Lung Cancer Clinical Trial

First-Line Treatment of A Comparison of 2 Treatments in Elderly Patients With Advanced NSCLC

Summary

This trial will look at 2 different drug combinations that have well known safety profiles and are known to be active against non small cell lung cancer and combine them with bevacizumab, an experimental drug that has shown effectiveness when added to other drug combinations for advanced non-small cell lung cancer. The primary objective in this study is to see how well this combination of drugs keeps the cancer from getting worse in this elderly population of non-small cell lung cancer patients.

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Full Description

Patients in this study will be assigned to one of 2 treatment groups. The selection of the treatment groups will be done randomly by a computer.

The first group, Cohort A, will receive bevacizumab 10mg/kg by vein over 30-90 minutes followed by pemetrexed 500 mg/m2 by vein over 10 minutes followed by gemcitabine 1500 mg/m2 by vein over 30-60 minutes. This regimen will be given on day 1 and day 15 of each treatment cycle. Each cycle is 28 days long. As long as their disease does not worsen patients can receive up to a maximum of 6 cycles of this combination chemotherapy. Following that they can receive bevacizumab alone once every 2 weeks as long as their disease does not worsen.

The second group, Cohort B, will receive bevacizumab 15mg/kg by vein over 30-90 minutes followed by pemetrexed 500 mg/m2 by vein over approximately 10 minutes followed by carboplatin AUC=5 by vein over 30-60 minutes. This regimen will be given on day 1 of each treatment cycle. Each cycle is 21 days long. As long as their disease does not worsen patients can receive up to a maximum of 6 cycles of this combination chemotherapy. Following that they can receive bevacizumab alone once every 3 weeks as long as their disease does not worsen.

In both regimens vitamin B12 injections and Folic Acid pills will be given to reduce the occurrence of side effects from the treatment.

Each patient's disease will be evaluated at intervals by the proper scans or X-rays to see how well the cancer is responding to the treatment.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically confirmed non-small cell bronchogenic carcinoma, (adenocarcinoma, or large cell carcinoma)
Patients who have newly diagnosed unresectable stage III or stage IV disease are eligible.
Must be at least 70 years of age
Must have measurable disease by CT scan
Must be able to be up and about and care for themselves
May not have received prior treatment for stage III or IV disease
Must have adequate white and red blood cells and platelets.
Must be able to take Vitamin B12, Folic Acid and dexamethasone as stated in the study
Must be able to understand the nature of this study and give written informed consent
Adequate liver and kidney function

Exclusion Criteria:

Past or current history of cancer 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 have been disease free for five years
Female patients who are pregnant or are lactating are ineligible
History of unstable angina or myocardial infarction within 6 months prior to beginning bevacizumab
Brain metastasis - cancer that has spread to the brain
Major surgical procedure, open biopsy, or significant traumatic injury within 6 weeks of beginning bevacizumab or anticipation of need for major surgical procedure during the course of the study
Full-dose oral or by vein anticoagulation or receiving anti-clotting therapy within 10 days of starting treatment
Serious nonhealing wound, ulcer, or bone fracture
Bleeding or clotting disorders
Uncontrolled high blood pressure or serious heart arrhythmia requiring medication
History of abdominal fistula, gastrointestinal perforation, or intra- abdominal abscess within 6 months prior to beginning bevacizumab
Chronic non-steroidal anti-inflammatory use is not allowed on study
History of stroke or TIAs within the last 6 months

Please Note: There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have.

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

110

Study ID:

NCT00456261

Recruitment Status:

Completed

Sponsor:

SCRI Development Innovations, LLC

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There are 17 Locations for this study

See Locations Near You

Northeast Alabama Regional Medical Center
Anniston Alabama, 36207, United States
NEA Baptist Clinic
Jonesboro Arkansas, 72401, United States
Florida Cancer Specialists
Fort Myers Florida, 33901, United States
Watson Clinic Center for Cancer Care and Research
Lakeland Florida, 33805, United States
Northeast Georgia Medical Center
Gainesville Georgia, 30501, United States
Wellstar Cancer Research
Marietta Georgia, 30060, United States
Providence Medical Group
Terre Haute Indiana, 47802, United States
Graves-Gilbert Clinic
Bowling Green Kentucky, 42101, United States
Consultants in Blood Disorders and Cancer
Louisville Kentucky, 40207, United States
Mercy Hospital
Portland Maine, 04101, United States
Grand Rapids Clinical Oncology Program
Grand Rapids Michigan, 49503, United States
Methodist Cancer Center
Omaha Nebraska, 68114, United States
Cancer Care of Western North Carolina
Asheville North Carolina, 28801, United States
Oncology Hematology Care
Cincinnati Ohio, 45242, United States
Spartanburg Regional Medical Center
Spartanburg South Carolina, 29303, United States
Associates in Hematology Oncology
Chattanooga Tennessee, 37404, United States
Chattanooga Oncology Hematology Associates
Chattanooga Tennessee, 37404, United States
Tennessee Oncology, PLLC
Nashville Tennessee, 37023, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

110

Study ID:

NCT00456261

Recruitment Status:

Completed

Sponsor:


SCRI Development Innovations, LLC

How clear is this clinincal trial information?

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