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Systemic Therapy for Tumor Control in Metastatic Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors:
Jaydira Del Rivero1, Kimberly Perez2, Erin B Kennedy3
1Center for Cancer Research, National Cancer Institute, Bethesda, MD.
Purpose:
To develop recommendations for systemic therapy for well-differentiated grade 1 (G1) to grade 3 (G3) metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs).
Methods:
ASCO convened an Expert Panel to conduct a systematic review of relevant studies and develop recommendations for clinical practice.
Results:
Eight randomized controlled trials met the inclusion criteria for the systematic review.
Recommendations:
Somatostatin analogs (SSAs) are recommended as first-line systemic therapy for most patients with G1-grade 2 (G2) metastatic well-differentiated GI-NETs. Observation is an option for patients with low-volume or slow-growing disease without symptoms. After progression on SSAs, peptide receptor radionuclide therapy (PRRT) is recommended as systematic therapy for patients with somatostatin receptor (SSTR)-positive tumors. Everolimus is an alternative second-line therapy, particularly in nonfunctioning NETs and patients with SSTR-negative tumors. SSAs are standard first-line therapy for SSTR-positive pancreatic (pan)NETs. Rarely, observation may be appropriate for asymptomatic patients until progression. Second-line systemic options for panNETs include PRRT (for SSTR-positive tumors), cytotoxic chemotherapy, everolimus, or sunitinib. For SSTR-negative tumors, first-line therapy options are chemotherapy, everolimus, or sunitinib. There are insufficient data to recommend particular sequencing of therapies. Patients with G1-G2 high-volume disease, relatively high Ki-67 index, and/or symptoms related to tumor growth may benefit from early cytotoxic chemotherapy. For G3 GEP-NETs, systemic options for G1-G2 may be considered, although cytotoxic chemotherapy is likely the most effective option for patients with tumor-related symptoms, and SSAs are relatively ineffective. Qualifying statements are provided to assist with treatment choice. Multidisciplinary team management is recommended, along with shared decision making with patients, incorporating their values and preferences, potential benefits and harms, and other characteristics and circumstances, such as comorbidities, performance status, geographic location, and access to care.Additional information is available at www.asco.org/gastrointestinal-cancer-guidelines.
Insights
Systemic therapy recommendations for metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs) favor somatostatin analogs (SSAs) as first-line treatment. Peptide receptor radionuclide therapy (PRRT) is recommended after SSA progression for SSTR-positive tumors.
Area of Science:
- Oncology
- Gastroenterology
- Medical Oncology
Background:
- Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are a heterogeneous group of malignancies.
- Systemic therapy plays a crucial role in managing metastatic GEP-NETs.
- Well-differentiated G1-G3 GEP-NETs require evidence-based treatment guidelines.
Purpose of the Study:
- To establish clinical practice recommendations for systemic therapy in metastatic well-differentiated GEP-NETs (G1-G3).
- To synthesize evidence from randomized controlled trials to guide treatment decisions.
Main Methods:
- An Expert Panel convened by ASCO conducted a systematic review of relevant studies.
- Eight randomized controlled trials met the inclusion criteria for the systematic review.
- Recommendations were developed based on the synthesized evidence.
Main Results:
- Somatostatin analogs (SSAs) are recommended as first-line therapy for most G1-G2 metastatic GI-NETs.
- Peptide receptor radionuclide therapy (PRRT) is recommended after SSA progression for SSTR-positive tumors.
- Chemotherapy, everolimus, or sunitinib are options for SSTR-negative or advanced pancreatic NETs.
Conclusions:
- SSAs are the preferred first-line systemic therapy for most G1-G2 metastatic GI-NETs and SSTR-positive pancreatic NETs.
- PRRT is a recommended second-line option for SSTR-positive tumors progressing on SSAs.
- Treatment decisions for G3 GEP-NETs and SSTR-negative tumors involve chemotherapy, everolimus, or sunitinib, with multidisciplinary input.
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