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Sponsors and Collaborators: |
Clinical Oncology Research Associates Aventis Pharmaceuticals |
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Information provided by: | Clinical Oncology Research Associates |
ClinicalTrials.gov Identifier: | NCT00256789 |
This program is designed for the treatment of patients with advanced non-small cell lung cancer. The study is designed for patients whose cancer is too advanced and therefore cannot be operated with the goal of completely removing the cancer. Patients at this stage of their disease traditionally receive radiation therapy or chemotherapy or both treatments in succession. Recently, the administration of both methods of treatment has been employed and preliminary studies indicate somewhat better results. Specifically, a new class of chemotherapy agents called taxanes used in combination with radiation therapy appear promising as determined in small studies.
However, the best treatment for this type of cancer has not been established yet. One goal of this study is to investigate if the combination of the new drug Taxotere (a drug belonging to the taxane class) given on the day of the radiation is well tolerated and will result in enhanced shrinkage of the cancer compared to traditional radiation therapy. In this study the radiation will be given on one day, rather than divided over five days per week (Monday through Friday) as in previous studies. Previous research has shown that both equal in how effective they are in treating lung cancer. The study will use the drug Taxotere in conjunction with radiation therapy.
Taxotere is an approved medicine by the United States Food and Drug Administration for the treatment of lung cancer. The purpose of this study is to evaluate if the chemotherapy drug Taxotere administered once weekly together with concurrent radiation on the same day is effective in shrinking non-small cell lung cancer. This trial will also investigate how well this treatment is tolerated and what effects this treatment will have on the everyday life and activities of participants.
Condition | Intervention |
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Carcinoma, Non-Small-Cell Lung |
Procedure: Radiation Drug: Chemotherapy |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Official Title: | Combination of Weekly Radiation and Docetaxel for Locally Advanced Non Small Cell Lung Cancer: A Feasibility Study |
Estimated Enrollment: | 40 |
Study Start Date: | September 2002 |
Estimated Study Completion Date: | November 2007 |
40 patients with locally advanced and metastatic NSCLC will be enrolled (stages III and IV) and treated once per week for a total of 12 cycles (12 weeks) according to the schedule outlined below.
Chemotherapy: The suggested phase II dose for weekly Taxotere with concomitant standard chest radiotherapy was determined to be 20mg/m2. In our unpublished phase I clinical trial, we found 35 mg/m2 to be well tolerated and therefore this dose is chosen for this phase II study. The drug will be administered intravenously on the same day as the radiation. All patients will be premedicated 12 hours prior to chemotherapy with Decadrone. Patients will be followed and evaluated weekly by a physician.
Radiation therapy: Although radiation was delivered differently in previous Taxotere based combined modality studies, the total radiation dose remains the same. Treatment will be given to a large field with a 2-3 cm tumor margin. All involved or suspicious nodal areas will be radiated as well. To reduce volume toxicity, the “field within a field” technique will be employed. Tumor and involved nodes will receive 200 cGy + 300 cGy. A total of 12 treatments will be administered in weekly, single sessions. Total treatment will be 6000 cGy. Radiation treatment will be administered 24 hours after Taxotere infusion.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients must be at least 18 years old.
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Exclusion Criteria:
Not falling into the eligibility criteria outlined above
Contact: Judy Motlow | 251 5435 4458 | JOM56@aol.com |
Contact: Paul Schwarzenberger, MD | 251 544 1009 | POSCHWARZ@YAHOO.COM |
United States, Alabama | |
Cancer Center and Mobile Infirmary Hospital | Recruiting |
Mobile, Alabama, United States, 36607 | |
Principal Investigator: Paul Schwarzenberger, MD | |
Sub-Investigator: Robert Gilbert, MD | |
Sub-Investigator: Frank Pitruzzello, MD | |
Sub-Investigator: Nicole Angel, MD |
Principal Investigator: | Paul Schwarzenberger, MD | Mobile Infirmary Hospital, Mobile, AL |
Study ID Numbers: | Hypo 1 |
Study First Received: | November 18, 2005 |
Last Updated: | November 18, 2005 |
ClinicalTrials.gov Identifier: | NCT00256789 History of Changes |
Health Authority: | United States: Institutional Review Board |
NSCLC, Non-Small Cell Lung Cancer,Weekly Radiation, Taxotere |
Docetaxel Thoracic Neoplasms Respiratory Tract Diseases Lung Neoplasms Lung Diseases |
Non-small Cell Lung Cancer Carcinoma, Non-Small-Cell Lung Neoplasms, Glandular and Epithelial Carcinoma |
Thoracic Neoplasms Respiratory Tract Neoplasms Neoplasms Neoplasms by Site Neoplasms by Histologic Type Respiratory Tract Diseases |
Lung Neoplasms Lung Diseases Carcinoma, Non-Small-Cell Lung Neoplasms, Glandular and Epithelial Carcinoma |