TARCEVA (Erlotinib) in Combination With Chemoradiation in Patients With Stage IIIA/B Non-Small Cell Lung Cancer (NSCLC)
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT00563784
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Erlotinib — DRUG150 mg by mouth daily for 7 Weeks
- Carboplatin — DRUG2 AUC by vein weekly for 7 Weeks
- Paclitaxel — DRUG45 mg/m\^2 by vein weekly for 7 Weeks
- Radiation Therapy — RADIATION63 GY/35 fractions for 7 weeks (+/- 5 days)
Study Details
The goal of this clinical research study is to find out if erlotinib given with chemotherapy and radiation therapy can help to control NSCLC. The safety of this combination treatment will also be studied. Researchers will also test the tissue from your earlier biopsy to measure the levels of epidermal growth factor receptor (EGFR). The purpose of EGFR testing is to learn about any link between various forms of EGFR and your response to treatment with erlotinib.
Key Dates
- First listed
- Nov 26, 2007
- Start date
- Nov 30, 2007
- Status verified
- Nov 2019
- Primary completion
- May 30, 2018
- Completion
- May 30, 2018
Study Design
- Enrollment
- 68 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Erlotinib + Paclitaxel + CarboplatinOral Erlotinib 150 mg daily + Paclitaxel 45 mg/m\^2 by vein weekly + Carboplatin 2 AUC by vein weekly and Radiation Therapy 63 GY/35 fractions for 7 weeks cycles
Primary Outcome Measure
Time To First Disease Progression [ Time Frame: From date of registration until the date of first documented progression or death from any cause, or lost to follow up, whichever came first, assessed up to 5 years. ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Texas MD Anderson Cancer Center | Houston | Texas | 77030 | - |
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