Second Line Erlotinib (Tarceva) Plus Digoxin in Non-Small Cell Lung Cancer

Condition(s) targeted: Carcinoma, Non-Small Cell Lung

Intervention: Erlotinib plus Digoxin (Drug)

Phase: Phase 2

Status: Recruiting

Sponsored by: James Graham Brown Cancer Center

Official(s) and/or principal investigator(s):
Goetz H Kloecker, MD, MSPH, Principal Investigator, Affiliation: James Graham Brown Cancer Center/ University of Louisville

Overall contact:
Jamie M Day, BSN, Phone: (502) 562-3429, Email: jmluka01@louisville.edu

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.

Official title: Phase II Trial of Second Line Erlotinib + Digoxin in Patients With Non-Small Cell Lung Cancer

Study design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study

Primary outcome: Computed tomography (CT) Scans of chest & abdomen will be done to evaluate therapeutic response

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.

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

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)

Jamie M Day, BSN, Phone: (502) 562-3429, Email: jmluka01@louisville.edu

James Graham Brown Cancer Center, Louisville, Kentucky 40202, United States; Recruiting
Jamie M Day, BSN, Phone: 502-562-3429, Email: jmluka01@louisville.edu
Goetz H Kloecker, MD, MSPH, Principal Investigator
Donald M Miller, MD, PhD, Sub-Investigator
Damian Laber, MD, Sub-Investigator
Dharamvir Jain, MD, Sub-Investigator
Vivek Sharma, MD, Sub-Investigator
Fred Hendler, MD, PhD, Sub-Investigator

James Graham Brown Cancer Center

Starting date: February 2006
Ending date: February 2016
Last updated: September 10, 2008