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Published on: September 24, 2020
Pancreatic neuroendocrine tumors: does chemotherapy work?
Mohamedtaki Abdulaziz Tejani1, Muhammad Wasif Saif
1Division of Hematology and Oncology, University of Rochester. Rochester, NY, USA. mohamed_tejani@urmc.rochester.edu.
Combination capecitabine and temozolomide shows promise for advanced pancreatic neuroendocrine tumors (pNETs). This regimen may offer a new option for patients with metastatic pNET, addressing limitations of current treatments.
Area of Science:
- Oncology
- Gastroenterology
- Medical Oncology
Background:
- Pancreatic neuroendocrine tumors (pNETs) are rare neoplasms with variable prognosis.
- Current treatments for advanced, unresectable pNETs include somatostatin analogs, everolimus, and sunitinib.
- Existing systemic therapies have limitations in response rates and toxicity, necessitating novel treatment strategies.
Framework:
- This review focuses on three abstracts presented at the 2014 ASCO Gastrointestinal Cancers Symposium.
- The abstracts evaluate the efficacy and safety of combination capecitabine and temozolomide therapy.
- The study population comprises patients with advanced, unresectable pancreatic neuroendocrine tumors.
Implementation:
- Combination capecitabine and temozolomide was administered to patients with advanced pNET.
- Outcomes such as response rates, progression-free survival, and toxicity were assessed.
- Data from the three abstracts were summarized to provide a comprehensive overview.
Implications:
- The combination of capecitabine and temozolomide demonstrates potential as a treatment option for advanced pNET.
- This regimen may represent a valuable addition to the treatment algorithm for metastatic pNET.
- Further investigation into this combination therapy is warranted to optimize its role in clinical practice.
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