Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Inclusion Criteria: * Subjects must have histologically or cytologically confirmed non-small cell lung cancer (NSCLC) or neuroendocrine carcinoid tumor * All subjects must have one of the following stages: Stage IA(T1NO); IB (T2NO), II \& IIIA (N2 negative); IIIA (N2+), IIIB (N3+) * Patients must have stable disease at the time of enrollment * Women and men at least 18 years of age * ECOG performance status 0-1(Appendix A) * Subjects must be within 4 to 24 weeks of standard of care treatment for their particular stage of disease * Subjects must have acceptable organ and marrow function as defined below: * Leukocytes \> 3,000/µL * Absolute Neutrophils \> 1,500/µL * Hemoglobin \> 10 g/dL * Platelets \> 100,000/µL * Total Bilirubin within normal institutional limits * Creatinine within normal institutional limits OR * Creatinine clearance \> 60 mL/min/1.73 m2 for subjects with above normal AST and ALT with alkaline phosphatase within \< 1.5 times upper limit of normal * The effects of a MUC1vaccine on the developing human fetus at the recommended therapeutic dose are unknown. For this reason, men and women of childbearing potential must be willing to use effective contraception (hormonal barrier method of birth control; abstinence) while on study treatment and for at least 3 months thereafter. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately Exclusion Criteria: * Su…