Somatostatin analogs in association with peptide receptor radionucleotide therapy in advanced well-differentiated

Natalie Prinzi1, Alessandra Raimondi1, Marco Maccauro1

  • 1Fondazione IRCCS Istituto Nazionale Tumori Milano, ENETS Center of Excellence, Department of Medical Oncology, Milan, Italy.

Insights

Switching somatostatin analogs (SSAs) after progression in patients with advanced gastroenteropancreatic neuroendocrine tumors treated with peptide receptor radionucleotide therapy improves survival outcomes. This strategy offers better progression-free and overall survival compared to maintaining the same SSA treatment.

Area of Science:

  • Oncology
  • Nuclear Medicine
  • Endocrinology

Background:

  • Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are a heterogeneous group of malignancies.
  • Peptide receptor radionucleotide therapy (PRRT) combined with somatostatin analogs (SSAs) is a standard treatment for advanced GEP-NETs.
  • Treatment failure with SSAs necessitates evaluating alternative therapeutic strategies.

Purpose of the Study:

  • To evaluate the impact of switching somatostatin analogs (SSAs) versus continuing the same SSA after disease progression in patients with advanced well-differentiated GEP-NETs undergoing PRRT.
  • To compare progression-free survival (PFS) and overall survival (OS) between the two treatment strategies.

Main Methods:

  • Retrospective analysis of 69 patients with well-differentiated GEP-NETs treated with PRRT and SSAs.
  • Patients were divided into two groups: S1 (maintained same SSA after progression) and S2 (switched to a different SSA after progression).
  • Progression-free survival and overall survival were the primary endpoints.

Main Results:

  • Median PFS was significantly longer in the switch group (S2: 127 months) compared to the maintain group (S1: 53 months) (p=0.001).
  • Median OS was also significantly improved in the switch group (S2: 150 months) versus the maintain group (S1: 69 months) (p=0.004).
  • Hazard ratios indicated a substantially lower risk of progression and death in the switch group.

Conclusions:

  • Switching to a different somatostatin analog after disease progression, in combination with PRRT, significantly improves both progression-free and overall survival in patients with advanced well-differentiated GEP-NETs.
  • The 'switch' strategy represents a more effective approach compared to continuing the same SSA after progression.
  • This finding supports personalized treatment adjustments in managing advanced GEP-NETs.

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