Inclusion Criteria:

          -  Histologically confirmed T1b-T3N0M0 (stage IA-IIB) NSCLC, which have been judged to be
             medically inoperable and will have undergone a course of lung SBRT will be enrolled in
             this trial. Eligible patients who will have completed lung SBRT will have had
             appropriate staging studies identifying them as specific subsets of American Joint
             Committee on Cancer (AJCC) 7th edition stage I or stage II based on only one of the
             following combinations of primary tumor, regional nodes, metastasis (TNM) staging
             using size criteria:

               -  A. T2a (>3cm, < 5cm) N0 M0, Stage IB

               -  B. T2b (>5 cm, < 7cm) N0 M0, Stage IIA

               -  C. T3 (>7cm) N0 M0, Stage IIB

        In order to be eligible for participation in this trial, the subject must:

          -  Be willing and able to provide written informed consent/assent for the trial.

          -  Have measurable or unmeasurable disease based on RECIST 1.1.

          -  Be willing to provide archival tissue from a tumor lesion.

          -  Have a performance status of 0-2 on the Eastern Cooperative Oncology Group (ECOG)
             Performance Scale.

          -  All screening labs should be performed within 10 days of treatment initiation.

               -  Absolute neutrophil count ≥ 1,500/mcL

               -  Platelets ≥ 100,000/mcL

               -  Hemoglobin ≥ 9g/dL or ≥5.6mmol/L without transfusion or erythropoietin dependency
                  (within 7 days of assessment

               -  Serum creatinine ≤ 1.5 times the upper limit of normal (ULN) or measured or
                  calculated creatinine clearance ≥ 60 mL/min for subjects with creatinine levels >
                  1.5 times ULN

               -  Serum total bilirubin ≤ 1.5 times ULN or direct bilirubin ≤ ULN for subjects with
                  total bilirubin levels > 1.5 ULN

               -  aspartate aminotransferase (AST) (SGOT) and Alanine transaminase (ALT) (SGPT) ≤
                  2.5 times ULN or ≤ 5 times ULN for subjects with liver metastases

               -  Albumin ≥ 2.5mg/dL

          -  Female subject of childbearing potential should have a negative urine or serum
             pregnancy within 72 hours prior to receiving the first dose of study medication. If
             the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
             will be required.

          -  Female subjects of childbearing potential must be willing to use an adequate method of
             contraception - Contraception, for the course of the study through 120 days after the
             last dose of study medication.

        Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception
        for the subject.

        - Male subjects of childbearing potential must agree to use an adequate method of
        contraception - Contraception, starting with the first dose of study therapy through 120
        days after the last dose of study therapy.

        Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception
        for the subject.

        Exclusion Criteria:

          -  Has received lung SBRT for stage IA disease, or for any T2 primary tumors involving
             the main bronchus, 2 cm of more distal to the carina; or with associated with
             atelectasis that extends to the hilar region; or for any T3 tumors that invade the
             chest wall, mediastinal pleura, diaphragm, phrenic nerve, parietal pericardium, tumor
             or the main bronchus less than 2 cm distal to the carina; atelectasis of the entire
             lung; or with separate tumor nodule(s) in the same lobe.

          -  Is currently participating and receiving study therapy or has participated in a study
             of an investigational agent and received study therapy or used an investigational
             device within 4 weeks of the first dose of treatment.

          -  Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any
             other form of immunosuppressive therapy within 7 days prior to the first dose of trial
             treatment.

          -  Has a known history of active Bacillus Tuberculosis (TB).

          -  Hypersensitivity to pembrolizumab or any of its excipients.

          -  Has had any prior chemotherapy or targeted small molecule therapy for the currently
             diagnosed cancer.

          -  Has a known additional malignancy that is progressing or requires active treatment.
             Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the
             skin that has undergone potentially curative therapy or in situ cervical cancer.

          -  Has active autoimmune disease that has required systemic treatment in the past 2 years
             (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive
             drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid
             replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
             form of systemic treatment.

          -  Has known history of, or any evidence of active, non-infectious pneumonitis.

          -  Has an active infection requiring systemic therapy.

          -  Has a history or current evidence of any condition, therapy, or laboratory abnormality
             that might confound the results of the trial, interfere with the subject's
             participation for the full duration of the trial, or is not in the best interest of
             the subject to participate, in the opinion of the treating investigator.

          -  Has known psychiatric or substance abuse disorders that would interfere with
             cooperation with the requirements of the trial.

          -  Is pregnant or breastfeeding, or expecting to conceive or father children within the
             projected duration of the trial, starting with the pre-screening or screening visit
             through 120 days after the last dose of trial treatment.

          -  Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

          -  Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).

          -  Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (HCV).

          -  Has received a live vaccine within 30 days of planned start of study therapy. Note:
             Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
             are allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live
             attenuated vaccines, and are not allowed.