Commentary|Podcasts|January 7, 2026

PRRT With 177Lu-Edotreotide Improves Outcomes vs Everolimus in Metastatic GEP-NETs: With Jonathan R. Strosberg, MD

Fact checked by: Jax DiEugenio

Jonathan R. Strosberg, MD, reviews the clinical implications of PRRT with 177Lu-edotreotide for metastatic gastroenteropancreatic neuroendocrine tumors.

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In today’s episode, the discussion features Jonathan R. Strosberg, MD, a professor and leader in the Neuroendocrine Tumor Division and the Department of Gastrointestinal Oncology Research Program at Moffitt Cancer Center in Tampa, Florida, who reviewed the clinical implications of peptide receptor radionuclide therapy (PRRT) with 177Lu-edotreotide (ITM-11) for patients with metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs), drawing on efficacy and safety findings from the phase 3 COMPETE trial (NCT03049189).

In our exclusive interview, Dr Strosberg contextualized 177Lu-edotreotide as a PRRT approach that is mechanistically similar to lutetium Lu 177 dotatate (Lutathera) but uses a different somatostatin analog vector. He also emphasized the relevance of COMPETE as a head-to-head comparison of lutetium-based PRRT vs an active standard option everolimus (Afinitor) in this setting. He summarized key efficacy signals, including an improvement in progression-free survival and higher response rates with PRRT vs everolimus, and discussed subgroup trends by grade, primary site, and line of therapy. He also highlighted practical takeaways relevant to real-word clinical practice.

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