Peptide Receptor Radionuclide Therapy as First-Line Systemic Treatment in Advanced Inoperable/Metastatic

Swayamjeet Satapathy1, Bhagwant Rai Mittal1, Ashwani Sood1

  • 1From the Departments of Nuclear Medicine.

Abstract

Insights

First-line peptide receptor radionuclide therapy (PRRT) with Lu-DOTATATE demonstrated efficacy and safety in advanced neuroendocrine tumors (NETs). This treatment offers a promising option for patients with inoperable or metastatic NETs, showing significant progression-free survival.

Area of Science:

  • Oncology
  • Nuclear Medicine
  • Radiopharmaceutical Therapy

Background:

  • Advanced inoperable/metastatic neuroendocrine tumors (NETs) present significant therapeutic challenges.
  • Limited treatment options exist for advanced NETs, necessitating novel therapeutic strategies.
  • Peptide receptor radionuclide therapy (PRRT) targets somatostatin receptors, offering a specific approach for NETs.

Purpose of the Study:

  • To evaluate the efficacy and safety of PRRT as a first-line systemic therapy for advanced inoperable/metastatic NETs.
  • To assess the treatment response and progression-free survival in NET patients receiving first-line PRRT.

Main Methods:

  • Retrospective analysis of consecutive patients with advanced inoperable/metastatic NETs treated with first-line Lu-DOTATATE and capecitabine.
  • Treatment involved Lu-DOTATATE cycles combined with capecitabine over a defined period.
  • Radiological response was assessed using Response Evaluation Criteria in Solid Tumors version 1.1.

Main Results:

  • A partial response was observed in 30% of patients, with 55% achieving stable disease.
  • Disease progression was noted in only 15% of patients, indicating significant disease control.
  • Treatment-related adverse effects were minimal, with low rates of grade 3/4 hematological and hepatic toxicity.

Conclusions:

  • First-line PRRT with Lu-DOTATATE is an effective and safe treatment option for advanced NETs.
  • The study highlights a median progression-free survival of 48 months.
  • Further randomized trials comparing PRRT with somatostatin analogs are needed to establish optimal treatment sequencing.