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.

Abstract

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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