or Metastatic (Stage IIIb or IV) Non Small Cell Lung Cancer Who Have Not Received Prior Chemotherapy
Primary Outcome Measures:
- Rate of non-progression at 6 weeks [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Best overall response rate [ Time Frame: end of study ] [ Designated as safety issue: No ]
- Duration of response [ Time Frame: End of study ] [ Designated as safety issue: No ]
- Survival [ Time Frame: End of study ] [ Designated as safety issue: No ]
- Toxicity [ Time Frame: Week 1, week 3, week 6, week 9, week 12 then every 6 weeks ] [ Designated as safety issue: Yes ]
- Prediction of early response and effects on tumor vascularisation by PET and perfusion CT scans [ Time Frame: Baseline, week 3 and week 6 ] [ Designated as safety issue: No ]
- Biomarkers for response (Proteomics, circulating cells, mutational analysis) [ Time Frame: Baseline, week 1, week 3 and week 6 ] [ Designated as safety issue: No ]
| Estimated Enrollment:
| Study Start Date:
| Estimated Study Completion Date:
| Estimated Primary Completion Date:
||November 2008 (Final data collection date for primary outcome measure)
Drug: sorafenib + erlotinib
sorafenib 400mg b.i.d oral Erlotinib 150 mg o.i.d oral
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Histologically/cytologically advanced NSCLC stage IIIB or IV
- No prior chemotherapy or therapy with systemic anti-tumor therapy (e.g., monoclonal antibody therapy) or prior exposure to agents directed at the HER axis (e.g. EGFR TK inhibitors, Herceptin). Prior surgery and/or localized irradiation is permitted provided that the irradiated lesion is not the only measurable lesion.
- Age > 18 years.
- ECOG Performance Status of 0 or 1
- Life expectancy of at least 12 weeks.
- Subjects with at least one uni-dimensional(for RECIST) measurable lesion. Lesions must be measured by CT-scan.
- Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to screening:
- Hemoglobin > 9.0 g/dl
- Absolute neutrophil count (ANC) >1,500/mm3
- Platelet count > 100,000/μl
- Total bilirubin < 1.5 times the upper limit of normal
- ALT and AST < 2.5 x upper limit of normal (< 5 x upper limit of normal for patients with liver involvement of their cancer)
- Alkaline phosphatase < 4 x ULN
- PT-INR/PTT < 1.5 x upper limit of normal [Patients who are being therapeutically anticoagulated with low molecular weight heparin will be allowed to participate provided that no prior evidence of underlying abnormality in these parameters exists.]
- Serum creatinine < 1.5 x upper limit of normal.
- Written informed consent.
Excluded medical conditions:
- History of cardiac disease: congestive heart failure >NYHA class 2; active CAD (MI more than 6 mo prior to study entry is allowed); cardiac arrhythmias requiring anti-arrhythmic therapy( beta blockers or digoxin are permitted) or uncontrolled hypertension.
- History of HIV infection or chronic hepatitis B or C.
- Active clinically serious infections (> grade 2 NCI-CTC version 3.0)
- Symptomatic metastatic brain or meningeal tumors (unless the patient is > 1 months from definitive radiotherapy and off steroids):
- Patients with seizure disorder requiring medication (such as steroids or anti-epileptics)
- History of organ allograft.
- Patients with evidence or history of bleeding diathesis
- Patients undergoing renal dialysis
- Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors [Ta, Tis & T1] or any cancer curatively treated > 3 years prior to study entry.
Excluded therapies and medications, previous and concomitant:
- Anticancer chemotherapy or immunotherapy during the study or within 4 weeks of study entry.
- Radiotherapy during study or within 3 weeks of start of study drug. (Palliative radiotherapy will be allowed). Major surgery within 3 weeks of start of study
- Autologous bone marrow transplant or stem cell rescue within 4 months of study
- Use of biologic response modifiers, such as G-CSF, within 3 week of study entry. [G-CSF and other hematopoietic growth factors may be used in the management of acute toxicity such as febrile neutropenia when clinically indicated or at the discretion of the investigator, however they may not be substituted for a required dose reduction.] [Patients taking chronic erythropoietin are permitted provided no dose adjustment is undertaken within 2 months prior to the study or during the study]
- Investigational drug therapy outside of this trial during or within 4 weeks of study entry
- Prior exposure to the study drugs.
- Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test performed within 7 days of the start of treatment. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and two weeks after the completion of trial.
- Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
- Any condition that is unstable or could jeopardize the safety of the patient and their compliance in the study
- Patients unable to swallow oral medications.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00722969
|VU university medical center
|Amsterdam, Netherlands, 1007 MB |
|Netherlands Cancer Institute
|Amsterdam, Netherlands |
|University Medical Center Groningen
|Groningen, Netherlands |
|University Hospital Maastricht
|Maastricht, Netherlands |
Free University Medical Center
||Egbert F Smit, Phd, MD
||VU University Medical Center
No publications provided
||Prof Dr E.F. smit, VU University Medical Center
History of Changes
|Other Study ID Numbers:
||07/203, EudraCT: 2007-004625-14
|Study First Received:
||July 24, 2008
||March 2, 2009
||Netherlands: Medical Ethics Review Committee (METC)
Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Keywords provided by Free University Medical Center:
non-small cell lung cancer
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on May 22, 2013
Carcinoma, Non-Small-Cell Lung
Respiratory Tract Neoplasms
Neoplasms by Site
Respiratory Tract Diseases
Protein Kinase Inhibitors
Molecular Mechanisms of Pharmacological Action