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Chemotherapy Resistance and Sensitivity Testing in Lung Tumors

M

Marshall University

Status

Completed

Conditions

Lung Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT01570855
246601-1

Details and patient eligibility

About

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.

Full description

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.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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