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Updated: May 12, 2026

A Practical Guide for the Production and PET/CT Imaging of 68Ga-DOTATATE for Neuroendocrine Tumors in Daily Clinical Practice
Published on: April 17, 2019
Digestive neuroendocrine tumors (DNET): the era of targeted therapies
Tarek Boussaha1, Philippe Rougier, Julien Taieb
1Service d'hépatogastroentérologie, Groupement Hospitalier Pitié-Salpêtrière, Paris, France.
Abstract:
Neuroendocrine tumors (NETs) are a heterogeneous group of malignancies. Therapeutic options depend on location of the primitive tumor, its expandability, its hormonal symptoms and its differentiation. Though relatively rare, with an increasing incidence and a high prevalence digestive neuroendocrine tumors (DNETs) are ranked just behind colorectal cancer as the most common digestive cancers in developed countries. Three main therapeutic axes have been individualized in the field of well-differentiated DNETs (corresponding to grades 1 and 2 of new WHO classification 2010), firstly, antitumor activity of somatostatin analogs, particularly in slowly progressive metastatic DNETs with limited hepatic invasion, secondly, targeting angiogenesis in these hypervascular tumors and thirdly targeting the mTOR pathway involved in DNETs carcinogenesis. As a consequence of two major randomized phase III trials in 2011, sunitinib and everolimus have been considered as new therapeutic options for well-differentiated, advanced and progressive pancreatic NETs. For everolimus, another phase III study, although non-significant with the chosen criteria, showed effectiveness notably against small intestine NETs. These targeted therapies are new therapeutic weapons in management of well-differentiated DNETs, but its exact role in care strategy, in comparison with other treatments (somatostatin analogs, chemo-embolization, chemotherapy...) deserves to be precise in the future.
Insights
Digestive neuroendocrine tumors (DNETs) are increasingly common. New targeted therapies like sunitinib and everolimus offer new options for advanced DNETs, though their precise role requires further study.
Area of Science:
- Oncology
- Gastroenterology
- Endocrinology
Background:
- Digestive neuroendocrine tumors (DNETs) are a significant and growing cause of digestive cancers.
- Therapeutic strategies for DNETs are tailored to tumor location, grade, and hormonal activity.
- Well-differentiated DNETs (WHO grades 1 and 2) have specific therapeutic axes including somatostatin analogs, anti-angiogenesis, and mTOR pathway targeting.
Purpose of the Study:
- To review current and emerging therapeutic options for well-differentiated DNETs.
- To highlight the impact of recent phase III trials on treatment strategies.
- To discuss the potential role of targeted therapies in the management of DNETs.
Main Methods:
- Review of major randomized phase III clinical trials.
- Analysis of therapeutic axes for well-differentiated DNETs.
- Evaluation of targeted therapies such as sunitinib and everolimus.
Main Results:
- Sunitinib and everolimus are established options for advanced, progressive pancreatic NETs.
- Everolimus demonstrated effectiveness in small intestine NETs, though not reaching statistical significance in all criteria.
- Somatostatin analogs remain important for slowly progressive metastatic DNETs with limited hepatic invasion.
Conclusions:
- Targeted therapies represent significant advancements in managing well-differentiated DNETs.
- Further research is needed to define the optimal place of these novel agents within the broader DNET treatment landscape.
- Comparative studies are essential to elucidate the precise role of targeted therapies against established treatments like chemotherapy and embolization.
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