Study to Nivolumab Following Preoperative Chemoradiotherapy

Inclusion criteria: (A. Phase Ib and Cohorts A and D only) A1. Rectal cancer patients who have not undergone treatment for pre-CRT tumors situated 12 cm or less from the lower edge of the AV. A2. The primary rectal lesion is histopathologically diagnosed as adenocarcinoma. A3. Pre-CRT clinical stage is clinical T3-4 N-any M0. A4. Macroscopic radical resection is deemed possible on pre-CRT image diagnosis. A5. Aged between 20 and 80 years at the time of enrollment. (B. Cohort B only) B1. Clinically diagnosed with local recurrence after rectal surgery. B2. The main site of recurrence is limited to the pelvis by pre-CRT imaging diagnosis. B3. Macroscopic radical resection is deemed possible on pre-CRT imaging diagnosis. B4. Aged between 20 and 75 years at the time of enrollment. (C. Cohort C only) C1. Rectal cancer patients who have not undergone pretreatment for a pre-CRT tumor which is 12 cm or less from the lower AV. C2. The primary rectal lesion is histopathologically diagnosed as adenocarcinoma. C3. The pre-CRT clinical stage is clinical T3-4 N-any M1a (liver) M1a (lungs). C4. Macroscopic curative resection of the primary rectal lesion is deemed possible on pre-CRT imaging diagnosis. C5. A metastatic liver tumor or a metastatic lung tumor has been diagnosed as clinically resectable prior to CRT and during clinical trial enrollment. (D. Common to all cohorts in Phase Ib and Phase II) D1. Patients who have provided consent through a consent form. D2. Patients whose Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) is 0 or 1 at the time of enrollment. D3. CRT was administered: D4. Patients whose CRT adverse events have recovered to Grade 1 or lower based on CTCAE ver.4.0. within 14 days after the end of CRT, and are expected to be able to take nivolumab (patient is still eligible even if adverse events are not restored to Grade 1, provided that the blood cell count satisfies the eligibility criteria specified in point D8). D5. Patients with no remote metastases as confirmed by imaging at the end of CRT (testing is allowed from 14 days before the end of CRT to the trial enrollment date). D6. For women who may become pregnant (including patients who are not menstruating due to chemically-induced menopause among other medical reasons), patients who agree to use contraception for at least 23 weeks after the last administration of the investigational drug, starting from the day they provide consent (30 days (ovulation cycle) plus five times the elimination half-life of the investigational drug). D7. For men, patients who agree to use contraception for at least 31 weeks after the last administration of the investigational drug, starting from the day they provide consent (90 days (spermatogenesis cycle) plus five times the elimination half-life of the investigational drug). D8. Patients who have the sufficient organ function at the time of enrollment. Exclusion criteria 1. Patients diagnosed with active double cancer (synchronous double cancer and double cancer with disease-free period within five years from enrollment). However, lesions equivalent to intraepithelial or mucosal carcinoma deemed cured by localized treatment are not classified as active double cancer. 2. Patients with a history of pelvic irradiation prior to this rectal cancer treatment. 3. Patients who have not given consent through the informed consent form. 4. Patients deemed by the investigator to be ineligible for the trial.