Chemotherapy and Radiation Therapy With or Without Metformin Hydrochloride in Treating Patients With Stage III Non-small Cell Lung Cancer

Inclusion Criteria

• •Pathologically (histologically or cytologically) proven diagnosis of stage IIIA or IIIB non-small cell lung cancer within 84 days of registration; eligible histologies include adenocarcinoma, adenosquamous, large cell carcinoma, squamous carcinoma, non-lobar and non-diffuse bronchoalveolar cell carcinoma or non-small cell lung cancer not otherwise specified)
• •Patients must have measurable disease
• •Patients must have unresectable disease, be medically inoperable, or unwilling to undergo surgical management
• •Appropriate stage for protocol entry, including no distant metastases, based upon the following minimum diagnostic workup:
• •* History/physical examination, including documentation of height, weight, body surface area, and vital signs, within 30 days prior to registration
• •* Computed tomography (CT) with IV contrast or magnetic resonance imaging (MRI) imaging (if CT scan with contrast is medically contraindicated) of the lung and upper abdomen through the adrenal glands, required within 45 days prior to registration (recommended within 30 days prior to registration
• •* MRI of the brain with contrast (or CT with contrast if MRI is medically contraindicated) within 45 days prior to registration; note: the use of intravenous contrast is required for the MRI or CT; an MRI without contrast is only permitted if the patient has a contrast allergy
• •* Whole-body fludeoxyglucose (FDG)-positron emission tomography (PET)/CT required within 45 days prior to registration (recommended within 30 days prior to registration; note: patients do not need to have a separate CT of the chest and upper abdomen with contrast if PET/CT imaging includes a high quality CT with contrast
• •Zubrod performance status 0-1
• •Absolute neutrophil count (ANC) \>= 1,500 cells/mm\^3
• •Complete blood count(CBC)/differential obtained within 14 days prior to registration on study, with adequate bone marrow function defined as follows:
• •* Absolute neutrophil count (ANC) ≥ 1,500 cells/mm3
• •* Platelets \>= 100,000 cells/mm\^3
• •* Hemoglobin \>= 8.0 g/dl (note: the use of transfusion or other intervention to achieve hemoglobin \[Hgb\] \>= 8.0 g/dl is acceptable)
• •Adequate renal function within 14 days prior to registration, defined as serum creatinine within normal institutional limits or creatinine clearance must be at least 60 ml/min;
• •Adequate hepatic function within 14 days prior to registration, defined as total bilirubin ≤ 1.5 x upper limit of normal (ULN) for the institution and alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase ≤ 2.5 x ULN for the institution;
• •Fasting blood glucose ≤ 125 mg/dL within 14 days prior to registration;
• •Serum albumin \> 3.0 g/dl within 14 days prior to registration;
• •For women of childbearing potential, a serum pregnancy test within 72 hours prior to registration;
• •Patients with post-obstructive pneumonia are eligible provided they no longer require intravenous antibiotics at registration;
• •Patients must be at least 3 weeks from prior thoracotomy (if performed);
• •If a pleural effusion is present, the following criteria must be met at registration to exclude malignant involvement (incurable M1a disease):
• •* When pleural fluid is visible on both the CT scan and on a chest x-ray, a pleuracentesis is required to confirm that the pleural fluid is cytologically negative;
• •* Effusions that are minimal (i.e. not visible under ultrasound guidance) and that are too small to safely tap are eligible.
• •Women of childbearing potential and male participants must practice adequate contraception throughout the study;