Efficacy of Rechallenge With Sunitinib in Metastatic Pancreatic Neuroendocrine Tumor Previously Failed to Sunitinib

Inclusion Criteria: * Subjects \> 18 years old and able to give their informed consent. * Patients diagnosed with Neuroendocrine Tumor of pancreatic origin and histologically confirmed, G1/2 according to the World Health Organization (WHO) classification (Ki67 \<20% and/or mitotic count \>20 mitoses x 10 HPF). * Metastatic disease progression in the 12 months prior to baseline visit documented by CT, MRI or Octreoscan. * Progression to prior treatment with sunitinib administered for metastatic disease and have received at least 1 line and no more than 2 lines of subsequent systemic treatment. * Measurable disease according to the following criteria RECIST version 1.1 * No disease that can be treated with surgery, radiotherapy or combined treatment with curative intent. * Eastern Cooperative Oncology Group (ECOG) 0-2. * Pretreatment with somatostatin analogues, chemotherapy, anti-VEGF (vascular endothelial growth factor) and mTOR (mammalian target of rapamycin) inhibitors prior to participation in the study is allowed. * Adequately controlled blood pressure (BP) \<150/90 mmHg. * Hematologic Function: - Absolute neutrophil count \>1500 / microliter (uL) - Platelets \>100,000 / uL - Hemoglobin \>5.6 mmol / L (9 g / dL) * Liver function: total bilirubin \< 1.5 x upper limit of normal (ULN), unless unconjugated hyperbilirubinemia or Gilbert syndrome. - Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \< 2.5 x ULN (\< 5 times in case of liver metastases). * Renal function: calculated creatinine clearance according to Cockcroft-Gault \> 30 ml / min. * Blood coagulation: prothrombin time (PT) or International Normalized Ratio (INR) \< 1.2 x ULN. * Proteinuria \<2+ urine dipstick. If \> 2+ proteinuria, urinary protein \<1 g / 24 h. * Life expectancy\> 3 months. * Patient able to swallow the study drug and comply with the monitoring requirements of the study. - Women of childbearing potential must present a negative pregnancy test. Women of childbearing potential must agree to use contraception. * Men whose partners are women of childbearing potential must use effective contraception. Exclusion Criteria: * Neuroendocrine tumors of pancreatic origin G3 according to WHO classification. * Patients who received 3 or more lines of systemic treatment. * Major surgery or trauma within 4 weeks prior to the first dose of sunitinib. * Radiation therapy or tumor embolization within 2 weeks prior to the first dose of sunitinib. * Chemotherapy, immunotherapy, biologic therapy or investigational therapy within the previous 2 weeks or 5 half-lives of the drug last received before the start of the first dose of sunitinib treatment. * Prior treatment with high-dose chemotherapy that required hematopoietic rescue. * Immunosuppressive therapy or prolonged treatment with corticosteroids concomitantly administered in the previous 3 months. * Resolution to grade \<2 (CTCAE according V4.03) of all previous related toxicities except alopecia treatments. * Any ongoing toxicity from prior anti-cancer therapy that is \>Grade 1 (according CTCAE V4.03) and/or that is progressing in severity, except alopecia. * Treatment with potent inhibitors or inducers of CYP3A4 or known to prolong the QT interval in the previous 7 days. * Prior radiotherapy to more than 25% of the bone marrow - Presence of uncontrolled metastatic brain disease, spinal cord compression, meningeal carcinomatosis or leptomeningeal disease. * Any gastrointestinal malabsorption disorder or any other condition that, at investigator's criteria, may affect the absorption of sunitinib or increase the risk of bleeding or perforation. * Presence of any non-healing wound or ulcer. * Grade III/IV diarrhea in the screening period. * Diagnosis of any second malignancy within the last 5 years, except for adequately treated basal cell or squamous cell skin cancer, or in situ carcinoma of the cervix uteri. * Clinically significant cardio/cerebrovascular disease in the 6 months prior to treatment. * Cardiac arrhythmias (NCI CTCAE version 4.0 grade \>2), atrial fibrillation of any grade that requires medical treatment. * Corrected QT interval (QTcF) \> 180 msec. * Active hemoptysis in the past 6 weeks. * Evidence of active bleeding or bleeding diathesis. * Presence of endobronchial lesions and/or lesions that infiltrate large vessels. * Current treatment with acenocoumarol at therapeutic doses. * Known HIV infection. * Presence of uncontrolled active infection. * Pregnant or breastfeeding women. * Previous allergic reaction to components structurally similar to sunitinib or any of the excipients. * Inability to discontinue any prohibited concomitant medication. * Any illness (medical or psychiatric) or reason, in the investigator's opinion, that interferes with the patient's ability to participate.