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Emerging Treatment Options for Gastroenteropancreatic Neuroendocrine Tumors
Mauro Cives1,2, Eleonora Pelle'1, Jonathan Strosberg3
1Department of Biomedical Sciences and Human Oncology, University of Bari, 70124 Bari, Italy.
Abstract:
Treatment options for neuroendocrine tumors (NETs) and carcinomas (NECs) are expanding. Early-phase studies have shown preliminary evidence of the antitumor activity of alpha-emitting peptide receptor radionuclide therapy (PRRT), and novel radiopeptides incorporating somatostatin receptor antagonists (rather than agonists) have been developed. Several tyrosine kinase inhibitors (TKIs) with antiangiogenic potential have been evaluated in patients with NETs, including lenvatinib, axitinib, cabozantinib and pazopanib. Recently, two phase 3 clinical trials have demonstrated the efficacy and safety of surufatinib, an inhibitor of vascular endothelial growth factor receptor (VEGFR)-1, -2, -3, fibroblast growth factor receptor (FGFR)-1 and colony stimulating factor-1 receptor (CSF-1R), in patients with pancreatic and extra-pancreatic NETs. Multiple clinical trials of combination immunotherapy have been recently completed, but interpretation of the results is hampered by small samples sizes and discordant outcomes. This review summarizes recent data on emerging treatments for neuroendocrine neoplasms.
Insights
Emerging treatments for neuroendocrine neoplasms (NENs) are expanding, including novel peptide receptor radionuclide therapy and tyrosine kinase inhibitors. Surufatinib shows efficacy in pancreatic and extra-pancreatic NENs, while immunotherapy trials yield mixed results.
Area of Science:
- Oncology
- Medical Science
Background:
- Treatment options for neuroendocrine tumors (NETs) and carcinomas (NECs) are rapidly evolving.
- Early research indicates potential for alpha-emitting peptide receptor radionuclide therapy (PRRT) and somatostatin receptor antagonists.
Purpose of the Study:
- To review recent advancements in emerging treatments for neuroendocrine neoplasms (NENs).
- To summarize data on novel therapeutic strategies including PRRT, tyrosine kinase inhibitors, and immunotherapy.
Main Methods:
- Review of early-phase studies and late-phase clinical trials.
- Evaluation of novel radiopeptides and targeted therapies like tyrosine kinase inhibitors (TKIs).
- Analysis of clinical trial data for surufatinib and combination immunotherapies.
Main Results:
- Preliminary evidence supports antitumor activity of alpha-emitting PRRT and novel radiopeptides.
- Several TKIs (lenvatinib, axitinib, cabozantinib, pazopanib) show antiangiogenic potential in NETs.
- Surufatinib demonstrated efficacy and safety in phase 3 trials for pancreatic and extra-pancreatic NETs; immunotherapy results are mixed.
Conclusions:
- The landscape of NEN treatment is expanding with promising new therapeutic avenues.
- Targeted therapies like surufatinib and TKIs, along with PRRT, represent significant progress.
- Further research is needed to clarify the role of combination immunotherapy in NEN management.
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