Carcinoma, Non-Small Cell Lung
Conditions
Keywords
non-small cell lung cancer, Erlotinib, Digoxin
Brief summary
The purpose of this study is to determine the potential benefit of adding Digoxin to erlotinib (Tarceva) treatment for patients with non-small cell lung cancer.
Detailed description
Non-small cell lung cancer (NSCLC) accounts for 80% of all lung cancer cases. The majority of NSCLC patients have advanced disease at the time of diagnosis, which usually requires treatment beyond standard first-line chemotherapy. Until recently, patients were limited in the number of options available for second-line treatment of NSCLC. In 2004, erlotinib was approved by the FDA for second and third-line treatment of NSCLC. Erlotinib is a cancer chemotherapy medication that slows the growth and spread of cancer cells in the body. Recent research suggests that a medication called Digoxin can sensitize cancer cells to respond better to chemotherapy. Digoxin is normally used to treat certain heart conditions by helping the heart beat more strongly and regularly and is not approved by the FDA for the treatment of NSCLC. Investigators hope that subject response rates to standard erlotinib therapy will be significantly improved by the addition of Digoxin. The purpose of this study is to determine the tumor response rate and overall survival of patients with non-small cell lung cancer treated with a daily regimen of erlotinib (Tarceva) plus Digoxin.
Interventions
DRUGErlotinib plus Digoxin
Each subject will receive erlotinib and digoxin daily until progression.
Sponsors
James Graham Brown Cancer Center
University of Louisville
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* diagnosis of non-small cell lung cancer * measurable or evaluable disease * primary tumor must be documented by histopathic analysis * disease recurrences occurring greater than five years after original diagnosis must be biopsy proven * treatment with only one prior chemotherapy regimen for advanced disease (one additional prior regimen was allowed for neoadjuvant, adjuvant, or neoadjuvant plus adjuvant therapy) * serum creatinine \< 2mg/dl, or a calculated creatinine clearance \> 40cc/min using the following formula: (140-age) x WT(kg) x 0.85 (if female 0.72) x creatinine (mg/dl). Tests must be done within 28 days prior to registration * must have a CT scan (chest & abdomen) within 4 weeks prior to registration * Zubrod performance status of 0-3
Exclusion criteria
* women who are pregnant or nursing * no other prior malignancy is allowed except for: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated Stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease-free for 5 years * history of ventricular fibrillation, sinus node or AV nodal disease, Wolff Parkinson White Syndrome, evidence of congestive heart failure, chest pain with exertion, hemodynamically significant or life threatening cardiac arrhythmia, or evidence of prior myocardial infarction on EKG. EKG must have been done within 28 days prior to registration. A normal cardiac stress test within 182 days prior to registration is required for all patients over 50 years old or those with abnormal EKG or any history of cardiac disease. * hypersensitivity to erlotinib and/or Digoxin * abnormal levels of K, Mg, and/or Ca, or conditions which cause such abnormalities (e.g. malnutrition, severe diarrhea, prolonged vomiting, dialysis, GI suction, untreated hypothyroidism, and use of diuretics, amphotericin B, steroids, or antacids)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Therapeutic Response, Evaluated by Computed Tomography (CT) Scans of Chest & Abdomen. | Measured every 6 weeks after baseline until disease progression, an average of 3 months |
Participant flow
Recruitment details
Patient accrual lasted from March 2006 until August 2008 and was stopped early at the time of interim analysis. 24 who completed at least 6 weeks of therapy are presented here.
Participants by arm
| Arm | Count |
|---|---|
| Erlotinib and Digoxin Erlotinib plus Digoxin
Erlotinib plus Digoxin : Each subject will receive erlotinib and digoxin daily until progression. | 26 |
| Total | 26 |
Baseline characteristics
| Characteristic | Erlotinib and Digoxin |
|---|---|
| Age, Continuous | 61 years |
| Age, Customized <=18 years | 0 participants |
| Age, Customized >18 years | 26 participants |
| Sex: Female, Male Female | 16 Participants |
| Sex: Female, Male Male | 10 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 20 / 24 |
| serious Total, serious adverse events | 0 / 24 |
Outcome results
Primary
Therapeutic Response, Evaluated by Computed Tomography (CT) Scans of Chest & Abdomen.
Time frame: Measured every 6 weeks after baseline until disease progression, an average of 3 months
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Erlotinib and Digoxin | Therapeutic Response, Evaluated by Computed Tomography (CT) Scans of Chest & Abdomen. | Partial Response | 1 participants |
| Erlotinib and Digoxin | Therapeutic Response, Evaluated by Computed Tomography (CT) Scans of Chest & Abdomen. | Stable Disease | 9 participants |
| Erlotinib and Digoxin | Therapeutic Response, Evaluated by Computed Tomography (CT) Scans of Chest & Abdomen. | Progressive Disease | 14 participants |