Expired Study
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Madison, Wisconsin 53792


Purpose:

- To determine if docetaxel and cisplatin can be administered in a dose intense manner in the adjuvant setting in resected non-small cell lung cancer - To evaluate the time to progression and overall survival - To evaluate toxicities of this chemotherapy combination in the adjuvant setting - To correlate XPD and ERCC1 polymorphisms with time to progression and toxicities in patients treated with this regimen


Criteria:

Inclusion Criteria: - Stage IB to IIIA non-small cell lung cancer completely resected within 4 to 8 weeks of initiating treatment on study - Performance Status ECOG 0 or 1 - Peripheral neuropathy: < grade 1 - Adequate blood cell counts - Adequate liver and hepatic function - Women of childbearing potential must have a negative pregnancy test. - Men and women of childbearing potential must be willing to consent to using effective contraception while on treatment and for at least 3 months thereafter Exclusion Criteria: - Patients with a history of severe hypersensitivity reaction to Docetaxel® or other drugs formulated with polysorbate 80. - Women who are breast-feeding. - Coexistent second malignancy or history of prior malignancy within previous 5 years (excluding basal or squamous cell carcinoma of the skin that has been treated curatively) - Uncontrolled cardiac disease or uncontrolled hypertension


NCT ID:

NCT00582634


Primary Contact:

Principal Investigator
Anne Traynor, MD
University of Wisconsin, Madison


Backup Contact:

N/A


Location Contact:

Madison, Wisconsin 53792
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

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