Status:
COMPLETED
Pemetrexed Disodium, Carboplatin, and Radiation Therapy With or Without Cetuximab in Treating Patients With Stage III Non-Small Cell Lung Cancer
Lead Sponsor:
Alliance for Clinical Trials in Oncology
Collaborating Sponsors:
National Cancer Institute (NCI)
Eli Lilly and Company
Conditions:
Lung Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
RATIONALE: Pemetrexed disodium may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as carboplatin, work in different ways to sto...
Detailed Description
OBJECTIVES: Primary * Determine the overall survival of patients with unresectable stage III non-small cell lung cancer treated with pemetrexed disodium, carboplatin, and thoracic radiotherapy with ...
Eligibility Criteria
Inclusion
- Histologically or cytologically documented NSCLC, including squamous cell carcinoma, adenocarcinoma including bronchoalveolar cell, and large cell anaplastic carcinoma (including giant and clear cell carcinomas)
- Eligible Disease Stages: Inoperable IIIA and Selected IIIB - Patients entered must be considered unresectable or inoperable. Patients do not need to have a mediastinoscopy.
- A size of 2 cm or greater by CT is a sufficient criterion for the diagnosis of mediastinal lymph node (N2 or N3) involvement by malignancy. If the largest mediastinal lymph node is less than 2 cm in diameter, a biopsy confirmation of mediastinal nodal involvement is required.
- The following patients are eligible:
- Patients must be M0
- Patients with any T with N2 or N3 are eligible
- Patients with T3, N1-N3 disease are eligible if deemed unresectable
- Patients with T4, any N are eligible provided the T4 status is not determined because of malignant effusion
- Patients with contralateral mediastinal disease (N3) are eligible if all gross disease can be encompassed in the radiation field in accordance with the homogeneity criteria
- Patients with a pleural effusion, which is a transudate, cytologically negative and non-bloody, are eligible if the radiation oncologist feels the tumor can be encompassed within a reasonable field of radiotherapy
- If a pleural effusion can be seen on the chest CT but not on CXR and is too small to tap, the patient will be eligible. Patients who develop a new pleural effusion after thoracotomy or other invasive thoracic procedure will be eligible.
- The following patients are NOT eligible:
- Patients with T3, N0 disease
- Patients with M1 disease
- Patients with atelectasis of the entire lung
- Patients with direct invasion of vertebral body
- Patients with scalene, supraclavicular, or contralateral hilar node involvement
- Patients with exudative, bloody, or cytologically malignant effusions
- Patients must have Measurable Disease: Lesions that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 20 mm with conventional techniques or as ≥10 mm with spiral CT scan. Lesions that are not considered measurable include bone lesions, leptomeningeal disease, ascites, pleural/pericardial effusion, abdominal masses that are not confirmed and followed by imaging techniques, cystic lesions and tumor lesions situated in a previously irradiated area.
- Prior Therapy: ≥ 2 weeks since formal exploratory thoracotomy. No prior chemotherapy for NSCLC, chest radiation therapy or therapy that specifically and directly targets the EGFR pathway
- ECOG performance status 0-1
- Positron Emission Tomography (PET) using 18 fluorodeoxyglucose (FDG) must be negative for distant metastasis. PET imaging is mandatory.
- Weight loss of ≤ 10% in the past 3 months
- No "currently active" second malignancy other than non-melanoma skin cancers. Patients are not considered to have a "currently active" malignancy if they have completed therapy and are considered by their physician to be at less than 30% risk of relapse.
- Non-pregnant and non-nursing because of significant risk to the fetus/infant
- Age ≥ 18 years
- No patients with uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness.
- No HIV-positive patients receiving combination anti-retroviral therapy because patients with immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy
- No known history of hypersensitivity to carboplatin, pemetrexed or a monoclonal antibody
- Required Initial Laboratory Values:
- Granulocytes ≥ 1,500/mcl
- Platelets ≥ 100,000/mcl
- Calculated Creatinine Clearance ≥ 45 ml/min
- Bilirubin \< 1.5 x ULN
- AST/ALT \< 3 x ULN
- Alkaline Phosphatase \< 3 x ULN
Exclusion
Key Trial Info
Start Date :
September 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2012
Estimated Enrollment :
109 Patients enrolled
Trial Details
Trial ID
NCT00117962
Start Date
September 1 2005
End Date
September 1 2012
Last Update
October 7 2016
Active Locations (71)
Enter a location and click search to find clinical trials sorted by distance.
1
Arroyo Grande Community Hospital
Arroyo Grande, California, United States, 93420
2
Eden Medical Center
Castro Valley, California, United States, 94546
3
Saint Rose Hospital
Hayward, California, United States, 94545
4
Rebecca and John Moores UCSD Cancer Center
La Jolla, California, United States, 92093-0658