Chemotherapy Resistance and Sensitivity Testing in Lung Tumors
Status: | Completed |
---|---|
Conditions: | Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 5/3/2014 |
Start Date: | October 2011 |
End Date: | June 2014 |
Contact: | Pier P. Claudio, M.D., Ph.D. |
Email: | claudiop@marshall.edu |
Phone: | 304-696-3516 |
The purpose of this study is to screen chemotherapy drugs currently used to treat lung
cancer and determine the most effective treatment based on results of chemo sensitivity
testing on the patients own cancer cells in the laboratory. The results of this screening
will not influence the patients treatment.
cancer and determine the most effective treatment based on results of chemo sensitivity
testing on the patients own cancer cells in the laboratory. The results of this screening
will not influence the patients treatment.
The chemosensitivity assay will be performed on tissue obtained during the diagnostic fine
needle aspiration, core biopsy, or excisional biopsy of the lung lesion. Cancer cells (Bulk
of tumor) and Cancer Stem Cells (CSCs) will be isolated and expanded in the laboratory.
The drug screening assay will be used to evaluate the response of the CSCs and of the cancer
cells to the various chemotherapy regimens.
needle aspiration, core biopsy, or excisional biopsy of the lung lesion. Cancer cells (Bulk
of tumor) and Cancer Stem Cells (CSCs) will be isolated and expanded in the laboratory.
The drug screening assay will be used to evaluate the response of the CSCs and of the cancer
cells to the various chemotherapy regimens.
Inclusion Criteria:
- suspected or confirmed diagnosis of lung cancer
- undergoing a fine needle aspiration, core biopsy, or excisional biopsy for
diagnosis.
- Chemotherapy must be clinically indicated for treatment of the patient's qualifying
disease
- Patient must be at least 18 years of age
- Patient must have signed an IRB approved informed consent form for the data
collection study prior to entry of data into the enrollment form in the database.
Exclusion Criteria:
- Patient pathology shows benign pathology for sample submitted
- Patient is not indicated to receive chemotherapy for their disease
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