Phase II Trial of Pulsed Taxol With Concurrent Thoracic Radiotherapy, & Adjuvant Chemo in Stage III NSCLC
- Conditions
- Non Small Cell Lung Cancer
- Registration Number
- NCT00449657
- Lead Sponsor
- Leo W. Jenkins Cancer Center
- Brief Summary
This is a phase II study to evaluate the toxicity and overall survival of pulsed paclitaxel with concurrent thoracic radiotherapy, and adjuvant gemcitabine and carboplatin in stage IIIA and IIIB non-small cell lung cancer
- Detailed Description
OBJECTIVES Primary
1. Overall survival
2. Tumor response using RECIST criteria
Secondary
1. Determine the toxicity of the proposed treatment in this patient population.
2. Progression free survival
3. Locoregional control
4. Distant failure
STUDY DESIGN
Description of the Study Phase II study to evaluate the toxicity and overall survival of pulsed paclitaxel with concurrent thoracic radiotherapy, and adjuvant gemcitabine and carboplatin in stage IIIA and IIIB non-small cell lung cancer.
Rationale for Study Design The proposed doses of gemcitabine, carboplatin, paclitaxel, and thoracic radiation therapy have been previously studied and deemed safe. The design of this study is not to find the maximum tolerated dose (MTD) of these agents, but to study the toxicity and overall survival from this combination.
Outcome Measures Primary Outcome Measures
1. Overall survival
2. Tumor response using RECIST criteria
Secondary Outcome Measures
1. Locoregional control
2. Distant Failure
3. Progression free survival
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 24
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Patients must have: IIIA or IIIB non-small cell lung cancer by radiographic or surgical staging, excluding: superior sulcus tumors, tumors with associated atelectasis or obstructive pneumonitis of the entire lung, and tumors with a malignant pleural effusion.
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Patients will be included in the study based on the following criteria:
- Patients must be older than 18 years old.
- Patients must have a Zubrod performance status of 0 to 2
- Patients with adequate bone marrow function
- Patients with adequate renal function
- Patients with adequate hepatic function
- Patients of childbearing potential must have a negative serum pregnancy test and use an effective form of contraception.
- Patients who are suitable for treatment with radical intent using concurrent chemotherapy and radiation.
- Patients who have signed an approved informed consent and authorization permitting release of personal health information.
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Disease-Specific Exclusions
- Superior sulcus tumors
- Atelectasis or obstructive pneumonitis of the entire lung
- Malignant pleural effusion
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General Medical Exclusions
- Surgical candidates
- Patients who are pregnant at the time of diagnosis
- Serious concomitant systemic disorders incompatible with the study
- Inability to comply with study and/or follow-up procedures
- Life expectancy of less than 12 weeks
- Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an experimental drug study
- Patients with septicemia or severe infection.
- Patients who have circumstances that will not permit completion of this study or the required follow-up
- Patients with any contraindication to gemcitabine, carboplatin, or paclitaxel
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Tumor response using RECIST criteria 12/31/2014
- Secondary Outcome Measures
Name Time Method Locoregional control 12/31/2014 Distant failure 12/31/2014 Progression free survival 12/31/2014
Trial Locations
- Locations (1)
Brody School of Medicine at East Carolina University
🇺🇸Greenville, North Carolina, United States