Study of Tissue Samples From Patients With Stage I Non-Small Cell Lung Cancer Enrolled on Research Study CALGB-140202

Inclusion criteria

1. Registration to CALGB 140202 2. Institutional Review Board (IRB) review and approval at the institutions where the laboratory work will be performed is required 3. Informed Consent: The CALGB does not require that a separate consent form be signed for this study * The subject population to be studied in this protocol includes patients selected from CALGB 140202. All such patients have signed a written informed consent document meeting all federal, state and institutional guidelines as part of entry into that trial. * All samples to be studied were obtained and stored as part of CALGB 140202. The material and data obtained from the patient's protocol record will be used to obtain appropriate clinical information. In no instance will the patient be contacted directly. * There should be no physical, psychological, social or legal risks associated with this study. No invasive procedures are recommended or requested. * All appropriate and necessary procedures will be utilized to maintain confidentiality. All patients who have had samples submitted for analysis will have their CALGB study number used to identify specimens. * This study does not require direct patient contact and no specific risk or benefits to individuals involved in the trial are anticipated. It is likely however, that the information gained will substantially help similar patients in the future.